Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region

被引:21
作者
Schiebel, K
Meder, J
Rump, A
Rosenthal, A
Winkelmann, M
Fischer, C
Bonk, T
Humeny, A
Rappold, GA
机构
[1] Univ Heidelberg, Inst Human Genet, D-69120 Heidelberg, Germany
[2] Inst Mol Biotechnol, Dept Genome Anal, Jena, Germany
[3] Univ Erlangen Nurnberg, Inst Biochem, Erlangen, Germany
来源
CYTOGENETICS AND CELL GENETICS | 2000年 / 91卷 / 1-4期
关键词
D O I
10.1159/000056849
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolution, inheritance and recombination rate of genes located in the pseudoautosomal region 1 (PAR1) is exceptional within the human genome. Pseudoautosomal genes are identical on X and Y chromosomes and are not inherited in a sex linked manner. Due to an obligatory recombination event in male meiosis, pseudoautosomal genes are exchanged frequently between X and Y chromosomes. During the isolation, characterization and sequencing of a novel gene PPP2R3L, which was classified by sequence homology as a novel member of the protein phosphatase regulatory subunit families, it became apparent that cosmids of different origin harboring this gene are highly polymorphic between individuals, both at the nucleotide level and in the number and sequence of tandem repeats. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 45 条
[1]   MECHANISMS UNDERLYING TELOMERE REPEAT TURNOVER, REVEALED BY HYPERVARIABLE VARIANT REPEAT DISTRIBUTION PATTERNS IN THE HUMAN XP/YP TELOMERE [J].
BAIRD, DM ;
JEFFREYS, AJ ;
ROYLE, NJ .
EMBO JOURNAL, 1995, 14 (21) :5433-5443
[2]   High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: Implications for telomere biology and human evolution [J].
Baird, DM ;
Coleman, J ;
Rosser, ZH ;
Royle, NJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :235-250
[3]   Molecular mechanisms of the protein serine threonine phosphatases [J].
Barford, D .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (11) :407-412
[4]   Man to mouse - Lessons learned from the distal end of the human X chromosome [J].
Blaschke, RJ ;
Rappold, GA .
GENOME RESEARCH, 1997, 7 (12) :1114-1117
[5]   Characterization of single-nucleotide polymorphisms in coding regions of human genes [J].
Cargill, M ;
Altshuler, D ;
Ireland, J ;
Sklar, P ;
Ardlie, K ;
Patil, N ;
Lane, CR ;
Lim, EP ;
Kalyanaraman, N ;
Nemesh, J ;
Ziaugra, L ;
Friedland, L ;
Rolfe, A ;
Warrington, J ;
Lipshutz, R ;
Daley, GQ ;
Lander, ES .
NATURE GENETICS, 1999, 22 (03) :231-238
[6]  
CHARLESWORTH B, 1993, GENETICS, V134, P1289
[7]   Novel protein serine/threonine phosphatases: Variety is the spice of life [J].
Cohen, PTW .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (07) :245-251
[8]  
Cooper D, 1995, METABOLIC MOL BASES, P259
[9]   AN ESTIMATE OF UNIQUE DNA-SEQUENCE HETEROZYGOSITY IN THE HUMAN GENOME [J].
COOPER, DN ;
SMITH, BA ;
COOKE, HJ ;
NIEMANN, S ;
SCHMIDTKE, J .
HUMAN GENETICS, 1985, 69 (03) :201-205
[10]   PHOG, a candidate gene for involvement in the short stature of Turner syndrome [J].
Ellison, JW ;
Wardak, Z ;
Young, MF ;
Robey, PG ;
LaigWebster, M ;
Chiong, W .
HUMAN MOLECULAR GENETICS, 1997, 6 (08) :1341-1347