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PMID: 3157864 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Isolation and characterization of genes differentially expressed during conidiation of Neurospora crassa.

Molecular and cellular biology ·Vol. 5 ·No. 4 ·1985-04-00 ·Pages 849-55

Berlin V, Yanofsky C

Abstract

A Neurospora crassa genomic DNA library was screened with a cDNA probe enriched in sequences expressed in conidiating cultures. Clones were isolated that preferentially hybridized to this probe versus a second cDNA probe complementary to polyadenylated RNA isolated from mycelia. Twelve clones contained unique sequences that hybridized to 22 transcripts, 19 of which accumulated preferentially in conidiating cultures. Eight transcripts were present in higher levels in conidiating cultures than in mycelia. Eleven transcripts were detected only in conidiating cultures and first appeared at different times during the asexual cycle. We mapped genomic sequences homologous to the 11 clones by conventional crosses using restriction fragment-length polymorphisms as genetic markers. The sequences homologous to genes expressed preferentially in conidiating cultures are distributed on six of the seven chromosomes. Clones that map to the same chromosome are linked. No recombination occurred between genomic sequences homologous to three clones, suggesting that the genes contained in these clones may constitute a gene cluster.

MeSH Terms
Cell Differentiation Chromosome Mapping Cloning, Molecular Fungal Proteins/genetics Gene Expression Regulation Genes, Fungal Neurospora/genetics Neurospora crassa/genetics RNA, Messenger/genetics Transcription, Genetic
Chemicals
Fungal Proteins RNA, Messenger
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Berlin V
Yanofsky C
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1985-04-00
Pages
849-55
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC366790
Subset
IM
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