The Aspergillus nidulans esdC (early sexual development) gene is necessary for sexual development and is controlled by veA and a heterotrimeric G protein
The esdC ( early sexual development) gene was isolated by using an expressed sequence tag (EST) as a probe from a genomic library of the early sexual developmental stage mycelia of Aspergillus nidulans. The sequence analysis revealed that the esdC gene contains a 59 bp intron and encodes a 266 amino...
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Veröffentlicht in: | Fungal genetics and biology 2008-03, Vol.45 (3), p.310-318 |
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Zusammenfassung: | The
esdC (
early
sexual
development) gene was isolated by using an expressed sequence tag (EST) as a probe from a genomic library of the early sexual developmental stage mycelia of
Aspergillus nidulans. The sequence analysis revealed that the
esdC gene contains a 59
bp intron and encodes a 266 amino acid polypeptide with a calculated molecular weight of 29.4
kDa. The EsdC protein is conserved among filamentous fungi and has a domain with similarity to a glycogen binding domain conserved in the β subunit of the AMP-activated protein kinase (AMPK) complex. Although the
esdD gene was expressed during asexual development, the expression reached its maximum at 10
h and decreased thereafter up to 50
h after the end of the induction of sexual development. In an
esdC-null mutant under a
veA
+ background, no sexual structures were formed at any condition examined. However,
esdC overexpression did not lead to an induction of sexual development. In addition, to the effect of the
esdC mutation on the sexual development, more conidiophores were formed in the
esdC-null mutant than in a wild type. These results indicate that the
esdC gene is necessary for sexual structure formation but its overexpression is not sufficient to enhance this process. Expression of the
esdC gene throughout development was positively regulated by the
veA gene. In addition, very little and no
esdC transcript, respectively, was observed in an
flbA-null mutant and in a
fadA
G42R mutant, and the
esdC transcript level was higher in a
fadA-null mutant and in a
sfaD-null mutant than in a wild type, indicating that inactivation of FadA is necessary for positive regulation of
esdC expression. |
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ISSN: | 1087-1845 1096-0937 |
DOI: | 10.1016/j.fgb.2007.09.008 |