Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region

被引:24
作者
DEsposito, M
Matarazzo, MR
Ciccodicola, A
Strazzullo, M
Matzarella, R
Quaderi, NA
Fujiwara, H
Ko, MSH
Rowe, LB
Ricco, A
Archidiacono, N
Rocchi, M
Schlessinger, D
DUrso, M
机构
[1] CNR,INT INST GENET & BIOPHYS,I-80125 NAPLES,ITALY
[2] WASHINGTON UNIV,SCH MED,DEPT MOL MICROBIOL,ST LOUIS,MO 63110
[3] DIBIT,TELETHON INST GENET & MED,I-20132 MILAN,ITALY
[4] WAYNE STATE UNIV,SCH MED,CTR MOL MED & GENET,DETROIT,MI 48202
[5] JACKSON LAB,BAR HARBOR,ME 04609
[6] UNIV BARI,IST GENET,I-70126 BARI,ITALY
关键词
D O I
10.1093/hmg/6.11.1917
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recently discovered second pseudoautosomal region (XqPAR) contains at least two genes, IL9R and SYBL1. Recent findings show that, like XpPAR genes, IL9R escapes X inactivation and its Y allele is also expressed, but SYBL1 seems to act like an X-linked gene, expressed from the active X chromosome but not from the inactive X or Y. Here we show that differences are also seen in the evolution of the sex chromosome locations of IL9R and SYBL1, IL9R is known to be autosomal in mice, and is X-linked only in primates. SYBL1, however, has been found to be on the X chromosome in all mammals tested, from marsupials to humans, Both genes were duplicated on the Y homologue of the terminal portion of the X chromosome during the evolution of Homo sapiens from other higher primates. The inactivation pattern of SYBL1 may be correlated with its longer history of X linkage, and at a more centromeric chromosomal position during evolution; the more recent X linkage and more telomeric position of the IL9R gene may explain its autosomal, 'uninactivated' transcriptional status.
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页码:1917 / 1923
页数:7
相关论文
共 31 条
[1]  
AFFARA NA, 1994, MOL GENETICS SEX DET, P225
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   TOWARD A PHYSICAL MAP OF THE XQ28 REGION IN MAN - LINKING COLOR-VISION, G6PD, AND COAGULATION FACTOR-VIII GENES TO AN X-Y HOMOLOGY REGION [J].
ARVEILER, B ;
VINCENT, A ;
MANDEL, JL .
GENOMICS, 1989, 4 (04) :460-471
[4]   EVOLUTION OF HOMOLOGOUS SEQUENCES ON THE HUMAN X-CHROMOSOME AND Y-CHROMOSOME, OUTSIDE OF THE MEIOTIC PAIRING SEGMENT [J].
BICKMORE, WA ;
COOKE, HJ .
NUCLEIC ACIDS RESEARCH, 1987, 15 (15) :6261-6271
[5]   STRUCTURE AND POLYMORPHISM OF HUMAN TELOMERE-ASSOCIATED DNA [J].
BROWN, WRA ;
MACKINNON, PJ ;
VILLASANTE, A ;
SPURR, N ;
BUCKLE, VJ ;
DOBSON, MJ .
CELL, 1990, 63 (01) :119-132
[6]   GENETIC HOMOLOGY AND CROSSING OVER IN THE X-CHROMOSOME AND Y-CHROMOSOME OF MAMMALS [J].
BURGOYNE, PS .
HUMAN GENETICS, 1982, 61 (02) :85-90
[7]   ON THE NATURE AND EXTENT OF XY PAIRING AT MEIOTIC PROPHASE IN MAN [J].
CHANDLEY, AC ;
GOETZ, P ;
HARGREAVE, TB ;
JOSEPH, AM ;
SPEED, RM .
CYTOGENETICS AND CELL GENETICS, 1984, 38 (04) :241-247
[8]   A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation [J].
DEsposito, M ;
Ciccodicola, A ;
Gianfrancesco, F ;
Esposito, T ;
Flagiello, L ;
Mazzarella, R ;
Schlessinger, D ;
DUrso, M .
NATURE GENETICS, 1996, 13 (02) :227-229
[9]   THE HUMAN PSEUDOAUTOSOMAL GM-CSF RECEPTOR ALPHA-SUBUNIT GENE IS AUTOSOMAL IN MOUSE [J].
DISTECHE, CM ;
BRANNAN, CI ;
LARSEN, A ;
ADLER, DA ;
SCHORDERET, DF ;
GEARING, D ;
COPELAND, NG ;
JENKINS, NA ;
PARK, LS .
NATURE GENETICS, 1992, 1 (05) :333-336
[10]   ESCAPE FROM X-INACTIVATION IN HUMAN AND MOUSE [J].
DISTECHE, CM .
TRENDS IN GENETICS, 1995, 11 (01) :17-22