Iwase Mineyo, Kaneko Satoko, Kim Hielim, Satta Yoko, Takahata Naoyuki
Department of Biosystems Science, Graduate University for Advanced Studies, Hayama, Japan.
Cells Tissues Organs. 2007;186(1):49-59. doi: 10.1159/000102680.
Amelogenin (AMEL) arose prior to the emergence of tetrapods and transposed into an intron of the Rho GTPase-activating protein 6 gene. In the mammalian lineage leading to eutherians, a pair of homologous autosomes with this nested gene structure fused with the then already differentiating sex chromosomes by suppressing homologous recombination. As sex-chromosomal differentiation extended to the fused region, a pair of homologous AMEL genes too differentiated from each other in two steps; first in the 5' region (the promoter region to transposon MER5 in intron 2) and second in the remaining 3' region. This resulted in gametologous AMELX and AMELY in the eutherian sex chromosomes. Although the early differentiation of the 5' region between AMELX and AMELY is consistent with the lowered expression level of AMELY, there is no indication for deterioration of AMELY at the amino acid level. Rather, both AMELX and AMELY in particular lineages might undergo positive selection, followed by negative selection to preserve established function. Based on patterns and levels of AMELX and AMELY polymorphisms in the human population, it is also argued that a recombination cold spot near AMELX might be related to the cause of the ancient pseudoautosomal boundary.
釉原蛋白(AMEL)在四足动物出现之前就已产生,并转座到Rho GTP酶激活蛋白6基因的一个内含子中。在通向真兽类的哺乳动物谱系中,一对具有这种嵌套基因结构的同源常染色体通过抑制同源重组与当时已经分化的性染色体融合。随着性染色体分化扩展到融合区域,一对同源的AMEL基因也分两步彼此分化;首先在5'区域(内含子2中转座子MER5的启动子区域),然后在其余的3'区域。这导致了真兽类性染色体中配子同源的AMELX和AMELY。虽然AMELX和AMELY之间5'区域的早期分化与AMELY较低的表达水平一致,但没有迹象表明AMELY在氨基酸水平上发生了退化。相反,特定谱系中的AMELX和AMELY都可能经历正选择,随后是负选择以保留已确立的功能。基于人类群体中AMELX和AMELY多态性的模式和水平,也有人认为AMELX附近的重组冷点可能与古代拟常染色体边界的成因有关。