Evidence map›Paper›PMID 24324008›Full record

ArticleMolecular and cellular biology2014

Distinct functions of human cohesin-SA1 and cohesin-SA2 in double-strand break repair.

Xiangduo Kong, Alexander R Ball, Hoang Xuan Pham, Weihua Zeng, Hsiao-Yuan Chen, John A Schmiesing, Jong-Soo Kim, Michael Berns, Kyoko Yokomori

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

60 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Cohesin mutations and chromatin changes in cancer.International journal of cancer · 2026
    Review
  4. Article
  5. Aberrant cohesin function inbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Liquid condensates: a new barrier to loop extrusion?Cellular and molecular life sciences : CMLS · 2025
    Review
  9. Review
  10. A STAG2-PAXIP1/PAGR1 axis suppresses lung tumorigenesis.The Journal of experimental medicine · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Genome control by SMC complexes.Nature reviews. Molecular cell biology · 2023
    Review
  15. Review
  16. Article
  17. Function and Evolution of the Loop Extrusion Machinery in Animals.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Article
  20. Article
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

9 authors at 1 institution in 1 country.

Xiangduo KongDepartment of Biological Chemistry, School of Medicine, University of California, Irvine, California, USA.
Alexander R Ball
Hoang Xuan Pham
Weihua Zeng
Hsiao-Yuan Chen
John A Schmiesing
Jong-Soo Kim
Michael Berns
Kyoko Yokomori
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
WOUND MIGRATION FORCE MONITORINGP41RR001192 · NCRR · UNIVERSITY OF CALIFORNIA-IRVINE · PI LYUBOVITSKY, JULIA · 1985 to 2011
$14.2M
Virtual Photonocs TechnologiesP41EB015890 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI DURKIN, ANTHONY J · 2012 to 2017
$7.0M
Molecular mechanism of DNA damage recognition in mammalsR01CA100710 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI YOKOMORI, KYOKO · 2004 to 2008
$1.2M
NCI NIH HHS CA100710NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA100710NCRR NIH HHS P41 RR001192NCRR NIH HHS RR01192NIBIB NIH HHS P41 EB015890
6 · The paper itself

Abstract

Cohesin is an essential multiprotein complex that mediates sister chromatid cohesion critical for proper segregation of chromosomes during cell division. Cohesin is also involved in DNA double-strand break (DSB) repair. In mammalian cells, cohesin is involved in both DSB repair and the damage checkpoint response, although the relationship between these two functions is unclear. Two cohesins differing by one subunit (SA1 or SA2) are present in somatic cells, but their functional specificities with regard to DNA repair remain enigmatic. We found that cohesin-SA2 is the main complex corecruited with the cohesin-loading factor NIPBL to DNA damage sites in an S/G(2)-phase-specific manner. Replacing the diverged C-terminal region of SA1 with the corresponding region of SA2 confers this activity on SA1. Depletion of SA2 but not SA1 decreased sister chromatid homologous recombination repair and affected repair pathway choice, indicating that DNA repair activity is specifically associated with cohesin recruited to damage sites. In contrast, both cohesin complexes function in the intra-S checkpoint, indicating that cell cycle-specific damage site accumulation is not a prerequisite for cohesin's intra-S checkpoint function. Our findings reveal the unique ways in which cohesin-SA1 and cohesin-SA2 participate in the DNA damage response, coordinately protecting genome integrity in human cells.

Indexed as

DNA Breaks, Double-StrandedAnimalsCell CycleCell Cycle ProteinsCell DivisionCells, CulturedChromatidsChromosomal Proteins, Non-HistoneChromosomesCohesinsDNA RepairHumansNuclear ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsNuclear Proteins

Identifiers

PMID24324008
PMCPMC3911484
OpenAlexW2021486745

What OpenQuestion holds

Textmetadata
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.