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人类铁蛋白H假基因中的保守突变:是第二个功能序列还是进化怪象?

Conserved mutations in human ferritin H pseudogenes: a second functional sequence or an evolutionary quirk?

作者信息

Zheng H, Bhavsar D, Dugast I, Zappone E, Drysdale J

机构信息

Department of Biochemistry, Tufts School of Medicine, Boston, MA 02111, USA.

出版信息

Biochim Biophys Acta. 1997 Mar 20;1351(1-2):150-6. doi: 10.1016/s0167-4781(96)00188-1.

Abstract

This paper describes a search for a second functional human ferritin H gene in a collection of genomic clones. Nine new H-like sequences have been mapped to chromosomes 1p22-31, 1q32-42, 2q32-33, 3q21-23, 13q12, 14, 17p11-pter and X. These were examined for evidence of possible functionality by sequencing and by searching for possible introns. All except an uncharacterized sequence on chromosome 13 appear to be processed pseudogenes. However, nearly all share several conserved differences with the known functional sequence. These differences occur at regions of unusual structure. It is not known whether these sequences are derived from a second functional gene or from site-specific mutations in the generation of pseudogenes from the known functional gene. We also show that several hominoids contain H gene families with similar complexities to humans and that most of the human genes have counterparts in chimpanzees and gorillas.

摘要

本文描述了在一组基因组克隆中寻找第二个功能性人类铁蛋白H基因的过程。九个新的H样序列已被定位到染色体1p22 - 31、1q32 - 42、2q32 - 33、3q21 - 23、13q12、14、17p11 - pter和X上。通过测序和寻找可能的内含子来检查这些序列是否有潜在功能的证据。除了13号染色体上一个未鉴定的序列外,其他所有序列似乎都是加工过的假基因。然而,几乎所有这些序列都与已知的功能序列有几个保守的差异。这些差异出现在结构异常的区域。尚不清楚这些序列是来自第二个功能基因,还是来自已知功能基因产生假基因过程中的位点特异性突变。我们还表明,几种类人猿含有与人类复杂性相似的H基因家族,并且大多数人类基因在黑猩猩和大猩猩中都有对应物。

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