Evidence map›Paper›PMID 16180137›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2005

Identification of mutations from phenotype-driven ENU mutagenesis in mouse chromosome 7.

Cymbeline T Culiat, Mitchell L Klebig, Zhaowei Liu, Heidi Monroe, Beverly Stanford, Jayashree Desai, Samvit Tandan, Lori Hughes, Marilyn K Kerley, Donald A Carpenter and 3 more

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    Review
  5. 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

13 authors at 3 institutions in 1 country.

Cymbeline T CuliatLife Sciences Division, Oak Ridge National Laboratory, Bethel Valley Road, P.O. Box 2008, Oak Ridge, Tennessee, 37831-6445, USA. culiatct@ornl.gov
Mitchell L Klebig
Zhaowei Liu
Heidi Monroe
Beverly Stanford
Jayashree Desai
Samvit Tandan
Lori Hughes
Marilyn K Kerley
Donald A Carpenter
Dabney K Johnson
Eugene M Rinchik
Qingbo Li
Oak Ridge National Laboratory · USSpectrum Research (United States) · USUniversity of Tennessee at Knoxville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have used the new high-throughput mutation-scanning technique temperature-gradient capillary electrophoresis (TGCE) for the identification of point mutations induced by N-ethyl-N-nitrosourea (ENU) in the mouse genome. TGCE detects the presence of heteroduplex molecules formed between a wild-type gene segment and the corresponding homologous segment containing an induced mutation or a naturally occurring single nucleotide polymorphism (SNP). Partially denatured heteroduplex molecules are resolved from homoduplexes by virtue of their differential mobilities during capillary electrophoresis conducted in a finely controlled temperature gradient. Simultaneous heteroduplex analysis of 96 amplicons ranging from 150 to 600 bp in size is achieved in approximately 45 min without the need for predetermining the melting profile of each fragment. Initially, we exploited known mouse mutations to develop TGCE protocols for analyzing unpurified PCR samples amplified from crude tail-DNA preparations. TGCE was then applied to the rapid identification of three new ENU-induced mutations recovered from regional mutagenesis screens of a segment of mouse Chromosome 7. Enzyme assays and quantitative reverse transcription-PCR (qRT-PCR) methods validated these new mutations. Our data demonstrate that rapid mutation scanning with TGCE, followed by sequence verification only of detected positives, is an efficient approach to the identification of point mutations in the mouse genome.

Indexed as

DNA Mutational AnalysisAnimalsBase SequenceChromatography, High Pressure LiquidChromosomes, MammalianElectrophoresis, CapillaryEthylnitrosoureaHeteroduplex AnalysisIsoenzymesL-Lactate DehydrogenaseMiceMice, Inbred BALB CMutagenesisOxygenasesPhenotypePoint MutationEthylnitrosoureafatty acid alpha-hydroperoxylaseIsoenzymeslactate dehydrogenase 1L-Lactate DehydrogenaseOxygenasesSaa3 protein, mouseSerum Amyloid A Protein

Identifiers

PMID16180137
OpenAlexW1995648270

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.