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日本男性红绿色觉色素基因的分子模式与序列多态性

Molecular patterns and sequence polymorphisms in the red and green visual pigment genes of Japanese men.

作者信息

Deeb S S, Alvarez A, Malkki M, Motulsky A G

机构信息

Department of Medicine, University of Washington, Seattle 98195, USA.

出版信息

Hum Genet. 1995 May;95(5):501-6. doi: 10.1007/BF00223860.

Abstract

The red-green pigment gene arrays of 203 (101 from a previous study and 102 from this study) randomly selected men of Japanese ancestry from the Seattle area were screened for the abnormal molecular patterns (deletions and red/green or green/red hybrid genes) that are usually associated with defective color vision. Such molecular patterns were found in approximately 5% of these individuals, which is equivalent to the frequency of phenotypic color vision defects in Japanese males in Japan. Thus, the majority of hybrid genes carried by Japanese males appear to be associated with defective color vision. In contrast, the frequency of hybrid genes among Caucasians and African-Americans is approximately two and five times the frequency of color vision defects in these two ethnic groups, respectively. The coding sequences of 50 males of Japanese ancestry were determined. All the polymorphisms in the red and green pigment genes that were detected in the Japanese sample had been observed in Caucasians and African-Americans. The same polymorphisms of the red pigment gene were present in the green pigment gene, suggesting that gene conversion contributes to sequence homogenization between these pigment genes. As is the case for Caucasians, exon 3 of the red and green pigment genes was observed to be a hot spot for recombination and gene conversion. Fewer polymorphic sites (4 vs 11) and haplotypes (5 vs 14) of the red pigment gene were observed in Japanese than in Caucasians. The Japanese population was more uniform with respect to the red pigment gene, with 70% of individuals having the same haplotype, as compared with the 43% for the Caucasian population. This difference was largely due to the lower degree of polymorphism at position 180 of the red pigment gene in Japanese (84% Ser and 16% Ala vs 62% Ser and 38% Ala.) The number of polymorphic sites and haplotypes in the green pigment gene was similar in the two populations. Nevertheless, the Japanese population was more uniform with 65% having the same haplotype. The difference in the frequency of alleles at position 283 accounted for this difference in haplotype distribution.

摘要

对来自西雅图地区的203名(101名来自先前研究,102名来自本研究)随机选择的日本裔男性的红绿色素基因阵列进行筛查,以寻找通常与色觉缺陷相关的异常分子模式(缺失以及红/绿或绿/红杂交基因)。在大约5%的这些个体中发现了此类分子模式,这与日本国内日本男性表型色觉缺陷的频率相当。因此,日本男性携带的大多数杂交基因似乎与色觉缺陷有关。相比之下,白种人和非裔美国人中杂交基因的频率分别约为这两个种族色觉缺陷频率的两倍和五倍。测定了50名日本裔男性的编码序列。在日本样本中检测到的红绿色素基因中的所有多态性在白种人和非裔美国人中都已被观察到。红色素基因的相同多态性也存在于绿色素基因中,这表明基因转换有助于这些色素基因之间的序列同质化。与白种人一样,红色素基因和绿色素基因的外显子3被观察到是重组和基因转换的热点。在日本人中观察到的红色素基因的多态性位点(4个对11个)和单倍型(5个对14个)比白种人少。日本人群在红色素基因方面更为一致,70%的个体具有相同的单倍型,而白种人群体为43%。这种差异主要是由于日本人红色素基因第180位的多态性程度较低(84%为丝氨酸和16%为丙氨酸,而白种人为62%丝氨酸和38%丙氨酸)。两个群体中绿色素基因的多态性位点和单倍型数量相似。然而,日本人群体更为一致,65%的个体具有相同的单倍型。第283位等位基因频率的差异导致了单倍型分布的这种差异。

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