Premium
The HAP2,3,4 transcriptional activator is required for derepression of the yeast citrate synthase gene, CIT1
Author(s) -
Rosenkrantz Mark,
Keil Christine S.,
Pennell Elizabeth A.,
Devenish Louise J.
Publication year - 1994
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.1994.tb00407.x
Subject(s) - derepression , biology , gene , activator (genetics) , microbiology and biotechnology , genetics , psychological repression , gene expression
Summary The yeast nuclear gene CIT1 encodes mitochondrial citrate synthase, which catalyses the first and rate‐limiting step of the tricarboxylic acid (TCA) cycle. Transcription of CIT1 is subject to glucose repression. Mutations in HAP2, HAP3 or HAP4 block derepression of a CIT1‐lacZ gene fusion. The HAP2,3,4 transcriptional activator also activates nuclear genes encoding components of the mitochondrial electron transport chain, and thus it co‐ordinates derepression of two major mitochondrial functions. Two DNA sequences resembling the consensus HAP2,3,4‐binding site (ACCAATNA) are located at approximately‐ 310 and ‐290, upstream of the CIT1 coding sequence. Deletion and mutation analysis indicates that the 290 element is critical for activation by HAP2,3,4. Glucose‐repressed expression of CIT1 is largely independent of HAP2,3,4, is repressed by glutamate, and requires a DNA sequence between ‐367 and ‐348. Evidence is presented for a second HAP2,3,4‐independent activation element located just upstream and overlapping the ‐290 HAP2,3,4 element.