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对“破布”(一种X连锁显性发育性小鼠突变)的基因分析。

Genetic analyses of tattered, an X-linked dominant, developmental mouse mutation.

作者信息

Merrell K, Gonzales J C, Wells S, Calame K, Herman G E

机构信息

Integrated Program in Molecular Biology and Cellular Biophysics, Columbia College of Physicians and Surgeons, New York, New York, USA.

出版信息

Mamm Genome. 1995 Apr;6(4):291-4. doi: 10.1007/BF00352419.

Abstract

Tattered (Td) is an X-linked dominant mouse mutation that causes prenatal lethality in affected males. To map the locus, we analyzed 199 normal male and affected female progeny from a backcross of Td and Mus castaneus. Pedigree analysis of these animals suggests a gene order of cen-DXWas70-(Td, DXMit26, Gata1, Tcfe3)-(Cybb, Otc)-tel, where Tcfe3 is a transcription factor homologous to a gene involved in the murine microphthalmia (mi) mutation [Hodgkinson et al. Cell 74, 395-404, 1993]. To evaluate Tcfe3 as a candidate for Td, heterozygous tattered females were crossed to xid males to obtain females in which > 95% of B cells expressed genes solely from the Td X Chromosome (Chr). Fluorescent activated cell sorting (FACS) analysis and Western blotting of isolated splenocytes from Td/xid double heterozygotes rule out Tcfe3 as a likely candidate for the Td mutation.

摘要

破布(Td)是一种X连锁显性小鼠突变,会导致受影响的雄性小鼠在产前死亡。为了定位该基因座,我们分析了来自Td与栗色小鼠回交的199只正常雄性和受影响的雌性后代。对这些动物的系谱分析表明基因顺序为着丝粒-DXWas70-(Td、DXMit26、Gata1、Tcfe3)-(Cybb、Otc)-端粒,其中Tcfe3是一种转录因子,与参与小鼠小眼症(mi)突变的基因同源[霍奇金森等人。《细胞》74卷,395 - 404页,1993年]。为了评估Tcfe3作为Td的候选基因,将杂合的破布雌性小鼠与xid雄性小鼠杂交,以获得其中超过95%的B细胞仅表达来自Td X染色体(Chr)基因的雌性小鼠。对Td/xid双杂合子分离的脾细胞进行荧光激活细胞分选(FACS)分析和蛋白质免疫印迹,排除了Tcfe3作为Td突变可能候选基因的可能性。

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