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人类淀粉酶基因的协同进化

Concerted evolution of human amylase genes.

作者信息

Gumucio D L, Wiebauer K, Caldwell R M, Samuelson L C, Meisler M H

机构信息

Department of Human Genetics, University of Michigan, Ann Arbor 48109-0618.

出版信息

Mol Cell Biol. 1988 Mar;8(3):1197-205. doi: 10.1128/mcb.8.3.1197-1205.1988.

Abstract

Cosmid clones containing 250 kilobases of genomic DNA from the human amylase gene cluster have been isolated. These clones contain seven distinct amylase genes which appear to comprise the complete multigene family. By sequence comparison with the cDNAs, we have identified two pancreatic amylase genes and three salivary amylase genes. Two truncated pseudogenes were also recovered. Intergenic distances of 17 to 22 kilobases separate the amylase gene copies. Within the past 10 million years, duplications, gene conversions, and unequal crossover events have resulted in a very high level of sequence similarity among human amylase gene copies. To identify sequence elements involved in tissue-specific expression and hormonal regulation, the promoter regions of the human amylase genes were sequenced and compared with those of the corresponding mouse genes. The promoters of the human and mouse pancreatic amylase genes are highly homologous between nucleotide -160 and the cap site. Two sequence elements thought to influence pancreas-specific expression of the rodent genes are present in the human genes. In contrast, similarity in the 5' flanking sequences of the salivary amylase genes is limited to several short sequence elements whose positions and orientations differ in the two species. Some of these sequence elements are also associated with other parotid-specific genes and may be involved in their tissue-specific expression. A glucocorticoid response element and a general enhancer element are closely associated in several of the amylase promoters.

摘要

已分离出包含来自人类淀粉酶基因簇250千碱基基因组DNA的黏粒克隆。这些克隆含有七个不同的淀粉酶基因,它们似乎构成了完整的多基因家族。通过与cDNA进行序列比较,我们鉴定出了两个胰腺淀粉酶基因和三个唾液淀粉酶基因。还回收了两个截短的假基因。17至22千碱基的基因间距离分隔了淀粉酶基因拷贝。在过去的1000万年中,重复、基因转换和不等交换事件导致人类淀粉酶基因拷贝之间具有非常高的序列相似性。为了鉴定参与组织特异性表达和激素调节的序列元件,对人类淀粉酶基因的启动子区域进行了测序,并与相应的小鼠基因的启动子区域进行了比较。人类和小鼠胰腺淀粉酶基因的启动子在核苷酸-160与帽位点之间高度同源。人类基因中存在两个被认为影响啮齿动物基因胰腺特异性表达的序列元件。相比之下,唾液淀粉酶基因5'侧翼序列的相似性仅限于几个短序列元件,其在两个物种中的位置和方向不同。其中一些序列元件也与其他腮腺特异性基因相关,可能参与它们的组织特异性表达。糖皮质激素反应元件和一个通用增强子元件在几个淀粉酶启动子中紧密相连。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e6/363264/a2df00836187/molcellb00063-0200-a.jpg

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