Evidence map›Paper›PMID 26463163›Full record

ArticlemBio2015

Direct target network of the Neurospora crassa plant cell wall deconstruction regulators CLR-1, CLR-2, and XLR-1.

James P Craig, Samuel T Coradetti, Trevor L Starr, N Louise Glass

Open access · goldAbstract read
In one paragraph

Article in mBio, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
15.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 112 citations in OpenAlex.

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  13. The CBS/HCommunications biology · 2024
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  16. Regulation of nutrient utilization in filamentous fungi.Applied microbiology and biotechnology · 2023
    Review
  17. Article
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  20. Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

James P CraigDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, USA Energy Biosciences Institute, University of California, Berkeley, Berkeley, California, USA Chan Soon-Shiong Institute of Molecular Medicine, Windber, Pennsylvania, USA.
Samuel T CoradettiDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, USA Energy Biosciences Institute, University of California, Berkeley, Berkeley, California, USA Buck Institute for Research on Aging, Novato, California, USA.
Trevor L StarrDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, USA Energy Biosciences Institute, University of California, Berkeley, Berkeley, California, USA Dupont Industrial Biosciences, Palo Alto, California, USA.
N Louise GlassDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, USA Energy Biosciences Institute, University of California, Berkeley, Berkeley, California, USA Lglass@berkeley.edu.
University of California, Berkeley · US

Funding

POSTGRADUATE TRAINING PROGRAM IN GENETICST32GM007127 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DILLIN, ANDREW G · 1985 to 2016
$7.9M
NIGMS NIH HHS 2 T32 GM7127-36 A1NIGMS NIH HHS T32 GM007127
6 · The paper itself

Abstract

unlabelledFungal deconstruction of the plant cell requires a complex orchestration of a wide array of intracellular and extracellular enzymes. In Neurospora crassa, CLR-1, CLR-2, and XLR-1 have been identified as key transcription factors regulating plant cell wall degradation in response to soluble sugars. The XLR-1 regulon was defined using a constitutively active mutant allele, resulting in hemicellulase gene expression and secretion under noninducing conditions. To define genes directly regulated by CLR-1, CLR-2, and XLR-1, we performed chromatin immunoprecipitation and next-generation sequencing (ChIPseq) on epitope-tagged constructs of these three transcription factors. When N. crassa is exposed to plant cell wall material, CLR-1, CLR-2, and XLR-1 individually bind to the promoters of the most strongly induced genes in their respective regulons. These include promoters of genes encoding cellulases for CLR-1 and CLR-2 (CLR-1/CLR-2) and promoters of genes encoding hemicellulases for XLR-1. CLR-1 bound to its regulon under noninducing conditions; however, this binding alone did not translate into gene expression and enzyme secretion. Motif analysis of the bound genes revealed conserved DNA binding motifs, with the CLR-2 motif matching that of its closest paralog in Saccharomyces cerevisiae, Gal4p. Coimmunoprecipitation studies showed that CLR-1 and CLR-2 act in a homocomplex but not as a CLR-1/CLR-2 heterocomplex. IMPORTANCE: Understanding fungal regulation of complex plant cell wall deconstruction pathways in response to multiple environmental signals via interconnected transcriptional circuits provides insight into fungus/plant interactions and eukaryotic nutrient sensing. Coordinated optimization of these regulatory networks is likely required for optimal microbial enzyme production.

Indexed as

Gene Expression RegulationGene Regulatory NetworksAmino Acid MotifsBinding SitesCarbohydratesCellulasesChromatin ImmunoprecipitationCytosolDNA-Binding ProteinsDNA, ProtozoanNeurospora crassaPlant CellsPromoter Regions, GeneticProtein BindingProtozoan ProteinsRegulonCarbohydratesCellulasesDNA-Binding ProteinsDNA, ProtozoanProtozoan Proteins

Identifiers

PMID26463163
PMCPMC4620465
OpenAlexW2175879646

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.