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染色体重排产生一个发育转录因子的复合基因。

Chromosomal rearrangement generating a composite gene for a developmental transcription factor.

作者信息

Stragier P, Kunkel B, Kroos L, Losick R

机构信息

Department of Cellular and Developmental Biology, Harvard University, Cambridge, MA 02138.

出版信息

Science. 1989 Jan 27;243(4890):507-12. doi: 10.1126/science.2536191.

Abstract

Differential gene expression in the mother cell chamber of sporulating cells of Bacillus subtilis is determined in part by an RNA polymerase sigma factor called sigma K (or sigma 27). The sigma K factor was assigned as the product of the sporulation gene spoIVCB on the basis of the partial aminoterminal amino acid sequence of the purified protein. The spoIVCB gene is now shown to be a truncated gene capable of specifying only the amino terminal half of sigma K. The carboxyl terminal half is specified by another sporulation gene, spoIIIC, to which spoIVCB becomes joined inframe at an intermediate stage of sporulation by site-specific recombination within a 5-base pair repeated sequence. Juxtaposition of spoIVCB and spoIIIC need not be reversible in that the mother cell and its chromosome are discarded at the end of the developmental cycle. The rearrangement of chromosomal DNA could account for the presence of sigma K selectively in the mother cell and may be a precedent for the generation of cell type-specific regulatory proteins in other developmental systems where cells undergo terminal differentiation.

摘要

枯草芽孢杆菌芽孢形成细胞母细胞腔中的差异基因表达部分由一种名为σK(或σ27)的RNA聚合酶σ因子决定。基于纯化蛋白的部分氨基末端氨基酸序列,σK因子被指定为芽孢形成基因spoIVCB的产物。现在表明spoIVCB基因是一个截短的基因,仅能指定σK的氨基末端一半。羧基末端一半由另一个芽孢形成基因spoIIIC指定,在芽孢形成的中间阶段,spoIVCB通过5个碱基对重复序列内的位点特异性重组与spoIIIC读框内连接。spoIVCB和spoIIIC的并置不一定是可逆的,因为在发育周期结束时母细胞及其染色体被丢弃。染色体DNA的重排可以解释σK仅在母细胞中的存在,并且可能是其他细胞经历终末分化的发育系统中产生细胞类型特异性调节蛋白的先例。

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