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小鼠主要组织相容性复合体中的一个非多态性I类基因。

A nonpolymorphic class I gene in the murine major histocompatibility complex.

作者信息

Mellor A L, Weiss E H, Kress M, Jay G, Flavell R A

出版信息

Cell. 1984 Jan;36(1):139-44. doi: 10.1016/0092-8674(84)90082-5.

Abstract

DNA sequence analysis of a class I gene (Q10), which maps to the Qa2,3 locus in the C57BL/10 (H-2b haplotype) mouse, reveals that it is almost identical to a cDNA clone (pH16) isolated from a SWR/J (H-2q haplotype) mouse liver cDNA library. Exon 5, in particular, has an unusual structure such that a polypeptide product is unlikely to be anchored in the cell membrane. Our findings suggest that the two sequences are derived from allelic class I genes, which are nonpolymorphic, in contrast to H-2K allelic sequences from the same mice, and they may encode liver-specific polypeptides of unknown function. Our previous studies indicate that the Q10 gene is a potential donor gene for the generation of mutations at the H-2K locus by inter-gene transfer of genetic information. Thus the lack of polymorphism in class I genes at the Q10 locus implies either that they are not recipients for such exchanges or that selective pressure prevents the accumulation of mutations in genes at this locus.

摘要

对一个I类基因(Q10)进行DNA序列分析,该基因定位于C57BL/10(H-2b单倍型)小鼠的Qa2,3位点,结果显示它与从SWR/J(H-2q单倍型)小鼠肝脏cDNA文库中分离出的一个cDNA克隆(pH16)几乎完全相同。特别是外显子5具有不寻常的结构,以至于不太可能有一个多肽产物锚定在细胞膜上。我们的研究结果表明,这两个序列源自等位I类基因,与同一小鼠的H-2K等位基因序列不同,它们是非多态性的,并且可能编码功能未知的肝脏特异性多肽。我们之前的研究表明,Q10基因是通过基因间遗传信息转移在H-2K位点产生突变的潜在供体基因。因此,Q10位点I类基因缺乏多态性意味着要么它们不是此类交换的接受者,要么选择压力阻止了该位点基因中突变的积累。

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