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牛纤连蛋白和γ-晶状体蛋白基因的体细胞定位与限制性片段分析。

Somatic cell mapping and restriction fragment analysis of bovine genes for fibronectin and gamma crystallin.

作者信息

Adkison L R, Skow L C, Thomas T L, Petrash M, Womack J E

机构信息

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

出版信息

Cytogenet Cell Genet. 1988;47(3):155-9. doi: 10.1159/000132536.

Abstract

DNAs from cow-hamster and cow-mouse somatic hybrid cells segregating bovine chromosomes have been analyzed by Southern blotting and hybridization with human fibronectin and gamma crystallin probes. Concordancy of retention of these bovine genes was compared to cattle isozyme loci representing previously described syntenic groups. Bovine fibronectin (FNI) and gamma crystallin (CRYG) fragments were concordant with each other and with isocitrate dehydrogenase 1 (IDH1), representing the bovine syntenic group U17. The syntenic relationship of these genes is conserved on human chromosome 2q and also on mouse chromosome 1. In addition, bovine RFLPs were identified with both fibronectin and gamma crystallin probes. These polymorphisms will be used to study recombination between the syntenic loci in pedigreed herds and to mark a segment of the bovine genome that is likely homologous to the Lsh region of mouse chromosome 1, which confers resistance in mice to several intracellular parasites.

摘要

通过Southern印迹法以及与人纤连蛋白和γ-晶状体蛋白探针杂交,对来自分离牛染色体的牛-仓鼠和牛-小鼠体细胞杂种细胞的DNA进行了分析。将这些牛基因保留的一致性与代表先前描述的同线群的牛同工酶基因座进行了比较。牛纤连蛋白(FNI)和γ-晶状体蛋白(CRYG)片段彼此一致,并且与代表牛同线群U17的异柠檬酸脱氢酶1(IDH1)一致。这些基因的同线关系在人类2号染色体以及小鼠1号染色体上都是保守的。此外,用纤连蛋白和γ-晶状体蛋白探针都鉴定出了牛的限制性片段长度多态性(RFLP)。这些多态性将用于研究纯种牛群中同线基因座之间的重组,并标记牛基因组中可能与小鼠1号染色体Lsh区域同源的一个片段,该区域赋予小鼠对几种细胞内寄生虫的抗性。

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