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ATF-1 transcription factor regulates the expression of ccg-1 and cat-1 genes in response to fludioxonil under OS-2 MAP kinase in Neurospora crassa

The ATF/CREB family transcriptional factors are regulated by stress-activated MAP kinase in yeast. The disruptants of the atf-1 gene, which encodes an ATF/CREB family transcriptional factor, were isolated and characterized in Neurospora crassa. The characteristic phenotypes in the os-2 MAP kinase st...

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Published in:Fungal genetics and biology 2008-12, Vol.45 (12), p.1562-1569
Main Authors: Yamashita, Kazuhiro, Shiozawa, Azusa, Watanabe, Setsuko, Fukumori, Fumiyasu, Kimura, Makoto, Fujimura, Makoto
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cited_by cdi_FETCH-LOGICAL-c472t-708496622215b36a37f418803a9546026c98f059070e42505e26705472ad27543
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container_title Fungal genetics and biology
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creator Yamashita, Kazuhiro
Shiozawa, Azusa
Watanabe, Setsuko
Fukumori, Fumiyasu
Kimura, Makoto
Fujimura, Makoto
description The ATF/CREB family transcriptional factors are regulated by stress-activated MAP kinase in yeast. The disruptants of the atf-1 gene, which encodes an ATF/CREB family transcriptional factor, were isolated and characterized in Neurospora crassa. The characteristic phenotypes in the os-2 MAP kinase strain, such as osmotic sensitivity and fludioxonil resistance, were not observed in the Δ atf-1 strain; however, like the os-2 strain, up-regulation of the catalase gene cat-1 and the clock-controlled gene ccg-1 by treatment with fludioxonil (1 μg/mL) or 4% NaCl was almost completely abolished in the Δ atf-1 strain. A gel shift assay indicated that ATF-1 bound to the cat-1 and ccg-1 promoters probably through the CRE motifs. The enzyme activity of large-subunit catalase CAT-1, the major conidial catalase, was not detected in the Δ atf-1 strain, suggesting that the production of CAT-1 during formation of conidia is largely dependent on ATF-1. Among 11 clock-controlled genes, the expression of ccg-1, ccg-9, ccg-13, and ccg-14 was induced by fludioxonil in an OS-2-dependent manner; however, induction of ccg-13 and ccg-14 was observed in the Δ atf-1 strain, suggesting the existence of another transcription factor regulated by OS-2. The homozygous cross between the Δ atf-1 strains produced perithecia and ascospores; however, their ascospores never germinated. These findings suggest that ATF-1 acts as one of the transcriptional factors downstream of the OS-2 MAP kinase and probably regulates some genes involved in conidiation, circadian rhythm, and ascospore maturation in N. crassa.
doi_str_mv 10.1016/j.fgb.2008.09.012
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The disruptants of the atf-1 gene, which encodes an ATF/CREB family transcriptional factor, were isolated and characterized in Neurospora crassa. The characteristic phenotypes in the os-2 MAP kinase strain, such as osmotic sensitivity and fludioxonil resistance, were not observed in the Δ atf-1 strain; however, like the os-2 strain, up-regulation of the catalase gene cat-1 and the clock-controlled gene ccg-1 by treatment with fludioxonil (1 μg/mL) or 4% NaCl was almost completely abolished in the Δ atf-1 strain. A gel shift assay indicated that ATF-1 bound to the cat-1 and ccg-1 promoters probably through the CRE motifs. The enzyme activity of large-subunit catalase CAT-1, the major conidial catalase, was not detected in the Δ atf-1 strain, suggesting that the production of CAT-1 during formation of conidia is largely dependent on ATF-1. Among 11 clock-controlled genes, the expression of ccg-1, ccg-9, ccg-13, and ccg-14 was induced by fludioxonil in an OS-2-dependent manner; however, induction of ccg-13 and ccg-14 was observed in the Δ atf-1 strain, suggesting the existence of another transcription factor regulated by OS-2. The homozygous cross between the Δ atf-1 strains produced perithecia and ascospores; however, their ascospores never germinated. 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The disruptants of the atf-1 gene, which encodes an ATF/CREB family transcriptional factor, were isolated and characterized in Neurospora crassa. The characteristic phenotypes in the os-2 MAP kinase strain, such as osmotic sensitivity and fludioxonil resistance, were not observed in the Δ atf-1 strain; however, like the os-2 strain, up-regulation of the catalase gene cat-1 and the clock-controlled gene ccg-1 by treatment with fludioxonil (1 μg/mL) or 4% NaCl was almost completely abolished in the Δ atf-1 strain. A gel shift assay indicated that ATF-1 bound to the cat-1 and ccg-1 promoters probably through the CRE motifs. The enzyme activity of large-subunit catalase CAT-1, the major conidial catalase, was not detected in the Δ atf-1 strain, suggesting that the production of CAT-1 during formation of conidia is largely dependent on ATF-1. Among 11 clock-controlled genes, the expression of ccg-1, ccg-9, ccg-13, and ccg-14 was induced by fludioxonil in an OS-2-dependent manner; however, induction of ccg-13 and ccg-14 was observed in the Δ atf-1 strain, suggesting the existence of another transcription factor regulated by OS-2. The homozygous cross between the Δ atf-1 strains produced perithecia and ascospores; however, their ascospores never germinated. 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The disruptants of the atf-1 gene, which encodes an ATF/CREB family transcriptional factor, were isolated and characterized in Neurospora crassa. The characteristic phenotypes in the os-2 MAP kinase strain, such as osmotic sensitivity and fludioxonil resistance, were not observed in the Δ atf-1 strain; however, like the os-2 strain, up-regulation of the catalase gene cat-1 and the clock-controlled gene ccg-1 by treatment with fludioxonil (1 μg/mL) or 4% NaCl was almost completely abolished in the Δ atf-1 strain. A gel shift assay indicated that ATF-1 bound to the cat-1 and ccg-1 promoters probably through the CRE motifs. The enzyme activity of large-subunit catalase CAT-1, the major conidial catalase, was not detected in the Δ atf-1 strain, suggesting that the production of CAT-1 during formation of conidia is largely dependent on ATF-1. Among 11 clock-controlled genes, the expression of ccg-1, ccg-9, ccg-13, and ccg-14 was induced by fludioxonil in an OS-2-dependent manner; however, induction of ccg-13 and ccg-14 was observed in the Δ atf-1 strain, suggesting the existence of another transcription factor regulated by OS-2. The homozygous cross between the Δ atf-1 strains produced perithecia and ascospores; however, their ascospores never germinated. These findings suggest that ATF-1 acts as one of the transcriptional factors downstream of the OS-2 MAP kinase and probably regulates some genes involved in conidiation, circadian rhythm, and ascospore maturation in N. crassa.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18948219</pmid><doi>10.1016/j.fgb.2008.09.012</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 1087-1845
ispartof Fungal genetics and biology, 2008-12, Vol.45 (12), p.1562-1569
issn 1087-1845
1096-0937
language eng
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source ScienceDirect Freedom Collection
subjects Antifungal Agents - pharmacology
ascospores
ATF-1 gene
biochemical mechanisms
Catalase
catalase-1 gene
Circadian rhythm
clock-controlled-1 gene
conidia
Dioxoles - pharmacology
DNA, Fungal - metabolism
Electrophoretic Mobility Shift Assay
enzyme activity
enzymes
fludioxonil
Fungal Proteins - biosynthesis
fungus physiology
Gene Deletion
Gene Expression Regulation, Fungal
genes
MAP kinase
mitogen-activated protein kinase
molds (fungi)
Mutagenesis, Insertional
Neurospora crassa
Neurospora crassa - genetics
Neurospora crassa - physiology
osmotolerance
Phosphotransferases
Promoter Regions, Genetic
Protein Binding
Pyrroles - pharmacology
signal transduction
transcription factors
Transcription Factors - genetics
Transcription Factors - metabolism
transcriptional activation
Two-component signal transduction
title ATF-1 transcription factor regulates the expression of ccg-1 and cat-1 genes in response to fludioxonil under OS-2 MAP kinase in Neurospora crassa
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