Carbon catabolite repression of the Aspergillus nidulans xlnA gene.

Abstract:

:Expression of the Aspergillus nidulans 22 kDa endoxylanase gene, xlnA, is controlled by at least three mechanisms: specific induction by xylan or xylose; carbon catabolite repression (CCR); and regulation by ambient pH. Deletion analysis of xlnA upstream sequences has identified two positively acting regions: one that mediates specific induction by xylose; and another that mediates the influence of ambient pH and contains two PacC consensus binding sites. The extreme derepressed mutation creAd30 results in considerable, although not total, loss of xlnA glucose repressibility, indicating a major role for CreA in its CCR. Three consensus CreA binding sites are present upstream of the structural gene. Point mutational analysis using reporter constructs has identified a single site, xlnA.C1, that is responsible for direct CreA repression in vivo. Using the creAd30 derepressed mutant background, our results indicate the existence of indirect repression by CreA.

journal_name

Mol Microbiol

journal_title

Molecular microbiology

authors

Orejas M,MacCabe AP,Pérez González JA,Kumar S,Ramón D

doi

10.1046/j.1365-2958.1999.01157.x

subject

Has Abstract

pub_date

1999-01-01 00:00:00

pages

177-84

issue

1

eissn

0950-382X

issn

1365-2958

journal_volume

31

pub_type

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