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PMID: 2793186 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Evolution of alpha-satellite DNA on human acrocentric chromosomes.

Genomics ·Vol. 5 ·No. 2 ·1989-08-00 ·Pages 332-44

Choo KH, Vissel B, Earle E

Abstract

In situ hybridization of five new and one previously described alpha-satellite sequences isolated from chromosome 21 libraries gave the following chromosomal distribution patterns: (a) two sequences (pTRA-1 and -4) hybridizing to chromosomes 13, 14, 15, 21, and 22 (also 19 and 20); (b) one sequence (pTRA-7) hybridizing to chromosome 14; and (c) three sequences (pTRA-2, -11 and -15) hybridizing to chromosomes 13, 14, and 21, with significant but weaker signals on 15 and 22. These results suggested the sharing of alphoid domains between different acrocentric chromosomes and the coexistence of multiple domains on each chromosome. Analysis of somatic cell hybrids carrying a single human acrocentric chromosome using pTRA-2 demonstrated a higher-order repeating structure common to chromosomes 13, 14, and 21, but not to 15 and 22, providing direct evidence for sequence homogenization in this domain among the former three chromosomes. We present a model of evolution and genetic exchange of alpha sequences on the acrocentric chromosomes which can satisfactorily explain these and previous observations of (a) two different alphoid subfamilies, one common to chromosomes 13 and 21 and the other common to chromosomes 14 and 22, (b) a different alphoid subfamily on chromosome 22, and (c) nonrandom participation of chromosomes 13 and 14, and 14 and 21 in Robertsonian translocations.

MeSH Terms
Blotting, Southern Centromere Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 22 Cloning, Molecular DNA, Satellite Humans Hybrid Cells Models, Genetic Nucleic Acid Hybridization Translocation, Genetic
Chemicals
DNA, Satellite
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Choo K H
Murdoch Institute for Research into Birth Defects, Royal Children's Hospital, Melbourne, Victoria, Australia.
Vissel B
Earle E
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1989-08-00
Pages
332-44
Language
English
Region
United States
NLM ID
8800135
Subset
IM
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