A branched pathway governing the activation of a developmental transcription factor by regulated intramembrane proteolysis.

Abstract:

:The proteolytic activation of the membrane-associated transcription factor pro-sigma(K) is controlled by a signal transduction pathway during sporulation in the bacterium Bacillus subtilis. The pro-sigma(K) processing enzyme SpoIVFB, a membrane-embedded metalloprotease, is held inactive by two other integral-membrane proteins, SpoIVFA and BofA. We demonstrate that the signaling protease SpoIVB (IVB) triggers pro-sigma(K) processing by cleaving the extracellular domain of the SpoIVFA regulator at multiple sites. In vitro, these cleavages do not disrupt the interactions between SpoIVFA, SpoIVFB, and BofA, suggesting that IVB-dependent activation of the processing enzyme results from a conformational change in this complex. Our data further suggest that when IVB is unable to cleave SpoIVFA, it can still activate pro-sigma(K) processing through a second protease, CtpB. Finally, we demonstrate that CtpB, like IVB, triggers pro-sigma(K) processing by cleaving SpoIVFA. We propose that IVB regulates intramembrane proteolysis through two proteolytic pathways, both of which converge on the same regulator.

journal_name

Mol Cell

journal_title

Molecular cell

authors

Campo N,Rudner DZ

doi

10.1016/j.molcel.2006.05.019

subject

Has Abstract

pub_date

2006-07-07 00:00:00

pages

25-35

issue

1

eissn

1097-2765

issn

1097-4164

pii

S1097-2765(06)00334-0

journal_volume

23

pub_type

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