Keyword search (4,163 papers available)

"transcriptomics" Keyword-tagged Publications:

Title Authors PubMed ID
1 A Bacteroides synthetic biology toolkit to build an in vivo malabsorption biosensor McCallum G; Burckhardt JC; He J; Hong A; Potvin-Trottier L; Tropini C; 41610848
BIOLOGY
2 An examination of the quinic acid utilization genes in Aspergillus niger reveals the involvement of two pH-dependent permeases Sgro M; Reid ID; Arentshorst M; Ram AFJ; Tsang A; 40853219
GENOMICS
3 em Candida albicans /em : a historical overview of investigations into an important human pathogen Shrivastava M; Whiteway M; 40522159
BIOLOGY
4 Transcriptomics identify the triggering of citrate export as the key event caused by manganese deficiency in Aspergillus niger Fekete E; Bíró V; Márton A; Bakondi-Kovács I; Sándor E; Kovács B; Geoffrion N; Tsang A; Kubicek CP; Karaffa L; 39377610
CSFG
5 Functional analysis of the protocatechuate branch of the β-ketoadipate pathway in Aspergillus niger Sgro M; Chow N; Olyaei F; Arentshorst M; Geoffrion N; Ram AFJ; Powlowski J; Tsang A; 37399977
BIOLOGY
6 Identification of Genes Involved in the Degradation of Lignocellulose Using Comparative Transcriptomics Gruninger RJ; Tsang A; McAllister TA; 37149538
CSFG
7 An Evolutionarily Conserved Transcriptional Activator-Repressor Module Controls Expression of Genes for D-Galacturonic Acid Utilization in Aspergillus niger. Niu J, Alazi E, Reid ID, Arentshorst M, Punt PJ, Visser J, Tsang A, Ram AF 28049705
CSFG
8 Identification of Genes Involved in the Degradation of Lignocellulose Using Comparative Transcriptomics. Gruninger RJ, Reid I, Forster RJ, Tsang A, McAllister TA 28417376
CSFG
9 Introduction: Overview of Fungal Genomics. de Vries RP, Grigoriev IV, Tsang A 29876804
CSFG

 

Title:An Evolutionarily Conserved Transcriptional Activator-Repressor Module Controls Expression of Genes for D-Galacturonic Acid Utilization in Aspergillus niger.
Authors:Niu JAlazi EReid IDArentshorst MPunt PJVisser JTsang ARam AF
Link:https://www.ncbi.nlm.nih.gov/pubmed/28049705?dopt=Abstract
DOI:10.1534/genetics.116.194050
Publication:Genetics
Keywords:galacturonic acidgene regulationgenomicspectinrepressor proteintranscriptomics
PMID:28049705 Category:Genetics Date Added:2019-06-07
Dept Affiliation: CSFG
1 Molecular Microbiology and Biotechnology, Leiden University, Institute of Biology Leiden, 2333 BE Leiden, The Netherlands.
2 Centre for Structural and Functional Genomics, Concordia University, Montreal, Quebec H4B1R6, Canada.
3 Dutch DNA Biotech, 3704 HE Zeist, Utrecht, The Netherlands.
4 Molecular Microbiology and Biotechnology, Leiden University, Institute of Biology Leiden, 2333 BE Leiden, The Netherlands a.f.j.ram@biology.leidenuniv.nl.

Description:

An Evolutionarily Conserved Transcriptional Activator-Repressor Module Controls Expression of Genes for D-Galacturonic Acid Utilization in Aspergillus niger.

Genetics. 2017 01;205(1):169-183

Authors: Niu J, Alazi E, Reid ID, Arentshorst M, Punt PJ, Visser J, Tsang A, Ram AF

Abstract

The expression of genes encoding extracellular polymer-degrading enzymes and the metabolic pathways required for carbon utilization in fungi are tightly controlled. The control is mediated by transcription factors that are activated by the presence of specific inducers, which are often monomers or monomeric derivatives of the polymers. A D-galacturonic acid-specific transcription factor named GaaR was recently identified and shown to be an activator for the expression of genes involved in galacturonic acid utilization in Botrytis cinerea and Aspergillus niger Using a forward genetic screen, we isolated A. niger mutants that constitutively express GaaR-controlled genes. Reasoning that mutations in the gaaR gene would lead to a constitutively activated transcription factor, the gaaR gene in 11 of the constitutive mutants was sequenced, but no mutations in gaaR were found. Full genome sequencing of five constitutive mutants revealed allelic mutations in one particular gene encoding a previously uncharacterized protein (NRRL3_08194). The protein encoded by NRRL3_08194 shows homology to the repressor of the quinate utilization pathway identified previously in Neurospora crassa (qa-1S) and Aspergillus nidulans (QutR). Deletion of NRRL3_08194 in combination with RNA-seq analysis showed that the NRRL3_08194 deletion mutant constitutively expresses genes involved in galacturonic acid utilization. Interestingly, NRRL3_08194 is located next to gaaR (NRRL3_08195) in the genome. The homology to the quinate repressor, the chromosomal clustering, and the constitutive phenotype of the isolated mutants suggest that NRRL3_08194 is likely to encode a repressor, which we name GaaX. The GaaR-GaaX module and its chromosomal organization is conserved among ascomycetes filamentous fungi, resembling the quinate utilization activator-repressor module in amino acid sequence and chromosomal organization.

PMID: 28049705 [PubMed - indexed for MEDLINE]





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