Evidence map›Paper›PMID 16581784›Full record

ArticleMolecular and cellular biology2006

Transcription of a donor enhances its use during double-strand break-induced gene conversion in human cells.

Ezra Schildkraut, Cheryl A Miller, Jac A Nickoloff

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  6. Article
  7. Transcription as a source of genome instability.Nature reviews. Genetics · 2012
    Review
  8. 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

3 authors at 1 institution in 1 country.

Ezra SchildkrautDepartment of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA. jnickoloff@salud.unm.edu
Cheryl A Miller
Jac A Nickoloff
University of New Mexico · US

Funding

MAMMILIAN DOUBLE STRAND BREAK AND RECOMBINATIONAL REPAIRR01CA077693 · NCI · UNIVERSITY OF NEW MEXICO · PI OSLEY, MARY ANN · 1999 to 2008
$2.4M
NCI NIH HHS CA 77693NCI NIH HHS R01 CA077693
6 · The paper itself

Abstract

Homologous recombination (HR) mediates accurate repair of double-strand breaks (DSBs) but carries the risk of large-scale genetic change, including loss of heterozygosity, deletions, inversions, and translocations. Nearly one-third of the human genome consists of repetitive sequences, and DSB repair by HR often requires choices among several homologous repair templates, including homologous chromosomes, sister chromatids, and linked or unlinked repeats. Donor preference during DSB-induced gene conversion was analyzed by using several HR substrates with three copies of neo targeted to a human chromosome. Repair of I-SceI nuclease-induced DSBs in one neo (the recipient) required a choice between two donor neo genes. When both donors were downstream, there was no significant bias for proximal or distal donors. When donors flanked the recipient, we observed a marked (85%) preference for the downstream donor. Reversing the HR substrate in the chromosome eliminated this preference, indicating that donor choice is influenced by factors extrinsic to the HR substrate. Prior indirect evidence suggested that transcription might increase donor use. We tested this question directly and found that increased transcription of a donor enhances its use during gene conversion. A preference for transcribed donors would minimize the use of nontranscribed (i.e., pseudogene) templates during repair and thus help maintain genome stability.

Indexed as

DNA DamageGene ConversionRecombination, GeneticTranscription, GeneticAllelesCell LineDeoxyribonucleases, Type II Site-SpecificDexamethasoneGene DeletionHumansSaccharomyces cerevisiae ProteinsSubstrate SpecificityDeoxyribonucleases, Type II Site-SpecificDexamethasoneSaccharomyces cerevisiae ProteinsSCEI protein, S cerevisiae

Identifiers

PMID16581784
PMCPMC1446947
OpenAlexW2103924273

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.