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N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [MeRIP-seq]

ABSTRACT: N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [MeRIP-seq]

PROVIDER: PRJNA415689 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR6211494.fastq.gz	Fastqsanger.gz
	SRR6211494_1.fastq.gz	Fastqsanger.gz
	SRR6211494_2.fastq.gz	Fastqsanger.gz
	SRR6211495_1.fastq.gz	Fastqsanger.gz
	SRR6211495_2.fastq.gz	Fastqsanger.gz

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N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis

Project description:N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis

| PRJNA415638 | ENA

N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [crispr]

Project description:N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [crispr]

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N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [CUT&RUN]

Project description:N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [CUT&RUN]

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N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis[Ribosome Profiling]

Project description:N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis[Ribosome Profiling]

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N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [MeRIP-seq]

Project description:Many of the regulatory features governing erythrocyte specification, maturation, and associated disorders remain enigmatic. To identify new regulators of erythropoiesis, we performed a functional genomic screen for genes affecting expression of the erythroid marker CD235a/GYPA. Among validating hits were genes coding for the N6-methyladenosine (m6A) mRNA methyltransferase (MTase) complex, including, METTL14, METTL3, and WTAP. We found that m6A MTase activity promotes erythroid gene expression programs through selective translation of ~300 m6A marked mRNAs, including those coding for SETD histone methyltransferases, ribosomal components, and polyA RNA binding proteins, and novel genes. Remarkably, loss of m6A marks resulted in dramatic loss of H3K4me3 marks across key erythroid-specific KLF1 transcriptional targets (e.g., Heme biosynthesis genes). Further, each m6A MTase subunit and a subset of their mRNAs targets are required for human erythroid specification in primary bone-marrow derived progenitors. Thus, m6A mRNA marks promote the translation of a network of genes required for human erythropoiesis.

2019-08-12 | GSE106122 | GEO

N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [crispr]

2019-08-12 | GSE105779 | GEO

N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [CUT&RUN]

2019-08-12 | GSE117314 | GEO

N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis[Ribosome Profiling]

2019-08-12 | GSE105782 | GEO

N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [RNA-Seq]

2019-08-12 | GSE95372 | GEO

N<sup>6</sup>-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis.

Project description:Many of the regulatory features governing erythrocyte specification, maturation, and associated disorders remain enigmatic. To identify new regulators of erythropoiesis, we utilize a functional genomic screen for genes affecting expression of the erythroid marker CD235a/GYPA. Among validating hits are genes coding for the N6-methyladenosine (m6A) mRNA methyltransferase (MTase) complex, including, METTL14, METTL3, and WTAP. We demonstrate that m6A MTase activity promotes erythroid gene expression programs through selective translation of ~300?m6A marked mRNAs, including those coding for SETD histone methyltransferases, ribosomal components, and polyA RNA binding proteins. Remarkably, loss of m6A marks results in dramatic loss of H3K4me3 marks across key erythroid-specific KLF1 transcriptional targets (e.g., Heme biosynthesis genes). Further, each m6A MTase subunit and a subset of their mRNAs targets are required for human erythroid specification in primary bone-marrow derived progenitors. Thus, m6A mRNA marks promote the translation of a network of genes required for human erythropoiesis.

| S-EPMC6787028 | biostudies-literature

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