Literature DB >> 191433

Inhibition of aminoacyl-transfer ribonucleic acid synthetases and the regulation of amino acid biosynthetic enzymes in Neurospora crassa.

S L Spurgeon, W H Matchett.   

Abstract

Growth conditions that result in the accumulation of the tryptophan intermediate indoleglycerol phosphate or of the histidine intermediate imidazoleglycerol phosphate cause mycelia of Neurospora crassa to exhibit an immediate and sustained increase in the differential rate at which the biosynthetic enzymes of the tryptophan, histidine, and arginine pathways are synthesized. These accumulated intermediates are shown to be inhibitors of the activity of aminoacyltransfer ribonucleic acid (tRNA) synthetases, as judged by an in vitro esterification assay. The tryptophan intermediate is shown to inhibit the charging of tryptophan, and the histidine intermediate is shown to inhibit charging of histidine. The inhibitions noted are consistent with the finding that the level of charged tRNATrp is decreased significantly in cells that have accumulated indoleglycerol phosphate and that of tRNAHis is decreased significantly in cells that have accumulated imidazoleglycerol phosphate. These results are interpreted as support for the involvement of aminoacyl-tRNA species in mediating cross-pathway regulation of the tryptophan, histidine, and arginine biosynthetic pathways as proposed in Lester's polyrepressor hypothesis (G. Lester, 1971). the correlations noted lead to the conclusion that Neurospora utilizes regulatory mechanisms that have the ability to react to changes in the level of charging of tRNA species.

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Year:  1977        PMID: 191433      PMCID: PMC235103          DOI: 10.1128/jb.129.3.1303-1312.1977

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  29 in total

1.  Integration of amino acid biosynthesis into the cell cycle of Saccharomyces cerevisiae.

Authors:  M Wolfner; D Yep; F Messenguy; G R Fink
Journal:  J Mol Biol       Date:  1975-08-05       Impact factor: 5.469

2.  THE CONVERSION OF SHIKIMIC ACID TO ANTHRANILIC ACID BY EXTRACTS OF NEUROSPORA CRASSA.

Authors:  J A DEMOSS
Journal:  J Biol Chem       Date:  1965-03       Impact factor: 5.157

3.  Studies on the mechanism of the tryptophan synthetase reaction.

Authors:  J A DEMOSS
Journal:  Biochim Biophys Acta       Date:  1962-08-13

4.  The biosynthesis of histidine; D-erythro-imidazoleglycerol phosphate dehydrase.

Authors:  B N AMES
Journal:  J Biol Chem       Date:  1957-09       Impact factor: 5.157

5.  The biosynthesis of histidine: imidazoleacetol phosphate transaminase.

Authors:  B N AMES; B L HORECKER
Journal:  J Biol Chem       Date:  1956-05       Impact factor: 5.157

6.  The biosynthesis of histidine; L-histidinol phosphate phosphatase.

Authors:  B N AMES
Journal:  J Biol Chem       Date:  1957-06       Impact factor: 5.157

7.  The enzymatic conversion of anthranilic acid to indole.

Authors:  C YANOFSKY
Journal:  J Biol Chem       Date:  1956-11       Impact factor: 5.157

8.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

9.  Inhibition of tryptophan synthetase by indoleacrylic acid.

Authors:  W H Matchett
Journal:  J Bacteriol       Date:  1972-04       Impact factor: 3.490

10.  INCREASED ACTIVITY OF TRYPTOPHAN BIOSYNTHETIC ENZYMES IN HISTIDINE MUTANTS OF NEUROSPORA CRASSA.

Authors:  M CARSIOTIS; A M LACY
Journal:  J Bacteriol       Date:  1965-06       Impact factor: 3.490

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  4 in total

Review 1.  Chromosomal loci of Neurospora crassa.

Authors:  D D Perkins; A Radford; D Newmeyer; M Björkman
Journal:  Microbiol Rev       Date:  1982-12

Review 2.  Control of growth and of the nuclear division cycle in Neurospora crassa.

Authors:  L Alberghina; E Sturani
Journal:  Microbiol Rev       Date:  1981-03

3.  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

4.  Circadian clock control of eIF2α phosphorylation is necessary for rhythmic translation initiation.

Authors:  Shanta Karki; Kathrina Castillo; Zhaolan Ding; Olivia Kerr; Teresa M Lamb; Cheng Wu; Matthew S Sachs; Deborah Bell-Pedersen
Journal:  Proc Natl Acad Sci U S A       Date:  2020-04-30       Impact factor: 11.205

  4 in total

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