Ruault Myriam, Ventura Mario, Galtier Nicolas, Brun Marie-Elisabeth, Archidiacono Nicoletta, Roizès Gérard, De Sario Albertina
Institut de Génétique Humaine, CNRS UPR 1142, 141, Rue de la Cardonille, 34396 Montpellier, France.
Genomics. 2003 Apr;81(4):391-9. doi: 10.1016/s0888-7543(03)00025-9.
In this paper, we show that the BAGE (B melanoma antigen) gene family was generated by chromosome rearrangements that occurred during the evolution of hominoids. An 84-kb DNA fragment derived from the phylogenetic 7q36 region was duplicated in the juxtacentromeric region of either chromosome 13 or chromosome 21. The duplicated region contained a fragment of the MLL3 gene, which, after juxtacentromeric reshuffling, generated the ancestral BAGE gene. Then, this ancestral gene gave rise to several independent genes through successive rounds of inter- and intrachromosome duplications. Comparison of synonymous and nonsynonymous mutations in putative coding regions shows that BAGE genes, but not the BAGE gene fragments, are under selective pressure. Our data strongly suggest that BAGE proteins have a function and that juxtacentromeric regions, whose plasticity is now largely proved, are not a simple junkyard of gene fragments, but may be the birth site of novel genes.
在本文中,我们表明BAGE(B黑色素瘤抗原)基因家族是由类人猿进化过程中发生的染色体重排产生的。一个源自系统发育7q36区域的84kb DNA片段在13号或21号染色体的近着丝粒区域发生了复制。复制区域包含MLL3基因的一个片段,该片段在近着丝粒重排后产生了祖先BAGE基因。然后,这个祖先基因通过连续几轮的染色体间和染色体内复制产生了几个独立的基因。对推定编码区域中同义突变和非同义突变的比较表明,BAGE基因而非BAGE基因片段受到选择压力。我们的数据有力地表明,BAGE蛋白具有功能,并且近着丝粒区域(其可塑性现已得到充分证明)并非简单的基因片段垃圾场,而是可能成为新基因的诞生地。