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The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region.


ABSTRACT: In Neurospora crassa, the methionine synthase gene met-8 plays a key role in methionine synthesis. In this study, we found that MET-8 protein levels were compromised in several mutants defective in proper heterochromatin formation. Bioinformatics analysis revealed a 50-kb AT-rich region adjacent to the met-8 promoter. ChIP assays confirmed that trimethylated H3K9 was enriched in this region, indicating that heterochromatin may form upstream of met-8. In an H3K9R mutant strain, the output of met-8 was dramatically reduced, similar to what we observed in mutant strains that had defective heterochromatin formation. Furthermore, the production of ectopically expressed met-8 at the his-3 locus in the absence of a normal heterochromatin environment was inefficient, whereas ectopic expression of met-8 downstream of two other heterochromatin domains was efficient. In addition, our data show that the expression of mig-6 was also controlled by an upstream 4.2-kb AT-rich region similar to that of the met-8 gene, and we demonstrate that the AT-rich regions adjacent to met-8 or mig-6 are required for their peak expression. Our study indicates that met-8 and mig-6 may represent a novel type of gene, whose expression relies on the proper formation of a nearby heterochromatin region.

SUBMITTER: Yang S 

PROVIDER: S-EPMC4041435 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature

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The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region.

Yang Silu S   Li Weihua W   Qi Shaohua S   Gai Kexin K   Chen Yibo Y   Suo Jingxia J   Cao Yingqiong Y   He Yubo Y   Wang Ying Y   He Qun Q  

Nucleic acids research 20140407 10


In Neurospora crassa, the methionine synthase gene met-8 plays a key role in methionine synthesis. In this study, we found that MET-8 protein levels were compromised in several mutants defective in proper heterochromatin formation. Bioinformatics analysis revealed a 50-kb AT-rich region adjacent to the met-8 promoter. ChIP assays confirmed that trimethylated H3K9 was enriched in this region, indicating that heterochromatin may form upstream of met-8. In an H3K9R mutant strain, the output of met-  ...[more]

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