Evidence map›Paper›PMID 31753528›Full record

ReviewTrends in genetics : TIG2020

Asymmetric Histone Inheritance in Asymmetrically Dividing Stem Cells.

Matthew Wooten, Rajesh Ranjan, Xin Chen

Open access · greenAbstract readReview
In one paragraph

Review in Trends in genetics : TIG, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Vacuolar HeLife · 2024
    Article
  8. DNA polymerase delta governs parental histone transfer to DNA replication lagging strand.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Asymmetric division of stem cells and its cancer relevance.Cell regeneration (London, England) · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Mitotic drive in asymmetric epigenetic inheritance.Biochemical Society transactions · 2022
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Matthew WootenDepartment of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA.
Rajesh RanjanDepartment of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA.
Xin ChenDepartment of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: xchen32@jhu.edu.
Johns Hopkins University · US

Funding

CELLULAR AND MOLECULAR BIOLOGYT32GM007231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 1985 to 2020
$18.4M
Study epigenetic inheritance during development, homeostasis and regenerationR35GM127075 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Xin Chen · 2018 to 2026
$3.2M
Molecular and cellular mechanisms underlying asymmetric histone inheritanceR01GM112008 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CHEN, XIN, XIAO, JIE · 2014 to 2017
$1.6M
Visualizing transcription factor binding and chromatin assembly on newly synthesized DNAK99GM152821 · NIGMS · FRED HUTCHINSON CANCER CENTER · PI WOOTEN, MATTHEW · 2024 to 2025
$250k
Investigating the mechanisms and generality of asymmetric histone inheritance in multiple stem cell systemsF31GM115149 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI WOOTEN, MATTHEW · 2016 to 2017
$88k
NIGMS NIH HHS F31 GM115149NIGMS NIH HHS K99 GM152821NIGMS NIH HHS R01 GM112008NIGMS NIH HHS R35 GM127075NIGMS NIH HHS T32 GM007231
6 · The paper itself

Abstract

Epigenetic mechanisms play essential roles in determining distinct cell fates during the development of multicellular organisms. Histone proteins represent crucial epigenetic components that help specify cell identities. Previous work has demonstrated that during the asymmetric cell division of Drosophila male germline stem cells (GSCs), histones H3 and H4 are asymmetrically inherited, such that pre-existing (old) histones are segregated towards the self-renewing GSC whereas newly synthesized (new) histones are enriched towards the differentiating daughter cell. In order to further understand the molecular mechanisms underlying this striking phenomenon, two key questions must be answered: when and how old and new histones are differentially incorporated by sister chromatids, and how epigenetically distinct sister chromatids are specifically recognized and segregated. Here, we discuss recent advances in our understanding of the molecular mechanisms and cellular bases underlying these fundamental and important biological processes responsible for generating two distinct cells through one cell division.

Indexed as

AnimalsAsymmetric Cell DivisionCell DifferentiationChromosome SegregationDrosophila melanogasterDrosophila ProteinsEpigenesis, GeneticGerm CellsHistonesStem CellsDrosophila ProteinsHistonesasymmetric cell divisioncentromereepigeneticsgermlinehistonesstem cells

Identifiers

PMID31753528
PMCPMC6925335
OpenAlexW2984685659

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.