Evidence map›Paper›PMID 21750257›Full record

ArticleGenetics2011

Massive changes in genome architecture accompany the transition to self-fertility in the filamentous fungus Neurospora tetrasperma.

Christopher E Ellison, Jason E Stajich, David J Jacobson, Donald O Natvig, Alla Lapidus, Brian Foster, Andrea Aerts, Robert Riley, Erika A Lindquist, Igor V Grigoriev and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

46 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Genomic Features ofPathogens (Basel, Switzerland) · 2020
    Article
  9. Article
  10. Repeat-Induced Point Mutations Drive Divergence betweenPathogens (Basel, Switzerland) · 2019
    Article
  11. Programmed Cell Death inGenetics · 2019
    Article
  12. Article
  13. Article
  14. Evolution of recombination rates between sex chromosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  15. Article
  16. Article
  17. A-to-I RNA editing is developmentally regulated and generally adaptive for sexual reproduction inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  18. Review
  19. Article
  20. 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

11 authors at 4 institutions in 1 country.

Christopher E EllisonDepartment of Plant and Microbial Biology, University of California, Berkeley, California 94720-3102, USA. cellison@berkeley.edu
Jason E Stajich
David J Jacobson
Donald O Natvig
Alla Lapidus
Brian Foster
Andrea Aerts
Robert Riley
Erika A Lindquist
Igor V Grigoriev
John W Taylor
Joint Genome Institute · USUniversity of California, Berkeley · USUniversity of California, Riverside · USUniversity of New Mexico · US

Funding

"The development of genetics and genomics for analysis of quantitative traits"R24GM081597 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI TAYLOR, JOHN W. · 2008 to 2011
$1.4M
NIGMS NIH HHS R24 GM081597PHS HHS R01RGM081597
6 · The paper itself

Abstract

A large region of suppressed recombination surrounds the sex-determining locus of the self-fertile fungus Neurospora tetrasperma. This region encompasses nearly one-fifth of the N. tetrasperma genome and suppression of recombination is necessary for self-fertility. The similarity of the N. tetrasperma mating chromosome to plant and animal sex chromosomes and its recent origin (<5 MYA), combined with a long history of genetic and cytological research, make this fungus an ideal model for studying the evolutionary consequences of suppressed recombination. Here we compare genome sequences from two N. tetrasperma strains of opposite mating type to determine whether structural rearrangements are associated with the nonrecombining region and to examine the effect of suppressed recombination for the evolution of the genes within it. We find a series of three inversions encompassing the majority of the region of suppressed recombination and provide evidence for two different types of rearrangement mechanisms: the recently proposed mechanism of inversion via staggered single-strand breaks as well as ectopic recombination between transposable elements. In addition, we show that the N. tetrasperma mat a mating-type region appears to be accumulating deleterious substitutions at a faster rate than the other mating type (mat A) and thus may be in the early stages of degeneration.

Indexed as

Genome, FungalChromosomes, FungalCodonFertilityGene RearrangementGenes, Mating Type, FungalNeurosporaRecombination, GeneticCodon

Identifiers

PMID21750257
PMCPMC3176108
OpenAlexW2109181307

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.