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Series GSE222905 Query DataSets for GSE222905
Status Public on Jan 19, 2023
Title DNMT3A-coordinated splicing governs the stem state switch toward differentiation in embryonic and hematopoietic stem cells [RNA-seq]
Organisms Homo sapiens; Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Upon stimulation by extrinsic stimuli, stem cells initiate a program that enables differentiation or self-renewal. Disruption of the stem-state exit has catastrophic consequences for embryogenesis and can lead to cancer. While some elements of this stem-state switch are known, major regulatory mechanisms remain unclear. Here, we show this switch involves a global increase in splicing efficiency coordinated by DNMT3A, an enzyme typically involved in DNA methylation. Proper activation of murine and human embryonic and hematopoietic stem cells depends on mRNA processing influenced by DNMT3A in response to stimuli. DNMT3A coordinates splicing through recruitment of the core spliceosome protein SF3B1 to RNA polymerase and mRNA. Importantly, the DNA methylation function of DNMT3A is not required and loss of DNMT3A leads to impaired splicing during stem cell turnover. Finally, we identify the spliceosome as a potential therapeutic target in DNMT3A-mutated leukemias. Together, our results reveal a modality through which DNMT3A and the spliceosome govern exit from the stem-state towards differentiation. 
 
Overall design mRNA sequencing (RNA-seq) of DNMT3A WT and KO cells in mouse and human HSCs and ESCs
Total RNA was isolated from mouse HSCs and human HSPCs using PicoPure RNA isolation kit (KIT0204). RNA from mESC and hESC was isolated using the Qiagen mini kit. Quality of isolated RNA was verified with Nanodrop and tapestation prior to library preparation. 500-750ng of total RNA was used was used as input for the Illumina TruSeq Stranded mRNA LT Prep Kit (20020594). Libraries were made following Illumina’s recommended protocol. Amplified libraries were purified and quantified using the KAPA quantification kit. RNA sequencing libraries were sequenced on an Illumina NextSeq 500 instrument (paired-end).
 
Contributor(s) Ramabadran R, Reyes J, Wang J
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Submission date Jan 14, 2023
Last update date Jan 19, 2023
Contact name Margaret Goodell
Organization name Baylor College of Medicine
Street address One Baylor Plaza, N1030
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platforms (2)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (16)
GSM6935043 hematopoietic stem cells, DNMT3AWT, rep1 [mHSC_DNMT3AWT_1]
GSM6935044 hematopoietic stem cells, DNMT3AWT, rep2 [mHSC_DNMT3AWT_2]
GSM6935045 hematopoietic stem cells, DNMT3AKO, rep1 [mHSC_DNMT3AKO_1]
This SubSeries is part of SuperSeries:
GSE222906 DNMT3A-coordinated splicing governs the stem state switch toward differentiation in embryonic and hematopoietic stem cells.
Relations
BioProject PRJNA923814

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE222905_hESC.txt.gz 3.0 Mb (ftp)(http) TXT
GSE222905_hHSC.txt.gz 2.8 Mb (ftp)(http) TXT
GSE222905_mESC.txt.gz 1.4 Mb (ftp)(http) TXT
GSE222905_mHSC.txt.gz 1.8 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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