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牛细胞角蛋白序列在三条染色体上四个不同位点的定位。

Mapping of bovine cytokeratin sequences to four different sites on three chromosomes.

作者信息

Fries R, Threadgill D W, Hediger R, Gunawardana A, Blessing M, Jorcano J L, Stranzinger G, Womack J E

机构信息

Department of Animal Sciences, Federal Institute of Technology, ETH-Zentrum, Zürich, Switzerland.

出版信息

Cytogenet Cell Genet. 1991;57(2-3):135-41. doi: 10.1159/000133132.

Abstract

The chromosomal location of bovine class I and class II cytokeratin sequences was determined using in situ hybridization and Southern blot hybridization to DNA from hybrid somatic cells. The main signals were found over chromosome region 19q16----qter after in situ hybridization with two probes for the class I cytokeratin gene subfamily (KRT10 and KRT19) and over region 5q14----q23 after hybridization with probes for the class II gene subfamily (KRT1, KRT5, and KRT8). These regions most likely contain the loci of functional cytokeratin genes, with KRT10 and KRT19 mapping to 19q21 and KRT1, KRT5, and KRT8 to 5q21. The in situ hybridization data were corroborated by analysis of a somatic hybrid cell panel. The genes for the class I keratins segregated concordantly with each other and syntenic group U21 but were discordant with the class II keratin genes. The class II keratin genes segregated concordantly with each other and syntenic group U3. Two class II gene probes gave an additional minor signal above chromosome region 5q25----q33 after in situ hybridization, while another class II probe yielded a minor signal above chromosome region 10q31----qter. When the latter probe and an additional linked probe were hybridized to DNAs from a hybrid panel, two independently segregating loci were recognized, one of which cosegregated with the class II subfamily in syntenic group U3 and the other with syntenic group U5. These data confirm the chromosomal assignment of two syntenic groups and allow the assignment of a formerly unassigned syntenic group.

摘要

利用原位杂交和对杂交体细胞DNA进行Southern印迹杂交的方法,确定了牛I类和II类细胞角蛋白序列的染色体定位。用I类细胞角蛋白基因亚家族的两种探针(KRT10和KRT19)进行原位杂交后,主要信号出现在染色体区域19q16----qter;用II类基因亚家族的探针(KRT1、KRT5和KRT8)杂交后,主要信号出现在区域5q14----q23。这些区域很可能包含功能性细胞角蛋白基因的位点,其中KRT10和KRT19定位于19q21,KRT1、KRT5和KRT8定位于5q21。对一个体细胞杂交细胞系的分析证实了原位杂交的数据。I类角蛋白基因彼此之间以及与同线群U21共分离,但与II类角蛋白基因不共分离。II类角蛋白基因彼此之间以及与同线群U3共分离。两种II类基因探针在原位杂交后,在染色体区域5q25----q33上方产生了一个额外的次要信号,而另一种II类探针在染色体区域10q31----qter上方产生了一个次要信号。当后一种探针和一个额外的连锁探针与杂交细胞系的DNA杂交时,识别出两个独立分离的位点,其中一个与同线群U3中的II类亚家族共分离,另一个与同线群U5共分离。这些数据证实了两个同线群的染色体定位,并允许对一个以前未定位的同线群进行定位。

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