Shyue S K, Boissinot S, Schneider H, Sampaio I, Schneider M P, Abee C R, Williams L, Hewett-Emmett D, Sperling H G, Cowing J A, Dulai K S, Hunt D M, Li W H
Human Genetics Center, School of Public Health, University of Texas, P.O. Box 20334, Houston, TX 77225, USA.
J Mol Evol. 1998 Jun;46(6):697-702. doi: 10.1007/pl00006350.
Although most New World monkeys have only one X-linked photopigment locus, many species have three polymorphic alleles at the locus. The three alleles in the squirrel monkey and capuchin have spectral peaks near 562, 550, and 535 nm, respectively, and the three alleles in the marmoset and tamarin have spectral peaks near 562, 556, and 543 nm, respectively. To determine the amino acids responsible for the spectral sensitivity differences among these pigment variants, we sequenced all exons of the three alleles in each of these four species. From the deduced amino acid sequences and the spectral peak information and from previous studies of the spectral tuning of X-linked pigments in humans and New World monkeys, we estimated that the Ala --> Ser, Ile --> Phe, Gly --> Ser, Phe --> Tyr, and Ala --> Tyr substitutions at residue positions 180, 229, 233, 277, and 285, respectively, cause spectral shifts of about 5, -2, -1, 8, and 15 nm. On the other hand, the substitutions His --> Tyr, Met --> Val or Leu, and Ala --> Tyr at positions 116, 275, and 276, respectively, have no discernible spectral tuning effect, though residues 275 and 276 are inside the transmembrane domains. Many substitutions between Val and Ile or between Val and Ala have occurred in the transmembrane domains among the New World monkey pigment variants but apparently have no effect on spectral tuning. Our study suggests that, in addition to amino acid changes involving a hydroxyl group, large changes in residue size can also cause a spectral shift in a visual pigment.
尽管大多数新大陆猴只有一个X连锁的视色素基因座,但许多物种在该基因座上有三个多态性等位基因。松鼠猴和卷尾猴的三个等位基因的光谱峰值分别接近562、550和535纳米,狨猴和绢毛猴的三个等位基因的光谱峰值分别接近562、556和543纳米。为了确定导致这些色素变体光谱敏感性差异的氨基酸,我们对这四个物种中每个物种的三个等位基因的所有外显子进行了测序。根据推导的氨基酸序列、光谱峰值信息以及之前对人类和新大陆猴X连锁色素光谱调谐的研究,我们估计,分别在残基位置180、229、233、277和285处的丙氨酸→丝氨酸、异亮氨酸→苯丙氨酸、甘氨酸→丝氨酸、苯丙氨酸→酪氨酸和丙氨酸→酪氨酸取代,会导致约5、-2、-1、8和15纳米的光谱位移。另一方面,分别在位置116、275和276处的组氨酸→酪氨酸、甲硫氨酸→缬氨酸或亮氨酸以及丙氨酸→酪氨酸取代,没有明显的光谱调谐效应,尽管残基275和276位于跨膜结构域内。在新大陆猴色素变体的跨膜结构域中,缬氨酸和异亮氨酸之间或缬氨酸和丙氨酸之间发生了许多取代,但显然对光谱调谐没有影响。我们的研究表明,除了涉及羟基的氨基酸变化外,残基大小的大幅变化也会导致视觉色素的光谱位移。