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枯草芽孢杆菌芽孢形成过程中吞噬蛋白的双重定位途径。

Dual localization pathways for the engulfment proteins during Bacillus subtilis sporulation.

作者信息

Aung Stefan, Shum Jonathan, Abanes-De Mello Angelica, Broder Dan H, Fredlund-Gutierrez Jennifer, Chiba Shinobu, Pogliano Kit

机构信息

Division of Biological Sciences, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0377, USA.

出版信息

Mol Microbiol. 2007 Sep;65(6):1534-46. doi: 10.1111/j.1365-2958.2007.05887.x.

Abstract

Engulfment in Bacillus subtilis is mediated by two complementary systems, SpoIID, SpoIIM and SpoIIP (DMP), which are essential for engulfment, and the SpoIIQ-SpoIIIAGH (Q-AH) zipper, which provides a secondary engulfment mechanism and recruits other proteins to the septum. We here identify two mechanisms by which DMP localizes to the septum. The first depends on SpoIIB, which is recruited to the septum during division and provides a septal landmark for efficient DMP localization. However, sporangia lacking SpoIIB ultimately localize DMP and complete engulfment, suggesting a second mechanism for DMP localization. This secondary targeting pathway depends on SpoIVFA and SpoIVFB, which are recruited to the septum by the Q-AH zipper. The absence of a detectable localization phenotype in mutants lacking only SpoIVFAB (or Q-AH) suggests that SpoIIB provides the primary DMP localization pathway while SpoIVFAB provides a secondary pathway. In keeping with this hypothesis, the spoIIB spoIVFAB mutant strain has a synergistic engulfment defect at septal thinning (which requires DMP) and is completely defective in DMP localization. Thus, the Q-AH zipper both provides a compensatory mechanism for engulfment when DMP activity is reduced, and indirectly provides a compensatory mechanism for septal localization of DMP when its primary targeting pathway is disrupted.

摘要

枯草芽孢杆菌中的吞噬作用由两个互补系统介导,即SpoIID、SpoIIM和SpoIIP(DMP),它们对吞噬作用至关重要,以及SpoIIQ-SpoIIIAGH(Q-AH)拉链,它提供了一种辅助吞噬机制并将其他蛋白质招募到隔膜处。我们在此确定了DMP定位于隔膜的两种机制。第一种机制依赖于SpoIIB,它在细胞分裂期间被招募到隔膜处,并为DMP的有效定位提供隔膜标记。然而,缺乏SpoIIB的芽孢囊最终会定位DMP并完成吞噬作用,这表明存在DMP定位的第二种机制。这种辅助靶向途径依赖于SpoIVFA和SpoIVFB,它们由Q-AH拉链招募到隔膜处。在仅缺乏SpoIVFAB(或Q-AH)的突变体中未检测到定位表型,这表明SpoIIB提供了主要的DMP定位途径,而SpoIVFAB提供了次要途径。与该假设一致,spoIIB spoIVFAB突变株在隔膜变薄(这需要DMP)时具有协同吞噬缺陷,并且在DMP定位方面完全有缺陷。因此,Q-AH拉链在DMP活性降低时既提供了吞噬作用的补偿机制,又在其主要靶向途径被破坏时间接提供了DMP隔膜定位的补偿机制。

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