Evidence map›Paper›PMID 22569912›Full record

ReviewImmunologic research2012

Role of non-homologous end joining in V(D)J recombination.

Shruti Malu, Vidyasagar Malshetty, Dailia Francis, Patricia Cortes

Abstract readReview
PubMed Publisher
In one paragraph

Review in Immunologic research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. A dual role of Cohesin in DNA DSB repair.Nature communications · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Secrets of DNA-PKcs beyond DNA repair.NPJ precision oncology · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. The Role of DNA Repair in Genomic Instability of Multiple Myeloma.International journal of molecular sciences · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  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

4 authors.

Shruti MaluDepartment of Medicine, Immunology Institute, Mount Sinai School of Medicine, 1425 Madison Avenue, New York, NY 10029, USA.
Vidyasagar Malshetty
Dailia Francis
Patricia Cortes

Funding

Regulation of IgA class switching in the intestinal mucosaP01AI061093 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CUNNINGHAM-RUNDLES, CHARLOTTE · 2004 to 2021
$29.8M
Regulation of V(D)J recombination by Rag2 C terminusR01AI070880 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CORTES, PATRICIA · 2010 to 2014
$1.6M
Mechanism and regulation of V(D)J repairR01AI080755 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CORTES, PATRICIA · 2009 to 2013
$1.6M
Artemis: Biochemical ,structural and functional analysisR01AI070532 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CORTES, PATRICIA · 2009 to 2010
$834k
Artemis: Biochemical, structural and functional analysisR56AI070532 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CORTES, PATRICIA · 2007 to 2007
$424k
NIAID NIH HHS P01 AI061093NIAID NIH HHS R01 AI070532NIAID NIH HHS R01 AI070880NIAID NIH HHS R01 AI080755NIAID NIH HHS R56AI070532-01A1
6 · The paper itself

Abstract

The pathway of V(D)J recombination was discovered almost three decades ago. Yet it continues to baffle scientists because of its inherent complexity and the multiple layers of regulation that are required to efficiently generate a diverse repertoire of T and B cells. The non-homologous end-joining (NHEJ) DNA repair pathway is an integral part of the V(D)J reaction, and its numerous players perform critical functions in generating this vast diversity, while ensuring genomic stability. In this review, we summarize the efforts of a number of laboratories including ours in providing the mechanisms of V(D)J regulation with a focus on the NHEJ pathway. This involves discovering new players, unraveling unknown roles for known components, and understanding how deregulation of these pathways contributes to generation of primary immunodeficiencies. A long-standing interest of our laboratory has been to elucidate various mechanisms that control RAG activity. Our recent work has focused on understanding the multiple protein-protein interactions and protein-DNA interactions during V(D)J recombination, which allow efficient and regulated generation of the antigen receptors. Exploring how deregulation of this process contributes to immunodeficiencies also continues to be an important area of research for our group.

Indexed as

DNA End-Joining RepairV(D)J RecombinationAnimalsHumansModels, MolecularSevere Combined Immunodeficiency

Identifiers

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.