Reversal of an epigenetic switch governing cell chaining in Bacillus subtilis by protein instability.

Abstract:

:Bacillus subtilis forms long chains of cells during growth and biofilm formation. Cell separation is mediated by autolysins, whose genes are under the negative control of a heteromeric complex composed of the proteins SinR and SlrR. Formation of the SinR-SlrR complex is governed by a self-reinforcing, double-negative feedback loop in which SinR represses the gene for SlrR and SlrR, by forming the SinR-SlrR complex, titrates SinR and prevents it from repressing slrR. The loop is a bistable switch and exists in a SlrR(LOW) state in which autolysin genes are on, and a SlrR(HIGH) state in which autolysin genes are repressed by SinR-SlrR. Cells in the SlrR(LOW) state are driven into the SlrR(HIGH) state by SinI, an antirepressor that binds to and inhibits SinR. However, the mechanism by which cells in the SlrR(HIGH) state revert back to the SlrR(LOW) state is unknown. We report that SlrR is proteolytically unstable and present evidence that self-cleavage via a LexA-like autopeptidase and ClpC contribute to its degradation. Cells producing a self-cleavage-resistant mutant of SlrR exhibited more persistent chaining during growth and yielded biofilms with enhanced structural complexity. We propose that degradation of SlrR allows cells to switch from the SlrR(HIGH) to the SlrR(LOW) state.

journal_name

Mol Microbiol

journal_title

Molecular microbiology

authors

Chai Y,Kolter R,Losick R

doi

10.1111/j.1365-2958.2010.07335.x

subject

Has Abstract

pub_date

2010-10-01 00:00:00

pages

218-29

issue

1

eissn

0950-382X

issn

1365-2958

journal_volume

78

pub_type

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