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Series GSE228292 Query DataSets for GSE228292
Status Public on May 25, 2023
Title Old and newly synthesized histones are asymmetrically distributed in Drosophila intestinal stem cell divisions
Organism Drosophila melanogaster
Experiment type Expression profiling by high throughput sequencing
Summary We report that preexisting (old) and newly synthesized (new) histones H3 and H4 are asymmetrically partitioned during the division of Drosophila intestinal stem cells (ISCs). Furthermore, the inheritance patterns of old and new H3 and H4 in postmitotic cell pairs correlate with distinct expression patterns of Delta, an important cell fate gene. To understand the biological significance of this phenomenon, we expressed a mutant H3T3A to compromise asymmetric histone inheritance. Under this condition, we observe an increase in Delta‐symmetric cell pairs and overpopulated ISC‐like, Delta‐positive cells. Single‐cell RNA‐seq assays further indicate that H3T3A expression compromises ISC differentiation. Together, our results indicate that asymmetric histone inheritance potentially contributes to establishing distinct cell identities in a somatic stem cell lineage, consistent with previous findings in Drosophila male germline stem cells.
 
Overall design H3 wild-type- or H3T3A-expressing intestines were dissected, and the tissue samples were analyzed using scRNA-seq.
 
Contributor(s) Zion EH, Ringwalt D, Rinaldi K, Kahney EW, Li Y, Chen X
Citation(s) 37255015
NIH grant(s)
Grant ID Grant title Affiliation Name
F31 DK122702 The Role of Asymmetric Histone Inheritance in Establishing Distinct Cell Identities JOHNS HOPKINS UNIVERSITY Emily Hope Zion
F31 GM122339 Investigating epigenetic inheritance patterns and mechanisms during asymmetric division of Drosophila female germline stem cells JOHNS HOPKINS UNIVERSITY Elizabeth Willa Kahney
R35 GM127075 Study epigenetic inheritance during development and across generations using multiple model JOHNS HOPKINS UNIVERSITY Xin Chen
Submission date Mar 27, 2023
Last update date Aug 29, 2023
Contact name Daniel Ringwalt
E-mail(s) dringwa1@jhu.edu
Organization name Johns Hopkins University
Department Biology
Lab Xin Chen Lab
Street address 3400N Charles St
City Baltimore
State/province MD
ZIP/Postal code 21218
Country USA
 
Platforms (1)
GPL25244 Illumina NovaSeq 6000 (Drosophila melanogaster)
Samples (2)
GSM7118431 Wild-type H3, scRNA-seq
GSM7118432 Mutant H3T3A, scRNA-seq
Relations
BioProject PRJNA949208

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Supplementary file Size Download File type/resource
GSE228292_RAW.tar 46.9 Mb (http)(custom) TAR (of MTX, TSV)
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Raw data are available in SRA
Processed data provided as supplementary file

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