Evidence map›Paper›PMID 21515825›Full record

ArticleEukaryotic cell2011

Bulk segregant analysis followed by high-throughput sequencing reveals the Neurospora cell cycle gene, ndc-1, to be allelic with the gene for ornithine decarboxylase, spe-1.

Kyle R Pomraning, Kristina M Smith, Michael Freitag

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

38 citing papers in PubMed, 66 citations in OpenAlex.

  1. The RPD3L deacetylation complex is required for facultative heterochromatin repression inProceedings of the National Academy of Sciences of the United States of America · 2024
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  6. Evolutionarily ancient BAH-PHD protein mediates Polycomb silencing.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  14. Rapid Identification of Major QTLFrontiers in microbiology · 2018
    Article
  15. Review
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  18. Review
  19. Article
  20. Cloning and Characterization ofFrontiers in plant science · 2016
    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 2 institutions in 1 country.

Kyle R PomraningDepartment of Biochemistry and Biophysics, 2011 ALS Bldg., Oregon State University, Corvallis, OR 97331-7305, USA.
Kristina M Smith
Michael Freitag
Oregon State University · USBiocom · US

Funding

Tools for Functional Analysis and Cell BiologyP01GM068087 · NIGMS · DARTMOUTH COLLEGE · PI DUNLAP, JAY C. · 2004 to 2013
$19.3M
Assembly and Maintenance of Centromeres in Filamentous FungiR01GM097637 · NIGMS · OREGON STATE UNIVERSITY · PI FREITAG, MICHAEL · 2011 to 2015
$1.3M
NIGMS NIH HHS P01 GM068087NIGMS NIH HHS R01 GM097637
6 · The paper itself

Abstract

With the advent of high-throughput DNA sequencing, it is now straightforward and inexpensive to generate high-density small nucleotide polymorphism (SNP) maps. Here we combined high-throughput sequencing with bulk segregant analysis to expedite mutation mapping. The general map location of a mutation can be identified by a single backcross to a strain enriched in SNPs compared to a standard wild-type strain. Bulk segregant analysis simultaneously increases the likelihood of determining the precise nature of the mutation. We present here a high-density SNP map between Neurospora crassa Mauriceville-1-c (FGSC2225) and OR74A (FGSC2489), the strains most typically used by Neurospora researchers to carry out mapping crosses. We further have demonstrated the utility of the Mauriceville sequence and our approach by mapping the mutation responsible for the only existing temperature-sensitive (ts) cell cycle mutation in Neurospora, nuclear division cycle-1 (ndc-1). The single T-to-C point mutation maps to the gene encoding ornithine decarboxylase (ODC), spe-1 (NCU01271), and changes a Phe to a Ser residue within a highly conserved motif next to the catalytic site of the enzyme. By growth on spermidine and complementation with a wild-type spe-1 gene, we showed that the defect in spe-1 is responsible for the ts ndc-1 mutation. Based on our results, we propose changing ndc-1 to spe-1(ndc), which reflects that this mutation results in an ODC with a specific nuclear division defect.

Indexed as

Sequence Analysis, DNAAmino Acid SequenceBase SequenceCatalytic DomainCell Cycle ProteinsCell DivisionChromosome MappingFungal ProteinsMolecular Sequence DataMutation, MissenseNeurospora crassaOrnithine DecarboxylasePhenotypePolymorphism, Single NucleotideSequence AlignmentSpermidineCell Cycle ProteinsFungal ProteinsOrnithine DecarboxylaseSpermidine

Identifiers

PMID21515825
PMCPMC3127673
OpenAlexW2096297164

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.