The Neurospora aab-1 gene encodes a CCAAT Binding Protein Homologous to Yeast HAP5

Author:

Chen Huaxian1,Crabb John W2,Kinsey John A1

Affiliation:

1. Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas 66160

2. W. Alton Jones Cell Science Center, Inc., Lake Placid, New York 12946

Abstract

Abstract The expression of the am (glutamate dehydrogenase) gene is dependent upon two upstream activating sequences, designated URSamα and URSamβ. A heteromeric nuclear protein Am  Alpha Binding protein (AAB) binds specifically to a CCAAT box within the URSamα element. AAB appears to be composed of three components. We used polyclonal antiserum raised against the highly purified AAB1 subunit to isolate a partial aab-1 cDNA clone, which was then used to isolate a full-length cDNA and a genomic clone. The full-length cDNA has the potential to encode a 272 amino acid protein with a calculated molecular weight of 30 kD. Amino acid sequence obtained by Edman analysis of the AAB1 protein confirmed that the aab-1 gene had been cloned. AAB-1 shows similarity to the HAP5 protein of yeast and the CBF-C protein of rat. Each of these proteins is an essential subunit of their respective heteromeric CCAAT binding proteins. The aab1 gene maps on linkage group III of Neurospora crassa near the trp-1 locus. Disruption of the aab-1 gene results in pleiotropic effects on growth and development as well as a 50% reduction in glutamate dehydrogenase levels. Transformation of the aab-1 disruption mutant strain with the cloned genomic copy of the aab-1 gene rescued all of the phenotypic alterations associated with the aab-1 mutation.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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5. Sequential gel mobility shift scanning of 5′ upstream sequences of the Neurospora crassa am (GDH) gene;Chen;Mol. Gen. Genet.,1994

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