The UTX gene escapes X inactivation in mice and humans

被引:205
作者
Greenfield, A [1 ]
Carrel, L
Pennisi, D
Philippe, C
Quaderi, N
Siggers, P
Steiner, K
Tam, PPL
Monaco, AP
Willard, HF
Koopman, P
机构
[1] Univ Queensland, Ctr Cellular & Mol Biol, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Dept Anat Sci, Brisbane, Qld 4072, Australia
[3] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[4] Case Western Reserve Univ, Sch Med, Dept Genet, Ctr Human Genet, Cleveland, OH 44106 USA
[5] Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[6] St Marys Hosp, Sch Med, Dept Biochem & Mol Genet, London W2 1PG, England
[7] Childrens Med Res Inst, Embryol Unit, Wentworthville, NSW 2145, Australia
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1093/hmg/7.4.737
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
We recently have identified a ubiquitously transcribed mouse Y chromosome gene, Uty, which encodes a tetratricopeptide repeat (TPR) protein, A peptide derived from the UTY protein confers H-Y antigenicity on male cells, Here we report the characterization of a widely transcribed X-linked homologue of Uty,called Utx, which maps to the proximal region of the mouse X chromosome and which detects a human X-linked homologue at Xp11.2, Given that Uty is ubiquitously transcribed, we assayed for Utx expression from the inactive X chromosome (Xi) in mice and found that Utx escapes X chromosome inactivation, Only Smcx and the pseudoautosomal Sts gene on the mouse X chromosome have been reported previously to escape inactivation. The human UTX gene was also found to be expressed from Xi. We discuss the significance of these data for our understanding of dosage compensation of X-Y homologous genes in humans and mice.
引用
收藏
页码:737 / 742
页数:6
相关论文
共 37 条
[1]   A NOVEL X-GENE WITH A WIDELY TRANSCRIBED Y-LINKED HOMOLOG ESCAPES X-INACTIVATION IN MOUSE AND HUMAN [J].
AGULNIK, AI ;
MITCHELL, MJ ;
MATTEI, MG ;
BORSANI, G ;
AVNER, PA ;
LERNER, JL ;
BISHOP, CE .
HUMAN MOLECULAR GENETICS, 1994, 3 (06) :879-884
[2]  
[Anonymous], [No title captured]
[3]   X-CHROMOSOME INACTIVATION MAY EXPLAIN THE DIFFERENCE IN VIABILITY OF XO HUMANS AND MICE [J].
ASHWORTH, A ;
RASTAN, S ;
LOVELLBADGE, R ;
KAY, G .
NATURE, 1991, 351 (6325) :406-408
[4]   VIABILITY, DEVELOPMENT AND INCIDENCE OF CHROMOSOME-ANOMALIES OF PREIMPLANTATION EMBRYOS FROM XO MICE [J].
BANZAI, M ;
OMOE, K ;
ISHIKAWA, H ;
ENDO, A .
CYTOGENETICS AND CELL GENETICS, 1995, 70 (3-4) :273-277
[5]   Mouse X Chromosome [J].
Boyd, Y ;
Herman, GE ;
Avner, P ;
Disteche, CM ;
Adler, D ;
Reed, V ;
Blair, HJ .
MAMMALIAN GENOME, 1997, 7 (Suppl 1) :S313-S326
[6]   Expression of genes from the human active and inactive X chromosomes [J].
Brown, CJ ;
Carrel, L ;
Willard, HF .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 60 (06) :1333-1343
[7]  
BURGOYNE PS, 1985, J REPROD FERTIL, V75, P633, DOI 10.1530/jrf.0.0750633
[8]   Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene [J].
Carrel, L ;
Hunt, PA ;
Willard, HF .
HUMAN MOLECULAR GENETICS, 1996, 5 (09) :1361-1366
[9]   X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse [J].
Carrel, L ;
Clemson, CM ;
Dunn, JM ;
Miller, AP ;
Hunt, PA ;
Lawrence, JB ;
Willard, HF .
HUMAN MOLECULAR GENETICS, 1996, 5 (03) :391-401
[10]   MOLECULAR AND GENETIC-MAPPING OF THE MOUSE MDX LOCUS [J].
CAVANNA, JS ;
COULTON, G ;
MORGAN, JE ;
BROCKDORFF, N ;
FORREST, SM ;
DAVIES, KE ;
BROWN, SDM .
GENOMICS, 1988, 3 (04) :337-341