- We are sorry, but NCBI web applications do not support your browser and may not function properly. More information

- Journal List
- Genetics
- v.171(1); 2005 Sep
- PMC1456515

# Functional Mapping of Quantitative Trait Loci That Interact With the *hg* Mutation to Regulate Growth Trajectories in Mice

^{*}Department of Statistics, University of Florida, Gainesville, Florida 326111 and

^{†}Department of Animal Science, University of California, Davis, California 95616

^{1}

*Corresponding author:*Department of Statistics, 533 McCarty Hall C, University of Florida, Gainesville, FL 32611. E-mail: ude.lfu.tats@uwr

## Abstract

The high growth (*hg*) mutation increases body size in mice by 30–50%. Given the complexity of the genetic regulation of animal growth, it is likely that the effect of this major locus is mediated by other quantitative trait loci (QTL) with smaller effects within a web of gene interactions. In this article, we extend our functional mapping model to characterize modifier QTL that interact with the *hg* locus during ontogenetic growth. Our model is derived within the maximum-likelihood context, incorporated by mathematical aspects of growth laws and implemented with the EM algorithm. In an F_{2} population founded by a congenic high growth (HG) line and non-HG line, a highly additive effect due to the *hg* gene was detected on growth trajectories. Three QTL located on chromosomes 2 and X were identified to trigger significant additive and/or dominant effects on the process of growth. The most significant finding made from our model is that these QTL interact with the *hg* locus to affect the shapes of the growth process. Our model provides a powerful means for understanding the genetic architecture and regulation of growth rate and body size in mammals.

THE high growth (*hg*) gene is a spontaneous mutation that results in a 30–50% increase in postnatal body growth in mice (Bradford and Famula 1984). Earlier physiological studies suggest that the increase of growth efficiency by the *hg* locus stems from increased energy metabolism without altering overall body composition (Calvert *et al.* 1985, 1986). Using an interval-mapping approach (Lander and Botstein 1989), Horvat and Medrano (1995) have localized the *hg* locus near Dl0Mit41 on the distal half of mouse chromosome 10 in both female and male F_{2} populations. These authors further found that the *hg* phenotype is the result of a 500-kb deletion in chromosome 10 that includes three genes, suppressor of cytokine signaling-2 (*Socs*2), CASP2 and RIPH1 domain containing adaptor with death domain (*Raidd*/*cradd*), and viral encoded semaphorin receptor (*Vespr* or *Plexin C*1) (Wong *et al.* 2002). The HG phenotype results from the lack of expression of *Socs*2 (Horvat and Medrano 2001), which regulates growth hormone signal transduction.

Given the genetic complexity of growth, it is unlikely that the *hg* gene triggers a marked effect on growth rate and body size with no mediation by environment and other loci. As observed by Corva and Medrano (2000), for example, the nutritional environment confounds the expression of the *hg* effect on the high growth phenotype in mice. To identify modifiers of the *hg* locus, Corva *et al.* (2001) developed an F_{2} population segregating for *hg* to examine interactions between *hg* and other growth genes. They identified a significant quantitative trait locus (QTL), *Q*2*Ucd*2, located on chromosome 2, affecting weight gain from 2–9 weeks. This QTL accounts for 10.4% of the phenotypic variance in the homozygous *hg*/*hg* mice and also exerts effects on carcass ash and protein and femur length.

Comparing two F_{2} subpopulations, one homozygous for the mutant allele (*hg*/*hg*) and the other homozygous for the wild-type allele (+/+), Corva *et al.* (2001) detected a growth QTL that was expressed differently between the two subpopulations and, therefore, thought to interact with the *hg* locus. Such an *hg* background-dependent QTL identified from single-trait mapping makes it worthwhile to perform more thorough QTL analyses for ontogenetic growth using functional mapping (Ma *et al.* 2002; Wu *et al.* 2004a,b,c; Zhao *et al.* 2004). Functional mapping that integrates mathematical aspects of growth laws into a mapping framework can localize dynamic QTL responsible for the biological process of a trait measured at a finite number of time points and provide biologically meaningful results about QTL detection. By estimating the parameters that determine shape and function of a particular biological process, rather than directly estimating gene effects at all possible points during the entire time course, functional mapping strikingly reduces the number of parameters to be estimated and, hence, displays increased statistical power to detect hidden QTL for growth processes.

The motivation of this article is to develop a statistical model for detecting QTL that interact with the *hg* locus to influence the growth process within the context of functional mapping. Unlike single time point analyses by Corva *et al.* (2001), this model provides a quantitative and testable framework for studying the interplay between epistasis and growth pattern. Also, unlike our earlier interaction model for a pair of unknown QTL (Wu *et al.* 2004a), this model attempts to detect epistasis between modifier QTL and a known gene on the genome, which is supposed to provide better estimates of the QTL locations. Although motivated to solve a practical problem in mouse QTL mapping (Corva *et al.* 2001), we have developed a general epistasis-detecting model that can be used to unveil the genetic secrets of growth trajectories for other species.

## MODEL

### Background and problem:

The *hg* mutation has been introgressed into the C57BL/6J (C57) background through nine backcrosses to create congenic line C57BL/6J-*hg*/*hg* (HG). A mapping population was founded by mating smaller CAST/EiJ (CAST) males to HG females, which produced a total of 75 F_{1} and 1132 F_{2} mice (Corva *et al.* 2001). To test the segregation of *hg* in the mapping population, these F_{2} mice were genotyped by using D10Mit41 on chromosome 10, detected to be linked with *hg* and D10Mit69, a marker that maps within the *hg* deletion (Horvat and Medrano 1995). Mice homozygous for HG alleles at D10Mit41 and without a PCR amplification product for D10Mit69 (indicating homozygosity for the *hg* deletion) were thought to be homozygous for the mutant allele (expressed as *hg*/*hg*). On the other hand, mice homozygous for CAST alleles at D10Mit41 and amplifying for D10Mit69 were regarded as being homozygous for the wide-type allele (expressed as +/+). It was found that there were 274 +/+ mice, 596 +/*hg* mice, and 262 *hg*/*hg* mice in the F_{2} cross, which conforms to Mendelian segregation ratios.

Our hypothesis is that there exist particular QTL for body growth that are expressed differently among the three *hg*-typical genotypes. Such QTL are thought to be modifiers that epistatically modulate the effects of *hg*. Below, we modify our functional mapping model (Ma *et al.* 2002; Wu *et al.* 2004a,c) to detect QTL modifiers that display epistatic effects with the *hg* locus on growth trajectories.

### The likelihood function:

Suppose there are *n* mice for the F_{2}, which is composed of three subpopulations for the *hg* gene with size *n _{j}* (

*j*= 2 for genotype

*hg*/

*hg*, 1 for genotype

*hg*/+, and 0 for genotype +/+). Assume that a QTL for growth curves or trajectories is segregating to form three genotypes, expressed by

*k*(

*k*= 2 for

*Q*from the HG parent and

*q*from the CAST parent. Consider a genetic linkage map constructed for the F

_{2}using molecular markers. The foundation of interval QTL mapping is laid on the mixture model in which each F

_{2}individual is assumed to arise from one and only one of the possible QTL genotypes within known genotypes of two markers that bracket the QTL (Lander and Botstein 1989). The frequencies of each QTL genotype within marker interval genotypes,

*i.e.*, the conditional QTL genotype probabilities given markers (see Table 1), are embedded within the mixture model to reflect the genomic position of the QTL within the marker interval.

**Conditional probabilities (**M

_{k|i}) of QTL genotypes given marker genotypes for**M**

_{}and

_{+1}in the F_{2}populationLet _{k(j)|i} be the conditional probability of a joint *hg*-QTL genotype for individual *i* given a marker genotype. The likelihood function of growth data, **y**, measured at *T* different time points for the *hg* gene and putative QTL is written as

where is the parameter for QTL position contained in the matrix of the QTL conditional probability, **u** contains the genotypic mean vector for different *hg*-QTL genotypes, and **Σ** is the residual covariance matrix within *hg*-QTL genotypes. Equation 1 can be converted to Equation 2 because for each individual the *hg* genotype is known and, thus, the product of the likelihood over different individuals is made among three different *hg* genotypes. In Equation 2, nine joint *hg*-QTL genotypes in the mixture model for a given individual *i* can be simply expressed by three QTL genotypes separately for three *hg* genotypes. For this reason, _{k(j)|i} can be expressed by _{k|i}. We assume that the residual covariance matrix is different among the *hg* genotypes but the same within different QTL genotypes (see Equation 2).

The conditional probability _{k|i} can be differently calculated when the QTL and *hg* are located at different marker intervals and when they are located next to each other. In the former case, _{k|i}'s have the same form for each of the three *hg* genotypes (see Table 1). In the latter case, _{k|i}'s have different forms for different *hg* genotypes, but they still can be obtained from Table 1 by treating the *hg* gene as a marker. The choice of one of the two flanking markers **M**_{} and **M**_{+1} in Table 1 as the *hg* gene depends on the left or right side of the *hg* gene at which the QTL is located.

In the mixture model of Equation 2, the multivariate normal distribution of *hg*-QTL genotype *jk* for growth traits measured for individual *i* in each subpopulation *k* is expressed as

where **y**_{i(j)} = [*y _{i}*

_{(j)}(1),…,

*y*

_{i}_{(j)}(

*T*)] is a vector of subpopulation-specific observation measured at

*T*time points, and

**u**

_{k(j)}= [

*u*

_{k}_{(j)}(1),…,

*u*

_{k}_{(j)}(

*T*)] is a vector of expected values for genotype

*jk*at different points. At a particular time

*t*, the relationship between the observation and expected genotypic value can be described by a linear regression model,

where *x _{ij}* is the indicator variable denoted as 1 if a QTL genotype

*k*is considered for subject

*i*and 0 otherwise; and

*e*

_{i}_{(j)}(

*t*) is the residual error that is i.i.d. normal with the mean of zero and the variance of . The errors at two different time points,

*t*

_{1}and

*t*

_{2}, are correlated with the covariance of cov

_{j}(

*t*

_{1},

*t*

_{2}). These (co)variances compose a (

*T*×

*T*) matrix

**Σ**

_{j}.

### Modeling the mean vector and (co)variance matrix:

The estimation of the mean vector **u**_{k(j)} and the (co)variance matrix **Σ**_{j} is statistically difficult because they involve too many unknown parameters given a possible sample size. Also, such direct estimation does not take into account the biological principles of growth and development. We incorporate the universal growth law, as described by a logistic equation, into the estimation process of the likelihood function (Equation 2). Thus, the mean value of *hg*-QTL genotype *jk* at time *t* is expressed by

where the growth parameter set describes the asymptotic growth, initial growth, and relative growth rate, respectively. With this growth equation, we need only estimate the growth parameters, rather than estimate genotypic values at every point, to detect genotypic differences in growth. This can significantly reduce the number of unknown parameters to be estimated, especially when the number of time points is large. Moreover, the statistical significance of a QTL and its interaction with the *hg* gene can be tested by comparing these growth parameters among the three different QTL genotypes across different subpopulations.

Similarly, the covariance matrix can be structured with an appropriate model. Statistical analysis of longitudinal data has established a number of structural models that capture most of the information contained in the matrix (Diggle *et al.* 2002). Here, we use a first-order autoregressive [AR(1)] model to model the structure of the matrix, which is based on two assumptions, first, the variance σ^{2} is constant over time, and, second, the correlation decays in a proportion of ρ purely with time interval. With the AR(1) model, we need only estimate instead of all elements in the matrix. The advantage of such a matrix-structuring model is to reduce the number of unknown parameters, without losing the information of the matrix. Many other structural models may be more advantageous over the stationary AR(1) model, but the choice of an optimal model in a particular situation should be based on statistical tests, as described in Kirkpatrick and Heckman (1989), Pletcher and Geyer (1999), Zimmerman and Nunez-Anton (2001), and Pletcher and Jaffrezic (2002).

### Computational algorithms:

As classified above, the unknown parameters that build up the likelihood function (Equation 2) include the curve parameters, matrix-structuring parameters, and the QTL genotype frequencies specified by QTL position measured in terms of the recombination fractions (*r*_{1} or *r*_{2}) between the QTL and its flanking markers (see Table 1). Arrayed by , these unknowns can be estimated through differentiating the log-likelihood function of Equation 2 with respect to each unknown, setting the derivative equal to zero, and solving the log-likelihood equations. This estimation process can be implemented with the expectation-maximization (EM) algorithm (Dempster *et al.* 1977) as described below.

The log-likelihood function of growth and marker data () for subpopulation *k* based on Equation 1 is given by

with the derivative with respect to any element Ω_{l}

where we define

which could be thought of as a posterior probability that progeny *i* with a particular marker genotype has QTL genotype *j*. We then implement the EM algorithm with the expanded parameter set {**Ω**, **Π**}, where **Π** = {Π_{k|i}}. Conditional on **Π** (the E step; Equation 4), we solve for

to get the estimates of **Ω** (the M step; Equation 5). The estimates are then used to update **Π**, and the process is repeated between Equations 4 and 5 until convergence. The values at convergence are the maximum-likelihood estimates (MLEs) of **Ω**. The iterative expressions of estimating **Ω** from the previous step were given in Ma *et al.* (2002) and Wu *et al.* (2002, 2004b). In Wu *et al.* (2002), approximate estimates of the samplings errors from Fisher's information matrices were given.

As usual, the QTL position parameter can be viewed as a known parameter because a putative QTL can be searched at every 1 or 2 cM on a map interval bracketed by two markers throughout the entire linkage map. The amount of support for a QTL at a particular map position is often displayed graphically through the use of likelihood maps or profiles, which plot the likelihood-ratio test statistic as a function of map position of the putative QTL.

### Hypothesis tests:

Different from traditional mapping approaches, our functional mapping for longitudinal traits allows for the tests of a number of biologically meaningful hypotheses (Wu *et al.* 2004a). These hypothesis tests can be a *global* test for the existence of significant QTL, a *local* test for the genetic effect on growth at a particular time point, a *regional* test for the overall effect of QTL on a particular period of growth process, or an *interaction* test for the change of QTL expression across times. These tests at different levels can be formulated to test the effects of QTL × *hg* interaction on the shape of growth.

Testing whether specific QTL exist to affect growth trajectories is a first step toward the understanding of the genetic architecture of growth and development. The genetic control over entire growth processes can be tested by formulating the following hypotheses:

The H_{0} states that there are no QTL affecting growth trajectories and the three genotypic curves in each subpopulation overlap (the reduced model), whereas the H_{1} proposes that such QTL do exist (the full model). The test statistic for testing the hypotheses in Equation 6 is calculated as the log-likelihood ratio of the reduced to the full model,

where and denote the MLEs of the unknown parameters under H_{0} and H_{1}, respectively. The LR is asymptotically χ^{2}-distributed with 18 d.f. An empirical approach for determining the critical threshold is based on permutation tests, as advocated by Churchill and Doerge (1994). By repeatedly shuffling the relationships between marker genotypes and phenotypes, a series of the maximum log-likelihood ratios are calculated, from the distribution of which the critical threshold is determined.

After a significant QTL is detected, the next test is about the interaction effect between this QTL and *hg* on growth. We use the area under curve (*A _{k}*

_{(j)}) as a criterion for this QTL ×

*hg*interaction test, expressed as

In this case, the null hypothesis for testing QTL × *hg* interaction can be formulated as

*i.e.,* the difference between the areas under curves of different QTL genotypes is set equal for the three *hg* genotypes.

In addition to testing overall genetic effects on growth trajectories, our model allows for the tests of the additive and dominant effects as well as the interaction effects between the QTL and *hg* locus. Let *a*_{1} and *a*_{2} be the additive effects of the *hg* and QTL; *d*_{1} and *d*_{2} be the dominant effect of the *hg* and QTL; and *I*, *J*, *K*, and *L* be the additive × additive, additive × dominant, dominant × additive, and dominant × dominant epistatic effects between the loci (Lynch and Walsh 1998). We tabulate *A _{k}*

_{(j)}in terms of their genetic compositions as

where *A* is the overall mean. Hypothesis tests for these genetic effects are formulated with constraints

for the additive genetic effects of the *hg* and QTL, respectively,

for the dominant genetic effects of the *hg* and QTL, respectively, and

for the additive × additive, additive × dominant, dominant × additive, and dominant × dominant genetic effect interactions between the *hg* and QTL, respectively.

## RESULTS

To detect QTL modifiers, we need to genotype and phenotype F_{2} mice from each of the three *hg* genotypes *hg*/*hg*, *hg*/+, and +/+. However, the animal material available to our QTL analysis contains only two subpopulations *hg*/*hg* and +/+ developed by Corva *et al.* (2001) with a two-step approach as follows: In the first step, a linkage map covering the 19 autosomes and one sex chromosome (X) was constructed with 83 molecular markers for 262 *hg*/*hg* mice from the F_{2} cross. A simple analysis of variance approach was used to detect significant markers associated with growth rate and body weight. In the second step, the most significant markers genotyped in the *hg*/*hg* subpopulation were also typed for the 274 +/+ mice from the same F_{2} population. These genotyped markers were found to be located at chromosomes 1, 2, 4, 9, and X (Corva *et al.* 2001), with which a common linkage map that integrates the two subpopulations was constructed.

Both the *hg*/*hg* and +/+ subpopulations were phenotyped for body weight on a weekly basis from 2 to 9 weeks of age. However, about one-third of the mice from each subpopulation were measured only at weeks 3, 6, and 9. Although our original model was designed for the same measurement schedule for all subjects (Ma *et al.* 2002), a recent model has been derived to handle subject-dependent measurement schedules with a reasonable convergence rate (Hou *et al.* 2005). Data for body weights at different ages were corrected for the effects of dam, litter, sex, and parity.

The logistic curve described by Equation 3 was used to fit the growth trajectory for each mouse, using nonlinear least-squares approaches. Statistical tests indicate a good fitness at the significance level *P* < 0.001. There is a substantial difference in growth pattern between the two F_{2} subpopulations, *hg*/*hg* and +/+ (Figure 1). On average, these two subpopulations are similar from birth to age 3 weeks, but after 3 weeks the *hg*/*hg* mice display much greater growth (Figure 1B) than do the +/+ mice (Figure 1A). Substantial variation in growth curve among different animals in each subpopulation suggests that specific QTL may be involved in shaping developmental trajectories.

*vs.*ages for (A) 2

*xx*+/+ mice and (B) 2

*xx hg*/

*hg*mice in an F

_{2}progeny derived from HG and CAST lines (Corva

*et al.*2001).

Our mapping model is employed to search for growth QTL through a genome-wide scanning approach. Figure 2 illustrates the profile of the log-likelihood ratio (LR) test statistics throughout the common linkage map for the two subpopulations. The “genome-wide” critical threshold value throughout the common linkage map at the α = 0.01 significance level was estimated as 155.2 on the basis of 1000 permutation tests. According to this criterion, two separate QTL each corresponding to a peak of the LR profile were detected on chromosome X. We also computed the chromosome-wide critical thresholds with the LR peaks of individual chromosomes. A few distinct peaks on chromosome 2 may carry multiple QTL according to this criterion. On the basis of earlier studies with the same mapping material, the locations of these suggestive QTL (Figure 2) contain important QTL for many growth-related traits (Corva *et al.* 2001). For this reason, we perform an in-depth hypothesis test for the QTL located at the highest peak (Figure 2), as for the two QTL on chromosome X.

**...**

The three growth curves each determined by a genotype at each of these significant QTL are drawn separately for the *hg*/*hg* and +/+ mice (Figure 3), using the MLEs of curve parameters (; Table 2) from our model. As expected, the *hg* locus displays a striking (additive) effect on growth trajectories (Table 3). The growth trajectories of the same QTL genotype are different between the two subpopulations, suggesting that the genetic expression of QTL is affected by genetic background. In general, the three detected QTL start to exert their effects on growth in both subpopulations when the mice are 3 weeks of age (Figure 4). After this age, the QTL effects tend to increase with age.

*hg*/

*hg*(red) and +/+ (blue) mice at the QTL, detected by our joint model, on chromosomes 2 (A) and X (B and C).

**...**

*hg*gene (

*a*

_{1}) and QTL (

*a*

_{2}and

*d*

_{2}) as well as their epistatic interactions (

*I*and

*J*) for the QTL, detected by our joint model, on chromosomes 2 (A) and X (B and C).

**The MLEs of the QTL position, QTL effects described by growth parameters**

_{k(j)}=(

*a*

_{k(j)},

*b*

_{k(j)},

*c*

_{k(j)})

**, residual variance (σ**

_{j}), and correlation (ρ_{j}) in two different subpopulations of the F_{2}mouse population**...**

**The LR values and the corresponding**

*P*-values (in parentheses, estimated from simulation studies) for testing the additive effect of the*hg*locus (*a*_{1}), the additive (*a*_{2}) and dominant (*d*_{2}) effects of QTL, and the additive × additive (*I*) and additive**...**

We further tested the QTL effects and how they interact with the *hg* locus to affect growth trajectories. On the basis of the hypothesis test given in Equation 7 and others, we calculated the LR values for the additive and dominant effects of the QTL and its interaction effects with *hg* for all three QTL (Table 3). The QTL detected on chromosome 2 has highly significant additive and dominant effects on growth trajectories, operating in a dominant gene action manner as shown by small differences between genotypes *Qq* and *QQ* in both subpopulations (see Figure 3). This QTL also displays significant additive × additive and additive × dominant epistatic effects with the *hg* locus.

Located on the same chromosome, the two QTL detected on chromosome X exhibit different modes of gene action for growth. The first QTL at 3 cM from the first marker has a nonsignificant additive effect but highly significant dominant effect (Table 3; Figure 3B). When interacting with the *hg* gene, however, this dominant QTL displays an inverse pattern, *i.e.*, with a significant additive × additive but nonsignificant additive × dominant epistatic effects (Table 3). The second QTL at 37 cM from the first marker seems to act in a partial dominant manner (Figure 3C), with both types of epistatic effects being significant (Table 3). Except for the first QTL on chromosome X with a nonsignificant additive effect, the favorable allele at the other QTL that contribute to greater growth originates from the HG parent.

Because only two *hg* genotypes are included, we cannot estimate all the QTL-*hg* epistatic effects. The dynamic changes of different types of genetic effects for the *hg* and QTL across ages that can be estimated are

for the additive genetic effect of the *hg* locus,

for the additive genetic effect of the QTL,

for the dominant genetic effect of the QTL,

for the additive × additive genetic effect, and

for the additive × dominant genetic effect between *hg* and QTL. All these age-dependent changes of genetic effects are illustrated in Figure 4. The additive effect (*a*_{1}) of the *hg* locus increases rapidly with age, and so do the additive (*a*_{2}) and/or dominant effects (*d*_{2}) of the QTL, but with a lesser extent. The interaction effects (*I* and *J*) between the QTL and *hg* are quite stable over age, contributing to a significant part of the genetic variation throughout growth ontogeny.

## DISCUSSION

Traditional quantitative genetic theory proposes that genetic variation in a quantitative trait is due to polygenes each with a small effect on the phenotype and being sensitive to the environment (Lynch and Walsh 1998). Although this theory has led to substantial successes in the explanation of quantitative variation, it has been challenged by recent discoveries of QTL based on polymorphic markers. According to these QTL mapping results, a quantitative trait may be governed by unequally sized loci with a few having larger effects than many others (Mackay 2001). A 30–50% increase of body size in mice caused by the *hg* mutation (Bradford and Famula 1984) provides excellent evidence for the inclusion of a major gene in the genetic control of a quantitative trait.

As part of the complex network of genetic control, the expression of the *hg* locus should not be independent of the genetic background (Corva *et al.* 2001). It thus is of great interest to identify individual QTL that interact with the *hg* locus using mapping approaches. The identification of such QTL can improve our understanding of the interactions between pathways of signal transduction involved in the regulation of growth. This information can then be transferred to the development of techniques targeted to manipulate these growth-regulating pathways in mammals.

In this article, we have presented a statistical model for detecting interacting QTL involved in the regulation of growth through the *hg* locus. This model is the extension of our functional mapping approach (Ma *et al.* 2002; Wu *et al.* 2004a; Zhao *et al.* 2004) proposed to shed light on the genetic architecture of growth by incorporating its underlying developmental principles (von Bertalanffy 1957; Rice 1997; West *et al.* 2001) and the statistical methods for growth analysis (Diggle *et al.* 2002). A QTL is thought to be epistatic with the *hg* gene if its expression depends on the genetic background containing segregating *hg*. The extended model has power to estimate the differences in the gene action of a QTL expressed in different *hg* genotypes. Corva *et al.* (2001) constructed a segregating F_{2} population using a congenic *hg*/*hg* line and a wild-type inbred line. Molecular markers at genomic regions that may contain QTL for growth rate and body size were genotyped to construct a common linkage map for two F_{2} subpopulations, *hg*/*hg* and +/+. Thus, by estimating and testing the genetic effects of a QTL in these two different subpopulations, we can determine how the QTL, as a modifier, influences the expression of the *hg*/*hg* gene.

Our model has successfully detected three QTL that interact with the *hg* gene to govern the shape of growth trajectories. These detected QTL on chromosomes 2 and X affect growth curves with different modes of gene action. The estimation for the location of the QTL on chromosome 2 is broadly in agreement with that by previous QTL mapping based on a single-trait analysis (Corva *et al.* 2001), although our analysis is more informative in terms of age-dependent changes of QTL effects and the detection of epistasis in the genetic control of growth traits. The epistasis between the detected QTL and the *hg* locus is relatively small, relative to their main effects, but is thought to play a significant role in shaping growth processes. As illustrated by Figure 4, there are different patterns for the change of different genetic effects across ages. The additive effect of the *hg* locus increases rapidly with age, and so do the additive and/or dominant effects of the QTL, but to a lesser extent. The interaction effects between the QTL and *hg* are quite stable over age, contributing a significant part of the genetic variation throughout growth ontogeny.

The genetic control of body size across age has been observed in mice by both quantitative genetic (Cheverud 1984; Atchley and Zhu 1997) and QTL mapping approaches (Cheverud *et al.* 1996; Vaughn *et al.* 1999). It is suggested that the formation of such age-specific patterns is regulated by different genetic mechanisms. Falconer *et al.* (1978) speculated two general physiological mechanisms that determine the increase in body size in mice, but these mechanisms appear to act at different life stages (Atchley and Zhu 1997). This has been confirmed by QTL mapping of mouse growth traits in that early and late growth in mice were affected by distinct QTL, mapping to separate chromosome locations (Cheverud *et al.* 1996; Vaughn *et al.* 1999). In other animals, Carlborg *et al.* (2003) found that epistasis is important for early growth when the foundation for rapid growth is set by the development of internal organs, but less important for later growth involving the main deposition of body tissues. Our model has the capacity to quantify the patterns of the age-dependent change of genetic effects and, thus, to gain more insights into the interplay between gene action and development in developmental biological research.

In this study, we have reported only on the additive effect of the *hg* gene as well as its additive-related epistatic effects with other QTL detected by molecular markers. An F_{2} subpopulation heterozygous for the mutant and wild-type alleles that would allow estimation of effects due to dominance was not available. Using the available material, we have found three QTL on chromosomes 2 and X that interact with the *hg* locus to affect the shapes of the growth process. These genetic interactions are thought to play an important role in mediating the expression of the *hg* gene. Our model is fit by one modifier QTL, but it can be readily extended to include more modifiers that interact with each other and with the *hg* gene. The involvement of more QTL in the model can better reflect a practical situation in which there is a web of interacting genes in trait control (Segre *et al.* 2005). Although the available genetic data from Corva *et al.* (2001) were not subject to a multi-QTL analysis because of their low coverage of the mouse genome (including only chromosomes 1, 2, 4, 9, and X), our model derived in this article provides a powerful tool to shed light on the genetic architecture and regulation of growth rate and body size in mammals.

## Acknowledgments

We thank the two anonymous referees for their constructive comments on the article. This work is partially supported by National Institutes of Health grant DK52514 to J.M.C. and by an Outstanding Young Investigators award (no. 30128017) of the National Natural Science Foundation of China and the University of Florida Research Opportunity Fund (no. 02050259) to R.W. The publication of this article is approved as journal series R-09205 by the Florida Agricultural Experiment Station.

## References

- Atchley, W. R., and J. Zhu, 1997. Developmental quantitative genetics, conditional epigenetic variability and growth in mice. Genetics 147
**:**765–776. [PMC free article] [PubMed] - Bradford, G. E., and T. R. Famula, 1984. Evidence for a major gene for rapid postweaning growth in mice. Genet. Res. 44
**:**293–308. [PubMed] - Calvert, C. C., T. R. Famula, J. F. Bernier and G. E. Bradford, 1985. Serial composition during growth in mice with a major gene for rapid postweaning growth. Growth 49
**:**246–257. [PubMed] - Calvert, C. C., T. R. Famula, J. F. Bernier, N. Khaim and G. E. Bradford, 1986. Efficiency of growth in mice with a major gene for rapid postweaning gain. J. Anim. Sci. 62
**:**77–85. [PubMed] - Carlborg, O., S. Kerje, K. Schutz, L. Jacobsson, P. Jensen
*et al.*, 2003. A global search reveals epistatic interaction between QTL for early growth in the chicken. Genome Res. 13**:**413–421. [PMC free article] [PubMed] - Cheverud, J. M., 1984. Quantitative genetics and developmental constraints on evolution by selection. J. Theor. Biol. 110
**:**155–171. [PubMed] - Cheverud, J. M., E. J. Routman, F. A. M. Duarte, B. van Swinderen, K. Cothran
*et al.*, 1996. Quantitative trait loci for murine growth. Genetics 142**:**1305–1319. [PMC free article] [PubMed] - Churchill, G. A., and R. W. Doerge, 1994. Empirical threshold values for quantitative trait mapping. Genetics 138
**:**963–971. [PMC free article] [PubMed] - Corva, P. M., and J. F. Medrano, 2000. Diet effects on weight gain and body composition in high growth (hg/hg) mice. Physiol. Genomics 3
**:**17–23. [PubMed] - Corva, P. M., S. Horvat and J. F. Medrano, 2001. Quantitative trait loci affecting growth in
*highgrowth*(*hg*) mice. Mamm. Genome 12**:**284–290. [PubMed] - Dempster, A. P., N. M. Laird and D. B. Rubin, 1977. Maximum likelihood from incomplete data via EM algorithm. J. R. Stat. Soc. Ser. B 39
**:**1–38. - Diggle, P. J., P. Heagerty, K. Y. Liang and S. L. Zeger, 2002.
*Analysis of Longitudinal Data.*Oxford University Press, Oxford. - Falconer, D. S., I. Gauld and R. Roberts, 1978. Cell numbers and cell sizes in organs of mice selected for large and small body size. Genet. Res. 31
**:**387–401. [PubMed] - Horvat, S., and J. F. Medrano, 1995. Interval mapping of
*highgrowth*(*hg*), a major locus that increases weight gain in mice. Genetics 139**:**1737–1748. [PMC free article] [PubMed] - Horvat, S., and J. F. Medrano, 2001. Lack of
*Socs*2 expression causes the high-growth phenotype in mice. Genomics 72**:**209–212. [PubMed] - Hou, W., C. W. Garvan, W. Zhao, M. Behnke, F. D. Eyler
*et al.*, 2005. A generalized model for detecting genetic determinants underlying longitudinal traits with unequally spaced measurements and time-dependent correlated errors. Biostatistics 6**:**420–433. [PubMed] - Kirkpatrick, M., and N. Heckman, 1989. A quantitative genetic model for growth, shape, reaction norms, and other infinite-dimensional characters. J. Math. Biol. 27
**:**429–450. [PubMed] - Lander, E. S., and D. Botstein, 1989. Mapping Mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics 121
**:**185–199. [PMC free article] [PubMed] - Lynch, M., and B. Walsh, 1998.
*Genetics and Analysis of Quantitative Traits.*Sinauer, Sunderland, MA. - Ma, C.-X., G. Casella and R. L. Wu, 2002. Functional mapping of quantitative trait loci underlying the character process: a theoretical framework. Genetics 161
**:**1751–1762. [PMC free article] [PubMed] - Mackay, T. F. C., 2001. Quantitative trait loci in
*Drosophila.*Nat. Rev. Genet. 2**:**11–20. [PubMed] - Pletcher, S. D., and C. J. Geyer, 1999. The genetic analysis of age-dependent traits: modeling the character process. Genetics 153
**:**825–835. [PMC free article] [PubMed] - Pletcher, S. D., and F. Jaffrezic, 2002. Generalized character process models: estimating the genetic basis of traits that cannot be observed and that change with age or environmental conditions. Biometrics 58
**:**157–162. [PubMed] - Rice, S. H., 1997. The analysis of ontogenetic trajectories: when a change in size or shape is not heterochrony. Proc. Natl. Acad. Sci. USA 94
**:**907–912. [PMC free article] [PubMed] - Segre, D., A. Deluna, G. M. Church and R. Kishony, 2005. Modular epistasis in yeast metabolism. Nat. Genet. 37
**:**77–83. [PubMed] - Vaughn, T. T., L. S. Pletscher, A. Peripato, K. King-Ellison, E. Adams
*et al.*, 1999. Mapping quantitative trait loci for murine growth: a closer look at genetic architecture. Genet. Res. 74**:**313–322. [PubMed] - von Bertalanffy, L., 1957. Quantitative laws in metabolism and growth. Q. Rev. Biol. 32
**:**217–231. [PubMed] - West, G. B., J. H. Brown and B. J. Enquist, 2001. A general model for ontogenetic growth. Nature 413
**:**628–631. [PubMed] - Wong, M. L., A. Islas-Trejo and J. F. Medrano, 2002. Structural characterization of the mouse high growth deletion and discovery of a novel fusion transcript between suppressor of cytokine signaling-2 (
*Socs*-2) and viral encoded semaphorin receptor (*Plexin C*1). Gene 299**:**153–163. [PubMed] - Wu, R. L., C.-X. Ma, M. Chang, R. C. Littell, S. S. Wu
*et al.*, 2002. A logistic mixture model for characterizing genetic determinants causing differentiation in growth trajectories. Genet. Res. 19**:**235–245. [PubMed] - Wu, R. L., C.-X. Ma, M. Lin and G. Casella, 2004. a A general framework for analyzing the genetic architecture of developmental characteristics. Genetics 166
**:**1541–1551. [PMC free article] [PubMed] - Wu, R. L., C. X. Ma, M. Lin, Z. H. Wang and G. Casella, 2004. b Functional mapping of quantitative trait loci underlying growth trajectories using a transform-both-sides logistic model. Biometrics 60
**:**729–738. [PubMed] - Wu, R. L., Z. H. Wang, W. Zhao and J. M. Cheverud, 2004. c A mechanistic model for genetic machinery of ontogenetic growth. Genetics 168
**:**2383–2394. [PMC free article] [PubMed] - Zhao, W., C.-X. Ma, J. M. Cheverud and R. L. Wu, 2004. A unifying statistical model for QTL mapping of genotype-sex interaction for developmental trajectories. Physiol. Genomics 19
**:**218–227. [PubMed] - Zimmerman, D. L., and V. Nunez-Anton, 2001. Parametric modeling of growth curve data: an overview (with discussions). Test 10
**:**1–73.

**Genetics Society of America**

## Formats:

- Article |
- PubReader |
- ePub (beta) |
- PDF (340K)

- A non-stationary model for functional mapping of complex traits.[Bioinformatics. 2005]
*Zhao W, Chen YQ, Casella G, Cheverud JM, Wu R.**Bioinformatics. 2005 May 15; 21(10):2469-77. Epub 2005 Mar 15.* - Quantitative trait loci affecting growth in high growth (hg) mice.[Mamm Genome. 2001]
*Corva PM, Horvat S, Medrano JF.**Mamm Genome. 2001 Apr; 12(4):284-90.* - A unifying statistical model for QTL mapping of genotype x sex interaction for developmental trajectories.[Physiol Genomics. 2004]
*Zhao W, Ma C, Cheverud JM, Wu R.**Physiol Genomics. 2004 Oct 4; 19(2):218-27. Epub 2004 Aug 10.* - Mapping genetic loci that interact with myostatin to affect growth traits.[Heredity (Edinb). 2011]
*Cheng Y, Rachagani S, Dekkers JC, Mayes MS, Tait R, Reecy JM.**Heredity (Edinb). 2011 Dec; 107(6):565-73. Epub 2011 Jun 22.* - Using mouse models to dissect the genetics of obesity.[Trends Genet. 2002]
*Brockmann GA, Bevova MR.**Trends Genet. 2002 Jul; 18(7):367-76.*

- Genetic linkage map construction and QTL identification of juvenile growth traits in Torreya grandis[BMC Genetics. ]
*Zeng Y, Ye S, Yu W, Wu S, Hou W, Wu R, Dai W, Chang J.**BMC Genetics. 15(Suppl 1)S2* - A Maximum Likelihood Approach to Functional Mapping of Longitudinal Binary Traits[Statistical applications in genetics and mo...]
*Wang C, Li H, Wang Z, Wang Y, Wang N, Wang Z, Wu R.**Statistical applications in genetics and molecular biology. 11(6)10.1515/1544-6115.1675* - Genetic mapping of complex traits by minimizing integrated square errors[BMC Genetics. ]
*Wu S, Fu G, Chen Y, Wang Z, Wu R.**BMC Genetics. 1320* - A Dynamic Model for Functional Mapping of Biological Rhythms[Journal of biological dynamics. 2011]
*Fu G, Luo J, Berg A, Wang Z, Li J, Das K, Li R, Wu R.**Journal of biological dynamics. 2011 Jan; 5(1)84-101* - QTLMAS 2009: simulated dataset[BMC Proceedings. ]
*Coster A, Bastiaansen JW, Calus MP, Maliepaard C, Bink MC.**BMC Proceedings. 4(Suppl 1)S3*

- GeneGeneGene links
- GEO ProfilesGEO ProfilesRelated GEO records
- HomoloGeneHomoloGeneHomoloGene links
- MedGenMedGenRelated information in MedGen
- PubMedPubMedPubMed citations for these articles

- Functional Mapping of Quantitative Trait Loci That Interact With the hg Mutation...Functional Mapping of Quantitative Trait Loci That Interact With the hg Mutation to Regulate Growth Trajectories in MiceGenetics. Sep 2005; 171(1)239PMC

Your browsing activity is empty.

Activity recording is turned off.

See more...