Evidence map›Paper›PMID 15340075›Full record

ArticleMolecular and cellular biology2004

Spontaneous mutagenesis is enhanced in Apex heterozygous mice.

Jessica Huamani, C Alex McMahan, Damon C Herbert, Robert Reddick, John R McCarrey, Mark I MacInnes, David J Chen, Christi A Walter

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

42 citing papers in PubMed, 67 citations in OpenAlex.

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  18. Review
  19. Human apurinic/apyrimidinic endonuclease 1.Antioxidants & redox signaling · 2014
    Review
  20. Uracil in duplex DNA is a substrate for the nucleotide incision repair pathway in human cells.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

8 authors at 5 institutions in 1 country.

Jessica HuamaniDepartment of Cellular & Structural Biology, The University of Texas Health Science Center at San Antonio, 78229-3900, USA.
C Alex McMahan
Damon C Herbert
Robert Reddick
John R McCarrey
Mark I MacInnes
David J Chen
Christi A Walter
The University of Texas Health Science Center at San Antonio · USLawrence Berkeley National Laboratory · USLos Alamos National Laboratory · USSouth Texas Veterans Health Care System · USThe University of Texas at San Antonio · US

Funding

ROLE OF CASPASE-2 IN OSTEOCOLAST APOPTOSIS AGE-EePENDENT OSTEOPOROSISP01AG019316 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HERMAN, BRIAN A. · 2001 to 2011
$11.3M
Germ Cell AgingR01AG021163 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WALTER, CHRISTI A · 2002 to 2007
$1.8M
Transgenic Mouse for DNA Damage Sensing and SignalingR01CA086936 · NCI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI CHEN, DAVID J · 2002 to 2005
$1.2M
GERM CELLS--DNA REPAIR, MUTATION, &ENVIRONMENTAL AGENTSR01ES009136 · NIEHS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI WALTER, CHRISTI A · 1998 to 2001
$745k
NCI NIH HHS CA86936NCI NIH HHS R01 CA086936NIA NIH HHS AG19316NIA NIH HHS AG21163NIA NIH HHS P01 AG019316NIA NIH HHS R01 AG021163NIEHS NIH HHS ES09136NIEHS NIH HHS R01 ES009136
6 · The paper itself

Abstract

Germ line DNA directs the development of the next generation and, as such, is profoundly different from somatic cell DNA. Spermatogenic cells obtained from young adult lacI transgenic mice display a lower spontaneous mutant frequency and greater in vitro base excision repair activity than somatic cells and tissues obtained from the same mice. However, spermatogenic cells from old lacI mice display a 10-fold higher mutant frequency. This increased spontaneous mutant frequency occurs coincidentally with decreased in vitro base excision repair activity for germ cell and testicular extracts that in turn corresponds to a decreased abundance of AP endonuclease. To directly test whether a genetic diminution of AP endonuclease results in increased spontaneous mutant frequencies in spermatogenic cell types, AP endonuclease heterozygous (Apex(+/-)) knockout mice were crossed with lacI transgenic mice. Spontaneous mutant frequencies were significantly elevated (approximately twofold) for liver and spleen obtained from 3-month-old Apex(+/-) lacI(+) mice compared to frequencies from Apex(+/+) lacI(+) littermates and were additionally elevated for somatic tissues from 9-month-old mice. Spermatogenic cells from 9-month-old Apex(+/-) lacI(+) mice were significantly elevated twofold compared to levels for 9-month-old Apex(+/+) lacI(+) control mice. These data indicate that diminution of AP endonuclease has a significant effect on spontaneous mutagenesis in somatic and germ line cells.

Indexed as

MutagenesisAnimalsApoptosisBase SequenceDNADNA-(Apurinic or Apyrimidinic Site) LyaseDNA RepairGenes, ReporterHeterozygoteLiverMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicSpermatogenesisDNADNA-(Apurinic or Apyrimidinic Site) Lyase

Identifiers

PMID15340075
PMCPMC515041
OpenAlexW2094680495

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.