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中国仓鼠ESD和rRNA基因的表达及区域定位,这些基因与导致中国仓鼠卵巢细胞中Z1和Z6染色体易位相关。

Expression and regional assignment of Chinese hamster ESD and rRNA genes associated with translocations giving rise to chromosomes Z1 and Z6 in CHO cells.

作者信息

Stallings R L, Adair G M, Lin J C, Siciliano M J

出版信息

Cytogenet Cell Genet. 1984;38(2):132-7. doi: 10.1159/000132045.

Abstract

The Chinese hamster genes ADK, NP, ESD, PGM2, PEPS, PEPB, GLO, and GSR, all of which are on Chinese hamster chromosome 1, were assigned to CHO-LA chromosomes by analysis of the segregation of CHO isozymes and chromosomes from interspecific somatic cell hybrids made with CHO cells and mouse C11D cells. One allele of each of these eight loci remained linked on the normal chromosome 1 homolog. For seven loci, the other allele remained linked on chromosome Z1, but ESD was shown to have been translocated to chromosome Z6 (Chinese hamster chromosome 5q +). Ag-NOR staining of CHO chromosomes indicated that the (1;5) translocation was very likely reciprocal, since the Chinese hamster chromosome 5, which gave rise to the CHO Z6, lacks an NOR and the Z1 now has one. These data allowed regional assignment of ESD to the distal portion of Chinese hamster chromosome 1p and provided genetic evidence for the origin of CHO chromosomes Z1 and Z6 from Chinese hamster chromosomes 1 and 5. Induced electrophoretic shift mutations of ESD and positive Ag-NOR staining for the rRNA genes on the Z1 showed that the activities of the genes lying close to the translocation breakpoints were maintained.

摘要

中国仓鼠的ADK、NP、ESD、PGM2、PEPS、PEPB、GLO和GSR基因均位于中国仓鼠的1号染色体上,通过分析中国仓鼠同工酶和染色体在中国仓鼠卵巢细胞(CHO)与小鼠C11D细胞形成的种间体细胞杂种中的分离情况,将这些基因定位到CHO-LA染色体上。这八个基因座的每个基因座的一个等位基因仍与正常的1号染色体同源物连锁。对于七个基因座,另一个等位基因仍与Z1染色体连锁,但ESD已被证明易位到Z6染色体(中国仓鼠5号染色体长臂)。对CHO染色体的银染核仁组织区(Ag-NOR)染色表明,(1;5)易位很可能是相互的,因为产生CHO Z6的中国仓鼠5号染色体缺乏核仁组织区,而Z1现在有一个。这些数据允许将ESD区域定位到中国仓鼠1号染色体短臂的远端,并为CHO染色体Z1和Z6源自中国仓鼠染色体1和5提供了遗传学证据。ESD的诱导电泳迁移突变以及Z1上rRNA基因的阳性Ag-NOR染色表明,靠近易位断点的基因活性得以维持。

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