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Originally published as Genetics Published Articles Ahead of Print on April 3, 2007.

Genetics, Vol. 176, 243-253, May 2007, Copyright © 2007
doi:10.1534/genetics.106.068239

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basA Regulates Cell Wall Organization and Asexual/Sexual Sporulation Ratio in Aspergillus nidulans

Shaojie Li*,1, Dapeng Bao*,1, Gary Yuen{dagger}, Steve D. Harris{dagger} and Ana M. Calvo*,2

* Department of Biological Sciences, Northern Illinois University, DeKalb, Illinois 60115 and {dagger} Department of Plant Pathology, University of Nebraska, Lincoln, Nebraska 68588-0660

2 Corresponding author: Department of Biological Sciences, 1425 W. Lincoln Highway, Montomery Hall Bldg., Northern Illinois University, DeKalb, IL 60115.
E-mail: amcalvo{at}niu.edu

Sphingolipid C4 hydroxylase catalyzes the conversion of dihydrosphingosine to phytosphingosine. In Saccharomyces cerevisiae, Sur2 is essential for sphingolipid C4 hydroxylation activity but not essential for normal growth. Here we demonstrate that the Aspergillus nidulans Sur2 homolog BasA is also required for phytosphingosine biosynthesis but is also essential for viability. We previously reported that a point missense mutation in basA resulted in aberrant cell wall thickening. Here our data suggest that accumulation of dihydrosphingosine is responsible for this phenotype. In addition, two different mutations in basA consistently accelerated the transition from asexual development to sexual development compared to the wild-type strain. The phenotype could be suppressed by exogenous addition of phytosphingosine. Northern analysis suggests that faster sexual development in the basA mutant might be due to a higher transcription level of ppoA and steA, genes demonstrated to coordinate a balance between asexual and sexual development in A. nidulans. Consistent with these findings, mutations in the ceramide-synthase-encoding genes barA and lagA also caused faster transition from asexual to sexual development, supporting the involvement of sphingolipid metabolism in fungal morphogenesis.




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C. Simenel, B. Coddeville, M. Delepierre, J.-P. Latge, and T. Fontaine
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[Abstract] [Full Text] [PDF]




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