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基因产物在柄杆菌细胞分化过程中的定位。

Positioning of gene products during Caulobacter cell differentiation.

作者信息

Shapiro L, Gober J W

机构信息

Department of Microbiology, College of Physicians & Surgeons, Columbia University, New York, NY 10032.

出版信息

J Cell Sci Suppl. 1989;11:85-97. doi: 10.1242/jcs.1989.supplement_11.7.

DOI:10.1242/jcs.1989.supplement_11.7
PMID:2693463
Abstract

Caulobacter crescentus has one of the simplest known developmental programs that exhibits both temporal and spatial organization. A hallmark of the Caulobacter cell cycle is that the progeny cells that result from each cell division differ from one another with respect to structure and developmental program. The process of establishing asymmetry prior to cell division requires that a number of gene products be targeted to a pole of the predivisional cell and consequently segregated to one of the two progeny. Several products involved in flagellar biogenesis and the chemotaxis machinery are segregated to the swarmer cell. Evidence suggests that the protein product of some fla and che genes is targeted to the incipient swarmer cell pole. In the case of other flagellar genes, it is the mRNA that is apparently segregated to the swarmer cell. Two heat shock proteins, DnaK and Lon are specifically segregated to the progeny stalked cell.

摘要

新月柄杆菌具有已知最简单的发育程序之一,该程序展现出时间和空间组织。柄杆菌细胞周期的一个标志是,每次细胞分裂产生的子代细胞在结构和发育程序方面彼此不同。在细胞分裂前建立不对称性的过程要求许多基因产物被靶向到分裂前细胞的一个极,从而被分配到两个子代细胞之一。一些参与鞭毛生物合成和趋化机制的产物被分配到游动细胞。有证据表明,一些鞭毛(fla)基因和趋化(che)基因的蛋白质产物被靶向到初始游动细胞极。对于其他鞭毛基因,显然是mRNA被分配到游动细胞。两种热休克蛋白,DnaK和Lon,特异性地被分配到子代柄细胞。

相似文献

1
Positioning of gene products during Caulobacter cell differentiation.基因产物在柄杆菌细胞分化过程中的定位。
J Cell Sci Suppl. 1989;11:85-97. doi: 10.1242/jcs.1989.supplement_11.7.
2
Differential expression and positioning of chemotaxis methylation proteins in Caulobacter.趋化甲基化蛋白在柄杆菌中的差异表达与定位
J Mol Biol. 1984 Sep 25;178(3):551-68. doi: 10.1016/0022-2836(84)90238-9.
3
Regulation of cellular differentiation in Caulobacter crescentus.新月柄杆菌中细胞分化的调控
Microbiol Rev. 1995 Mar;59(1):31-47. doi: 10.1128/mr.59.1.31-47.1995.
4
Asymmetric segregation of heat-shock proteins upon cell division in Caulobacter crescentus.
J Mol Biol. 1987 Apr 20;194(4):653-62. doi: 10.1016/0022-2836(87)90242-7.
5
A sigma 54 transcriptional activator also functions as a pole-specific repressor in Caulobacter.一个σ54转录激活因子在柄杆菌中也作为一种极特异性阻遏物发挥作用。
Genes Dev. 1994 Aug 1;8(15):1839-52. doi: 10.1101/gad.8.15.1839.
6
Plasmid and chromosomal DNA replication and partitioning during the Caulobacter crescentus cell cycle.新月柄杆菌细胞周期中的质粒和染色体DNA复制及分配
J Mol Biol. 1990 Apr 20;212(4):709-22. doi: 10.1016/0022-2836(90)90232-B.
7
Cell cycle-controlled proteolysis of a flagellar motor protein that is asymmetrically distributed in the Caulobacter predivisional cell.鞭毛马达蛋白的细胞周期控制的蛋白水解作用,该蛋白在新月柄杆菌分裂前细胞中不对称分布。
EMBO J. 1996 May 15;15(10):2393-406.
8
Positional information during Caulobacter cell differentiation.柄杆菌细胞分化过程中的位置信息。
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The control of spatial organization during cellular differentiation.细胞分化过程中空间组织的调控。
Cell Mol Biol Res. 1994;40(3):199-205.
10
Requirement of the carboxyl terminus of a bacterial chemoreceptor for its targeted proteolysis.细菌化学感受器羧基末端靶向蛋白水解的要求。
Science. 1993 Mar 19;259(5102):1754-7. doi: 10.1126/science.8456303.

引用本文的文献

1
Regulatory interactions between phospholipid synthesis and DNA replication in Caulobacter crescentus.新月柄杆菌中磷脂合成与DNA复制之间的调控相互作用。
J Bacteriol. 1990 Oct;172(10):5523-30. doi: 10.1128/jb.172.10.5523-5530.1990.
2
Purification and characterization of fatty acid beta-oxidation enzymes from Caulobacter crescentus.新月柄杆菌脂肪酸β-氧化酶的纯化与特性分析
J Bacteriol. 1990 Feb;172(2):997-1004. doi: 10.1128/jb.172.2.997-1004.1990.
3
Escherichia coli ribonucleotide reductase expression is cell cycle regulated.
大肠杆菌核糖核苷酸还原酶的表达受细胞周期调控。
Mol Biol Cell. 1992 Oct;3(10):1095-105. doi: 10.1091/mbc.3.10.1095.
4
Early Caulobacter crescentus genes fliL and fliM are required for flagellar gene expression and normal cell division.早期新月柄杆菌基因fliL和fliM是鞭毛基因表达和正常细胞分裂所必需的。
J Bacteriol. 1992 May;174(10):3327-38. doi: 10.1128/jb.174.10.3327-3338.1992.