| Literature DB >> 2841225 |
C Fowler1, R Drinkwater, J Skinner, L Burgoyne.
Abstract
Human satellite III DNA contains a complex polymorphism, which appears to be TaqI-specific. Its likely cause is a two-step point mutation in the pentameric repeat TTCCA, typical of satellite III. Hybridization of the satellite-III sequence-related probe that demonstrates this polymorphism is directly attributable to clusters of "pure" pentameric TTCCA repeats in the genome. The sites of such repeats include the 3.4-kb fragment specific to the Y chromosome and a limited number of autosomes. The polymorphism arises from the latter and is likely to include chromosomes containing so-called K domain satellite III sequences found, for example, in chromosomes 9 and 15. Segregation of the polymorphic fragments appears to follow orthodox genetics.Entities:
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Year: 1988 PMID: 2841225 DOI: 10.1007/BF00366249
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132