Annotation, nomenclature and evolution of four novel homeobox genes expressed in the human germ line

被引:37
作者
Booth, H. Anne F. [1 ]
Holland, Peter W. H. [1 ]
机构
[1] Univ Oxford, Dept Zool, Oxford OX1 3PS, England
基金
英国生物技术与生命科学研究理事会;
关键词
molecular evolution; human genome; gene family; otx; paired; embryonic stem cells;
D O I
10.1016/j.gene.2006.07.034
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The homeobox genes comprise a large gene superfamily characterised by a conserved DNA motif encoding the homeodomain. Most horneodomain proteins function as transcription factors, and many have important roles in embryonic development and cell differentiation. Here we describe, annotate and name four novel homeobox genes in the human genome: ARGFX, DPRX TPRX1 and DUXA. Each has generated multiple retrotransposed (processed) pseudogenes; these are reliable indicators of germ-line expression because only in germ-line cells can retrotransposition result in inheritance to the next generation. The retrotransposed sequences were exploited here as a novel means to deduce exon-intron boundaries. All four novel genes show accelerated rates of protein sequence evolution. This fast rate of sequence change may be connected with roles in human reproductive biology. Deducing the evolutionary origins of these genes is not straightforward, but we propose that TPRX1, DPRX and DUXA are highly divergent derivatives of the CRX gene, itself a member of the Otx homeobox gene family. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 36 条
[1]  
[Anonymous], 1989, Cladistics, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X
[2]   Active genes in junk DNA?: Characterization of DUX genes embedded within 3.3 kb repeated elements [J].
Beckers, MC ;
Gabriëls, J ;
van der Maarel, S ;
De Vriese, A ;
Frants, RR ;
Collen, D ;
Belayew, A .
GENE, 2001, 264 (01) :51-57
[3]   Homeobox genes and disease [J].
Boncinelli, E .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (03) :331-337
[4]   Eleven daughters of NANOG [J].
Booth, HAF ;
Holland, PWH .
GENOMICS, 2004, 84 (02) :229-238
[5]  
Brandenberger Ralph, 2004, BMC Developmental Biology, V4, P1
[6]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[7]  
Burglin T.R., 2005, Encyclopedia of molecular cell biology and molecular medicine, V6, P179
[8]   Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells [J].
Chambers, I ;
Colby, D ;
Robertson, M ;
Nichols, J ;
Lee, S ;
Tweedie, S ;
Smith, A .
CELL, 2003, 113 (05) :643-655
[9]   Human STELLAR, NANOG, and GDF3 genes are expressed in pluripotent cells and map to chromosome 12p13, a hotspot for teratocarcinoma [J].
Clark, AT ;
Rodriguez, RT ;
Bodnar, MS ;
Abeyta, MJ ;
Cedars, MI ;
Turek, PJ ;
Firpo, MT ;
Pera, RAR .
STEM CELLS, 2004, 22 (02) :169-179
[10]  
Clark LN, 1996, CHROMOSOMA, V105, P180, DOI 10.1007/BF02509499