Human Diallelic Insertion/Deletion Polymorphisms
AUTOR(ES)
Weber, James L.
FONTE
The American Society of Human Genetics
RESUMO
We report the identification and characterization of 2,000 human diallelic insertion/deletion polymorphisms (indels) distributed throughout the human genome. Candidate indels were identified by comparison of overlapping genomic or cDNA sequences. Average confirmation rate for indels with a ⩾2-nt allele-length difference was 58%, but the confirmation rate for indels with a 1-nt length difference was only 14%. The vast majority of the human diallelic indels were monomorphic in chimpanzees and gorillas. The ratio of deletion:insertion mutations was 4.1. Allele frequencies for the indels were measured in Europeans, Africans, Japanese, and Native Americans. New alleles were generally lower in frequency than old alleles. This tendency was most pronounced for the Africans, who are likely to be closest among the four groups to the original modern human population. Diallelic indels comprise ∼8% of all human polymorphisms. Their abundance and ease of analysis make them useful for many applications.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=378541Documentos Relacionados
- A rare insertion/deletion polymorphism at the HEXA locus
- Whole-genome experimental identification of insertion/deletion polymorphisms of interspersed repeats by a new general approach
- Direct Detection of Insertion/Deletion Polymorphisms in an Autosomal Region by Analyzing High-Density Markers in Individual Spermatozoa
- The mechanism of U insertion/deletion RNA editing in kinetoplastid mitochondria.
- Recognition of DNA insertion/deletion mismatches by an activity in Saccharomyces cerevisiae.