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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Nat Genet. Author manuscript; available in PMC May 16, 2006.
Published in final edited form as:
Published online Aug 7, 2005. doi:  10.1038/ng1618
PMCID: PMC1462868
NIHMSID: NIHMS4988

Intragenic tandem repeats generate functional variability

Abstract

Tandemly repeated DNA sequences are highly dynamic components of genomes1. Most repeats are in intergenic regions, but some are found within coding sequences or pseudogenes2. In humans, expansion of intragenic triplet repeats is associated with various diseases, including Huntington’s chorea and fragile X syndrome3,4. The persistence of intragenic repeats in genomes argues in favor of a compensating benefit. Here we show that in the Saccharomyces genome, the majority of the genes containing intragenic repeats encode cell wall proteins. The repeats trigger frequent recombination events within the gene or between the gene and a pseudogene, causing expansion and contraction in the gene size. This size variation creates quantitative alterations in phenotypes (e.g. adhesion, flocculation, biofilm formation). We propose that variation in intragenic repeat number provides the functional diversity of cell surface antigens that, in fungi and other pathogens, allows rapid adaptation to the environment and/or elusion of the host immune system.

The sequenced and annotated genome of Saccharomyces cerevisiae provides a unique opportunity to determine the function of intragenic repeat sequences. To identify the S. cerevisiae open reading frames (ORFs) that contain intragenic tandem repeats, we scanned all 6591 open reading frames for the presence of long (>40 nt) or short (3-39 nt) repeats (see Methods for details). The search yielded 44 ORFs: 29 ORFs with repeats longer than 40 nt (Fig. 1a) and 15 ORFs with small repeats (Fig. 1b). These 44 genes showed unexpected functional similarities. Eighteen of the 29 ORFs (62 %) with conserved long repeats encode cell wall proteins. By comparison, only 1.3 % of all S. cerevisiae open reading frames are cell surface proteins (88 out of 6591). An additional 4 genes (CTR1, MNN4, MSB2, HKR1) are plasma membrane proteins with extracellular domains. Hence, more than 75% (22/29) of all genes with long intragenic tandem repeats encode cell-surface proteins. The group of 15 genes with short repeats contains only one cell wall gene (SCW11). However, several genes in this group encode regulators of cell wall synthesis and maintenance, such as MSS11 (regulator of adhesion), WSC3 (regulator of cell wall integrity) and CHS5 (regulator of chitin biosynthesis).

Fig. 1
S. cerevisiae genes containing conserved intragenic repeats

Remarkably, all repeats were found to be in-frame, so that deletion or addition of repeat units would not alter the reading frame. In order to verify that the intragenic repeat regions show size variations between yeast strains due to expansion or contraction of the repeats, we amplified each of the identified repetitive regions by PCR and compared the sizes for six different S. cerevisiae strains. The length of the repeat region in 35 of the 44 genes with intragenic repeats varies from strain to strain (Fig. 2 and Supplementary Fig. 1, 2 online). Virtually all cell surface genes with conserved repeats showed size variation. Moreover, strains that have a ploidy greater than haploid often harbor several different alleles of the same gene. The size difference between the genes in different S. cerevisiae strains is remarkable, as the size of most genes has been conserved over millions of years in different yeast species5. To confirm that genes in these six strains do not generally vary in size, we analyzed 16 genes without repeats: 8 cell surface genes, 4 long genes (> 3kb) and 4 genes encoding various enzymes. None of these 16 genes lacking repeats show any length differences among the six S. cerevisiae strains (Supplementary Fig. 3 online).

Fig. 2
Intragenic repetitive domains vary in size

To characterize the events leading to expansion and contraction of intragenic repeats, we designed a system that permitted us to detect events occurring within the repeat region in one of the genes with repeats (FLO1). FLO1 is a homologue of the human mucin genes and encodes a cell surface adhesin, a mannoprotein responsible for adherence to other yeast cells (flocculation) as well as certain surfaces2,6. A single copy of the URA3 gene was inserted among the repeats of the genomic copy of FLO1 in the S288C strain (Fig 3a). In this strain, the FLO1 gene is 4.6 kb long and contains 18 repeats of about 100 nt, separated by a less conserved 45-nt sequence. The FLO1::URA3 strains were grown on medium without uracil and then spread on plates containing 5 fluoro-orotic acid (5-FOA), which selects for mitotic segregants that have lost the URA3 marker (Fig. 3b).

Fig 3
Intragenic repeats are hot-spots for recombination

The FLO1::URA3 strains give rise to Ura segregants at a high frequency (≈ 1 × 10−5; Fig. 3b,c). Moreover, the frequency of segregants gradually increases with increasing numbers of repeated DNA motifs surrounding the URA3 marker (Fig. 3c). The Ura segregants have alterations in the number of repeats as compared with the starting strain. Most of the new FLO1 alleles obtained after loss of the URA3 marker have fewer repeat units than the wild-type FLO1 allele. However, about 15 percent (7/50) of the alleles gained extra repeats, causing increases in the gene size of up to 1 kb. This remarkable result indicates that the URA3 marker is not just “looped out” by unequal crossover between repeat units surrounding the marker (see further). Moreover, the wide range of different alleles generated in this procedure indicates that different repeat units can freely recombine with each other. Sequence analysis of the wild-type FLO1 allele and three of the novel short FLO1 alleles confirmed that each of these short alleles had lost several repeat units. Moreover, since all different repeats in the FLO genes show slight sequence differences2, it is possible to determine which repeat units were lost by aligning the sequences of the new alleles to that of the wild-type FLO1 sequence (Supplementary Fig. 4 online). This analysis shows that, in all cases, an upstream repeat unit had fused with one of the downstream units, thereby removing several repeat units in between while preserving the open reading frame.

Both the PIR and the FLO gene families have pseudogenes containing repeats that are similar to those in the functional copies2,7. These pseudogenes may provide additional genetic information that could be incorporated by a recombination event. In fact, two independent strains contain a novel FLO1 allele formed by the fusion of the first repeat unit of FLO1 with a repeat unit similar to those in FLO1 found in the FLO1 pseudogene YAR062W. This pseudogene is located approximately 12 kb downstream from the FLO1 termination codon2 (Fig. 4a). Sequence analysis of the FLO1-YAR062W fusion shows that the first FLO1 repeat had recombined with the repeat in the pseudogene, thereby looping out the complete 12 kb between the repeats in FLO1 and the pseudogene. Southern blotting and CHEF chromosome analysis confirmed the loss of about 12 kb between FLO1 and the pseudogene on chromosome I (Fig. 4b,c).

Fig 4
Repeats in pseudogenes provide an additional source of variability

To determine the functional consequence of continued variation of cell wall genes carrying intragenic repeats, we compared eight newly generated FLO1 alleles (2.9 kb to 5.4 kb, Fig. 5a,b) for their effects on various adhesion phenotypes associated with the FLO1 gene6. Each FLO1 size variant was fused to the inducible GAL1 promoter in the S288C background. In S288C, all 5 FLO genes are transcriptionally silent2,8, so the ectopic expression of these GAL1P-FLO1 constructs permits evaluation of the contribution of the particular FLO1 allele. As expected, none of the strains displayed any adhesion phenotypes on glucose medium. However, when these strains carrying the GAL1P-FLO1 fusion were grown on galactose medium (YPGal), there was a striking, linear correlation between gene size and the extent of adhesion: as the FLO1 proteins become longer (carrying more repeats), the adhesion properties gradually become stronger (Fig. 5c,d). Flocculation (i.e. adhesion to other yeast cells) shows the same quantitative relationship to the repeat number: the more repeats, the greater the fraction of flocculating cells (Fig. 5e). The observed correlation between the number of repeats and gain-of-function of Flo1 relies on the specific amino acids encoded by the repeats because insertion of URA3 in the FLO1 repeat region totally abolished adhesion (not shown).

Fig. 5
Instability of the FLO1 repeats generates functional variability

To analyze the mechanism involved in the recombination of intragenic FLO1 repeats, the stability of the repeats in various key DNA repair and recombination mutants was measured (Table 1). Elegant studies on recombination of intergenic repeats have shown that in most cases, replication slippage and/or the repair of doubled-stranded breaks during DNA replication are the main mechanisms for repeat expansion and contraction913. These studies also identified various RAD genes that influence mutation frequencies in repeats. We found that loss of the RAD27-encoded flap endonuclease, which causes the formation of double-stranded breaks during replication12-15, increases the instability of FLO1 repeats almost 40-fold. The increased recombination frequency in rad27Δ mutants suggests that FLO1 repeat instability is associated with the occurrence of double-stranded breaks due to defective DNA replication12,14,15. Deletion of RAD52 and RAD50 severely reduces the frequency of rearrangements, whereas deletion of the RecA homologue RAD51 does not affect the frequency. Rad51 is required for ATP-dependent strand invasion during conservative DNA repair and recombination processes16. The absence of an effect in rad51Δ mutants suggests that FLO1 recombination does not require strand invasion and thus gene conversion, break-induced replication and crossing over are unlikely recombination mechanisms. Instead, the decrease in recombination observed in rad50Δ, rad52Δ and rad1Δ rad52Δ mutants suggests that the process depends on break repair by single-strand annealing11, a conclusion further supported by the decrease in FLO1 recombination in the rad59Δ mutant, which is known to be deficient in this type of DNA repair17. Moreover, in contrast to many other possible models, the proposed model also accounts for the expansion in the number of repeats found in some of the Ura segregants. Taken together, the recombination frequencies observed in the various mutants indicate that recombination between the FLO1 repeats is caused by a replication slippage process similar to that observed in intergenic repeats (Supplementary Fig. 5 online).

Table 1
Frequency of recombination between intragenic repeats in selected DNA repair and recombination mutants

Our data show that expansion and contraction of repeats results in gradual, quantitative and fully reversible functional changes that permit existing features of the organism to be rapidly attuned to a particular environment. The presence of repeats in the FLO adhesins, for example, enables Saccharomyces to adapt its adhesion behavior, finding an optimal balance between adherent cells and free cells that can escape from the mass and explore new surfaces. For pathogenic fungi like Candida albicans and Candida glabrata, such recombination events in their adhesin genes (ALS and EPA genes, respective homologs of FLO1) could enable the cells to adhere to novel host tissues. Variability at the cell surface of these pathogens may also permit evasion of the host immune system2. Interestingly, intragenic repeats are also present in cell-surface genes of non-fungal pathogens, including Haemophilus influenzae18, Bacillus anthracis19, Leishmania infantum20, and various Plasmodium species21. Hence, recombination of intragenic repeats may be a widespread mechanism among microorganisms to generate cell surface diversity from a single gene. This mechanism differs from that in Trypanosomes, where diversity arises from the expression of different, unlinked members of a large library of genes22.

In multicellular eukaryotes, repeat expansion and contraction may have significance for the generation of variability in genes other than those that function in the cell surface. For example, the rapid yet topologically conservative evolution of canine skeletal morphology has been attributed to the expansion and contraction of intragenic repeats within developmental genes23. In humans, the mucin (MUC) genes, which are homologues of the S. cerevisiae FLO genes, contain variable numbers of a 60 bp intragenic tandem repeat. Elevated expression of MUC genes induces tumorigenesis24 and is currently used as a marker for malignant tumors. Extensive size differences in MUC genes have been reported25, but the relationship of this variation to malignancy is not yet known.

METHODS

Bioinformatics

To find intragenic repeats, the EMBOSS ETANDEM software26 was used to screen the sequences of all S. cerevisiae ORFs. Two separate screens identified the short (3-39 nt) or long (>40 nt) repeats. ETANDEM threshold score was set at 20. This first screen identified 323 ORFs with long repeats and 859 ORFs with short repeats (see Supplementary Table 1 online). A secondary screen further refined the results of these two initial screens by excluding dubious ORFs and ORFs with poorly conserved (degenerated) repeats. Intragenic repeats were considered significant if three conditions were fulfilled: (1) the ORF was not a dubious or hypothetical ORF according to the Saccharomyces genome database (http://www.yeastgenome.org/); (2) repeat conservation was at least 85% and (3) the number of repeats was at least 20 for trinucleotide repeats, 16 copies for repeats between 4 and 10 nucleotides, 10 for repeats with a length between 11 and 39 nucleotides and 3 copies for repeats of at least 40 nucleotides.

Strains and Molecular Biology

All yeast strains used are listed in Supplementary Table 2 online. Yeast cultures were grown as described before27. YPGal medium contained 2% raffinose, 2% galactose (Sigma Chemical Co.), 2% peptone (Difco) and 1% yeast extract (Difco). Standard procedures and reagents for molecular biology were used. The URA3 marker was inserted into the intragenic repeats in FLO1 by transformation. A URA3 cassette was PCR amplified using primers containing 5′ tails with sequence homologous to the consensus repeated motif found in FLO1 and the plasmid pRS30628 as a template; these constructs were transformed into a Ura recipient. Due to the similarity between the repeats, the construct integrated at various positions in the FLO1 repeats, thereby replacing a variable number of repeats. In some cases, insertion of URA3 led to an increase in repeat units. Real-time PCR using the ABI 7500 system (Applied Biosystems) was carried out with the appropriate enzymes and chemicals from Applied Biosystems as recommended by the supplier. All PCR primers are listed in Supplementary Table 3 online. CHEF chromosome separation was performed using a BioRad CHEF-DRII using the protocol supplied by BioRad. Flocculation and adhesion to polystyrene were tested as described previously6,29.

Recombination analysis

In order to measure the recombination frequency in the various FLO1::URA3 strains, single colonies growing on SD −Ura plates were inoculated in SD −Ura medium, and used to inoculate a 50 ml culture with an initial cell concentration of 1× 106 cells ml−1. This culture was shaken for 14 h at 28 °C, after which cells were harvested, washed with sterile distilled water and resuspended in water to a concentration of 5× 108 cells ml−1. This cell suspension was used to make a dilution series of which 150 microliter was plated onto SD plates containing 1 g l−1 5-fluoroorotic acid (5-FOA) to select for Ura segregants. Since there is no growth on non-selective medium, frequencies measured by this method provide a good estimate of actual recombination rates (number of events per cell division). Loss of the URA3 marker was confirmed by PCR. All experiments were repeated at least 3 times and the average number of colonies was used to calculate the recombination frequency. Statistical significance was estimated using the student t-test.

Acknowledgments

The authors thank Anthony Sinskey, Angelica Amon and all Fink lab members for the valuable discussions, Kimberly Walker for assistance with the bioinformatics and Tom DiCesare for help with the graphics. K.J.V. is a post-doctoral fellow of the Fund for Scientific Research Flanders (F.W.O. Vlaanderen) and a D. Collen Fellow of the Belgian American Educational Foundation (B.A.E.F.). G.R.F. is an American Cancer Society Professor of Genetics. This research was supported by NIH grant 5RO1 GM35010 to G.R.F.

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