Evidence map›Paper›PMID 25457772›Full record

ArticleDNA repair2014

Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding.

Kishore K Chiruvella, Brian M Renard, Shanda R Birkeland, Sham Sunder, Zhuobin Liang, Thomas E Wilson

Open access · greenAbstract read
In one paragraph

Article in DNA repair, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Consider the workhorse: Nonhomologous end-joining in budding yeast.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2016
    Review
  3. 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

6 authors at 1 institution in 1 country.

Kishore K ChiruvellaDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Brian M RenardDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Shanda R BirkelandDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Sham SunderDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Zhuobin LiangDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Thomas E WilsonDepartments of Pathology and Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: wilsonte@umich.edu.
University of Michigan · US

Funding

Systematic Genetic Analysis of Yeast NHEJR01CA102563 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILSON, THOMAS EDWARD · 2004 to 2014
$2.4M
Systematic Genetic Analysis of Yeast NHEJR56CA102563 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILSON, THOMAS EDWARD · 2009 to 2009
$242k
NCI NIH HHS CA102563NCI NIH HHS R01 CA102563NCI NIH HHS R56 CA102563
6 · The paper itself

Abstract

LIG4/Dnl4 is the DNA ligase that (re)joins DNA double-strand breaks (DSBs) via nonhomologous end joining (NHEJ), an activity supported by binding of its tandem BRCT domains to the ligase accessory protein XRCC4/Lif1. We screened a panel of 88 distinct ligase mutants to explore the structure–function relationships of the yeast Dnl4 BRCT domains and inter-BRCT linker in NHEJ. Screen results suggested two distinct classes of BRCT mutations with differential effects on Lif1 interaction as compared to NHEJ completion. Validated constructs confirmed that D800K and GG(868:869)AA mutations, which target the Lif1 binding interface, showed a severely defective Dnl4–Lif1 interaction but a less consistent and often small decrease in NHEJ activity in some assays, as well as nearly normal levels of Dnl4 accumulation at DSBs. In contrast, mutants K742A and KTT(742:744)ATA, which target the β3-α2 region of the first BRCT domain, substantially decreased NHEJ function commensurate with a large defect in Dnl4 recruitment to DSBs, despite a comparatively greater preservation of the Lif1 interaction. Together, these separation-of-function mutants indicate that Dnl4 BRCT1 supports DSB recruitment and NHEJ in a manner distinct from Lif1 binding and reveal a complexity of Dnl4 BRCT domain functions in support of stable DSB association.

Indexed as

Protein Structure, TertiaryDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA End-Joining RepairDNA Ligase ATPDNA LigasesMutationProtein StabilitySaccharomyces cerevisiae ProteinsDNA-Binding ProteinsDNA Ligase ATPDNA LigasesDNL4 protein, S cerevisiaeLIF1 protein, S cerevisiaeLIG4 protein, humanSaccharomyces cerevisiae ProteinsXRCC4 protein, human

Identifiers

PMID25457772
PMCPMC4305023
OpenAlexW2015304465

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.