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牛溶菌酶基因家族的物理图谱

Physical mapping of the lysozyme gene family in cattle.

作者信息

Gallagher D S, Threadgill D W, Ryan A M, Womack J E, Irwin D M

机构信息

Department of Veterinary Pathobiology, Texas A&M University, College Station 77843.

出版信息

Mamm Genome. 1993;4(7):368-73. doi: 10.1007/BF00360587.

Abstract

Amplification of an ancestral lysozyme gene in artiodactyls is associated with the evolution of foregut fermentation in the ruminant lineage and has resulted in about ten lysozyme genes in true ruminants. Hybridization of a cow stomach lysozyme 2 cDNA clone to restricted DNAs of a panel of cow x hamster hybrid cell lines revealed that all but one of the multiple bovine-specific bands segregate concordantly with the marker for bovine syntenic group U3 [Chromosome (Chr) 5]. The anomalous band was subsequently mapped to bovine syntenic group U22 (Chr 7) with a second panel of hybrids representing all 31 bovine syntenic groups. By two-dimensional pulsed-field gel electrophoresis the lysozyme genes on cattle Chr 5 were shown to be clustered on a 2- to 3-Mb DNA fragment, while the lactalbumin gene and pseudogenes that are paralogous and syntenic with the lysozymes were outside the lysozyme gene cluster. Chromosomal fluorescence in situ hybridization of a cocktail of lysozyme genomic clones localized the lysozyme gene cluster to cattle Chr 5 band 23, corroborating the somatic cell assignment.

摘要

偶蹄目动物中一个祖先溶菌酶基因的扩增与反刍动物谱系中前肠发酵的进化相关,并且在真正的反刍动物中产生了大约十个溶菌酶基因。用牛胃溶菌酶2 cDNA克隆与一组牛×仓鼠杂交细胞系的限制性DNA进行杂交,结果显示,除一条带外,多个牛特异性条带中的所有条带都与牛同线群U3[染色体(Chr)5]的标记一致分离。随后,利用代表所有31个牛同线群的另一组杂交细胞系,将这条异常条带定位到牛同线群U22(Chr 7)。通过二维脉冲场凝胶电泳显示,牛Chr 5上的溶菌酶基因聚集在一个2至3 Mb的DNA片段上,而与溶菌酶基因同源且同线的乳白蛋白基因和假基因则位于溶菌酶基因簇之外。用一组溶菌酶基因组克隆混合物进行染色体荧光原位杂交,将溶菌酶基因簇定位到牛Chr 5的23带,证实了体细胞定位结果。

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