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啮齿动物组蛋白H2a假基因进化的比较分析。

Comparative analysis of evolution in a rodent histone H2a pseudogene.

作者信息

DeBry R W

机构信息

Department of Biological Sciences, University of Cincinnati, OH 45221-0006, USA.

出版信息

J Mol Evol. 1998 Mar;46(3):355-60. doi: 10.1007/pl00006312.

Abstract

Sequences were obtained from five species of rodents that are orthologous to an H2a histone pseudogene from Mus musculus. The pseudogene is part of the cluster of replication-dependent histone genes found on Mus musculus chromosome 13. Comparative analysis of these five sequences together with the previously published sequence from M. musculus shows that this gene has likely been a pseudogene throughout the evolution of the genus Mus, while the gene from Rattus norvegicus is likely functional. Three large (> 20 bp) deletions were found among the Mus pseudogenes, a feature that is very unusual compared to surveys of processed pseudogenes. In addition, there are two single-base deletions and one 4-bp insertion among the Mus pseudogenes. The species distributions of one of the large deletions and the 4-bp insertion require either independent insertions of an identical sequence, independent deletions with identical boundaries, or a deletion followed by precise reintegration of the original sequence. The evidence favors the hypothesis of multiple deletions with identical boundaries. The "coding" regions of the Mus pseudogenes show a much reduced level of among-species variability in the 3' half of the pseudogene, compared both to the 5' half and to flanking sequences. This supports a hypothesis that the 3' end of the pseudogene is the target of frequent gene conversion by functional H2a genes.

摘要

从五种啮齿动物中获得了与小家鼠H2a组蛋白假基因直系同源的序列。该假基因是小家鼠13号染色体上发现的复制依赖型组蛋白基因簇的一部分。将这五个序列与先前发表的小家鼠序列进行比较分析表明,在小家鼠属的整个进化过程中,该基因可能一直是假基因,而褐家鼠的该基因可能具有功能。在小家鼠假基因中发现了三个大的(>20 bp)缺失,与加工假基因的调查相比,这一特征非常不寻常。此外,小家鼠假基因中还有两个单碱基缺失和一个4 bp的插入。其中一个大缺失和4 bp插入的物种分布需要相同序列的独立插入、具有相同边界的独立缺失,或者是一个缺失后原始序列的精确重新整合。证据支持具有相同边界的多个缺失的假说。小家鼠假基因的“编码”区域在假基因3'端的物种间变异性水平与5'端和侧翼序列相比大幅降低。这支持了一个假说,即假基因的3'端是功能性H2a基因频繁基因转换的目标。

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