SEQUENCE DIVERSITY AND CHROMOSOMAL DISTRIBUTION OF YOUNG ALU REPEATS

被引:40
作者
ARCOT, SS
SHAIKH, TH
KIM, JY
BENNETT, L
ALEGRIAHARTMAN, M
NELSON, DO
DEININGER, PL
BATZER, MA
机构
[1] LAWRENCE LIVERMORE NATL LAB,CTR HUMAN GENOME,BIOL & BIOTECHNOL RES PROGRAM,LIVERMORE,CA 94551
[2] ALTON OCHSNER MED FDN & OCHSNER CLIN,MOLEC GENET LAB,NEW ORLEANS,LA 70121
[3] LOUISIANA STATE UNIV,MED CTR,DEPT BIOCHEM & MOLEC BIOL,NEW ORLEANS,LA 70112
关键词
REPETITIVE DNA; POLYMORPHISM HUMAN; SOMATIC CELL HYBRID; PRIMATE; MICROSATELLITE; DIRECT REPEATS; POLYMERASE CHAIN REACTION;
D O I
10.1016/0378-1119(95)00317-Y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Members of the recently inserted human-specific (HS)/predicted variant (PV) subfamily of Alu elements were sequenced. A number of these Alu elements share greater than 98% sequence identity with the subfamily consensus sequence, and they are flanked by perfect 5' and 3' direct repeats ranging in size from 6 to 15 nucleotides (nt). Based on the low number of random mutations, the estimated average age of these elements was calculated to be 1.5 million years (Myr). All the young Alu subfamily members were restricted to the human genome, as judged by polymerase chain reaction (PCR) amplification of human and non-human primate DNA samples using the unique flanking sequences specific for each Alu element. The chromosomal locations of several Alu elements belonging to the young subfamilies, designated as HS/PV and Sb2, were determined by PCR amplification of DNA samples from human/rodent somatic cell hybrid panels. A statistical analysis of the chromosomal distribution pattern showed that the recently inserted Alu elements appear to integrate randomly in the human genome.
引用
收藏
页码:273 / 278
页数:6
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