U.S. flag

An official website of the United States government

PMC Full-Text Search Results

Items: 3

1.
Fig. 2.

Fig. 2. From: Human endogenous retrovirus K solo-LTR formation and insertional polymorphisms: Implications for human and viral evolution.

Detection of HERV-K solo LTRs. Two primer sets were used for each polymorphic HERV-K locus identified in the unblotting analysis, labeled A and B. A similar PCR strategy was used to probe for polymorphisms at the nine other known human-specific HERV-K loci (data not shown), and only HERVK1p31 was found to be polymorphic. Primer set A was used to amplify the 5′ LTR of the full-length element, and primer set B was used to amplify the corresponding solo LTR or unoccupied preintegration site at each locus. Samples 1–10 are the same as in , and the remaining samples are labeled according to the population of origin of their donors. The primer set used in each reaction is indicated to the left of the unblots, and the identity of each product, confirmed by sequence analysis, is indicated the right of the unblots.

Jennifer F. Hughes, et al. Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1668-1672.
2.
Fig. 3.

Fig. 3. From: Human endogenous retrovirus K solo-LTR formation and insertional polymorphisms: Implications for human and viral evolution.

Multiple alleles of HERV-K11q22 and its solo LTRs. The 5′ and 3′ LTRs of the full-length element and the solo LTR contain six polymorphic sites in the 968 base pairs sequenced in the five heterozygous individuals studied. The base pair positions and the identities of these sites are indicated. The ancestral states were determined from character state reconstructions (304, 824, and 928) or assigned by homology to other, closely related HERV-K loci (32, 345, and 575), in cases of ambiguity. There are two alleles (A and B) of the full-length element and three alleles (1, 2, and 3) of the solo LTR. The polymorphic sites that differ from the inferred ancestral sequence are shown in boxes. Of the five heterozygous individuals, two had full-length element A and solo-LTR 2. The remaining individuals each had one of the following combinations: A and solo-LTR 1, B and solo-LTR 1, and B and solo-LTR 3.

Jennifer F. Hughes, et al. Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1668-1672.
3.
Fig. 1.

Fig. 1. From: Human endogenous retrovirus K solo-LTR formation and insertional polymorphisms: Implications for human and viral evolution.

Detection of HERV-K polymorphisms. (Upper) The position of the K10 oligonucleotide probe and putative Ase I sites relative to a typical HERV-K element. (Lower) Unblotting of a set of human genomic DNA samples digested with Ase I and probed with K10. Gray arrows indicate bands that are polymorphic within the sample. Bands predicted from the genomic database are plotted to the left of the blot, and the bands that appear to be polymorphic are indicated. Five of these elements have been identified: HERV-K108, 109, and 115 (, ); and HERV-K11q22 and 12q14 (). The HERV-K element 3q24 is not full-length and was identified in the clone with GenBank accession no. AC069410 (Human Bacterial Artificial Chromosome Library, Roswell Park Cancer Institute, Buffalo, NY). The band marked 108b is the size expected for the central LTR of the tandem form of HERV-K 108 () (see ).

Jennifer F. Hughes, et al. Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1668-1672.

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center