Evidence that metabolism and chromosome copy number control mutually exclusive cell fates in Bacillus subtilis

被引:63
作者
Chai, Yunrong [1 ]
Norman, Thomas [1 ]
Kolter, Roberto [2 ]
Losick, Richard [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
Bacillus subtilis; Biofilm; chromosome copy number; metabolic control; COMPLETE GENOME SEQUENCE; BIOFILM FORMATION; MASTER REGULATOR; SPO0A REGULON; SPORULATION; SIGNAL; REPLICATION; INITIATION; PROTEIN; SWITCH;
D O I
10.1038/emboj.2011.36
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacillus subtilis chooses between matrix production and spore formation, which are both controlled by the regulator Spo0A similar to P. We report that metabolism and chromosome copy number dictate which fate is adopted. Conditions that favour low Spo0A similar to P levels promote matrix production, whereas conditions favouring high levels trigger sporulation. Spo0A similar to P directs the synthesis of SinI, an antirepressor for the SinR repressor of matrix genes. The regulatory region of sinI contains an activator site that Spo0A similar to P binds strongly and operators that bind Spo0A similar to P weakly. Evidence shows that low Spo0A similar to P levels turn sinI ON and high levels turn sinI OFF and instead switch sporulation ON. Cells in which sinI and sinR were transplanted from their normal position near the chromosome replication terminus to positions near the origin and cells that harboured an extra copy of the genes were blocked in matrix production. Thus, matrix gene expression is sensitive to the number of copies of sinI and sinR. Because cells at the start of sporulation have two chromosomes and matrix-producing cells one, chromosome copy number could contribute to cell-fate determination. The EMBO Journal (2011) 30, 1402-1413. doi: 10.1038/emboj.2011.36; Published online 15 February 2011
引用
收藏
页码:1402 / 1413
页数:12
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