Literature DB >> 2412092

Changes in gene expression elicited by amino acid limitation in Neurospora crassa strains having normal or mutant cross-pathway amino acid control.

H J Flint.   

Abstract

The effects of amino acid limitation on gene expression have been investigated in Neurospora crassa strains carrying normal (cpc-1+) or mutant (cpc-1) alleles at a locus implicated in cross-pathway amino acid control. Electrophoresis and fluorography were used to reveal the patterns of label incorporation into polypeptides in vivo, or after in vitro translation of extracted mRNAs. In a cpc-1+ strain at least 20% of detectable in vitro translation products showed relative increases in incorporation when RNA was obtained from mycelium grown under conditions of arginine limitation, by comparison with conditions of arginine sufficiency. A cpc-1 mutation, which impairs derepression of a variety of amino acid synthetic enzymes following amino acid limitation, had little detectable effect on in vivo polypeptide synthesis during amino acid sufficient growth or following pyrimidine limitation. However the mutation substantially altered the response to arginine or histidine limitation. The majority of in vitro translation products that showed increased expression in arginine limited cpc-1+ failed to increase in cpc-1 strains, but arginine limitation of cpc-1 also resulted in increases that did not occur in cpc-1+ strains. This may reflect both direct and indirect consequences of the impairment of cross-pathway control.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2412092     DOI: 10.1007/bf00425437

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  23 in total

1.  Genetics of arginine biosynthesis in Neurospora crassa.

Authors:  R H Davis
Journal:  Genetics       Date:  1979-11       Impact factor: 4.562

2.  The suppression of defective translation by ppGpp and its role in the stringent response.

Authors:  P H O'Farrell
Journal:  Cell       Date:  1978-07       Impact factor: 41.582

3.  A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamide gels.

Authors:  W M Bonner; R A Laskey
Journal:  Eur J Biochem       Date:  1974-07-01

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  General control of arginine biosynthetic enzymes in Neurospora crassa.

Authors:  H J Flint; B F Kemp
Journal:  J Gen Microbiol       Date:  1981-05

6.  Noncoordinated transcription in the absence of protein synthesis in yeast.

Authors:  R W Shulman; C E Sripati; J R Warner
Journal:  J Biol Chem       Date:  1977-02-25       Impact factor: 5.157

7.  Cloning of the am (glutamate dehydrogenase) gene of Neurospora crassa through the use of a synthetic DNA probe.

Authors:  J H Kinnaird; M A Keighren; J A Kinsey; M Eaton; J R Fincham
Journal:  Gene       Date:  1982-12       Impact factor: 3.688

8.  Polyphosphate-cation interaction in the amino acid-containing vacuole of Neurospora crassa.

Authors:  C L Cramer; R H Davis
Journal:  J Biol Chem       Date:  1984-04-25       Impact factor: 5.157

9.  Regulation of tryptophan biosynthesis in Saccharomyces cerevisiae: mode of action of 5-methyl-tryptophan and 5-methyl-tryptophan-sensitive mutants.

Authors:  A Schürch; J Miozzari; R Hütter
Journal:  J Bacteriol       Date:  1974-03       Impact factor: 3.490

10.  Positive regulation in the general amino acid control of Saccharomyces cerevisiae.

Authors:  A G Hinnebusch; G R Fink
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

View more
  12 in total

1.  Deprivation of a single amino acid induces protein synthesis-dependent increases in c-jun, c-myc, and ornithine decarboxylase mRNAs in Chinese hamster ovary cells.

Authors:  P Pohjanpelto; E Hölttä
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

Review 2.  Mechanisms of gene regulation in the general control of amino acid biosynthesis in Saccharomyces cerevisiae.

Authors:  A G Hinnebusch
Journal:  Microbiol Rev       Date:  1988-06

3.  The cross-pathway control gene of Neurospora crassa, cpc-1, encodes a protein similar to GCN4 of yeast and the DNA-binding domain of the oncogene v-jun-encoded protein.

Authors:  J L Paluh; M J Orbach; T L Legerton; C Yanofsky
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

4.  Regulation of amino acid synthetic enzymes in Neurospora crassa in the presence of high concentrations of amino acids.

Authors:  I B Barthelmess
Journal:  Mol Gen Genet       Date:  1986-06

5.  Transcriptional activation of a cycloheximide-inducible gene encoding laccase is mediated by cpc-1, the cross-pathway control gene, in Neurospora crassa.

Authors:  H Tamaru; T Nishida; T Harashima; H Inoue
Journal:  Mol Gen Genet       Date:  1994-06-03

6.  Identification and characterization of four new GCD genes in Saccharomyces cerevisiae.

Authors:  P Niederberger; M Aebi; R Hütter
Journal:  Curr Genet       Date:  1986       Impact factor: 3.886

7.  Cloning of the arg-12 gene of Neurospora crassa and regulation of its transcript via cross-pathway amino acid control.

Authors:  H J Flint; J Wilkening
Journal:  Mol Gen Genet       Date:  1986-04

8.  Isolation and characterization of mutants defective in production of laccase in Neurospora crassa.

Authors:  A Zamma; H Tamaru; T Harashima; H Inoue
Journal:  Mol Gen Genet       Date:  1993-08

9.  cpc-1, the general regulatory gene for genes of amino acid biosynthesis in Neurospora crassa, is differentially expressed during the asexual life cycle.

Authors:  D J Ebbole; J L Paluh; M Plamann; M S Sachs; C Yanofsky
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

10.  Transcriptional profiling of cross pathway control in Neurospora crassa and comparative analysis of the Gcn4 and CPC1 regulons.

Authors:  Chaoguang Tian; Takao Kasuga; Matthew S Sachs; N Louise Glass
Journal:  Eukaryot Cell       Date:  2007-04-20
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.