Evidence map›Paper›PMID 18293007›Full record

ArticleChromosoma2008

Cytological analysis of MRE11 protein during early meiotic prophase I in Arabidopsis and tomato.

Leslie D Lohmiller, Arnaud De Muyt, Brittany Howard, Hildo H Offenberg, Christa Heyting, Mathilde Grelon, Lorinda K Anderson

Abstract read
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In one paragraph

Article in Chromosoma, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Identification and Analysis ofFrontiers in plant science · 2016
    Article
  6. Combined fluorescent and electron microscopic imaging unveils the specific properties of two classes of meiotic crossovers.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  7. Article
  8. Article
  9. Cohesin proteins load sequentially during prophase I in tomato primary microsporocytes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2011
    Article
  10. PHS1 regulates meiotic recombination and homologous chromosome pairing by controlling the transport of RAD50 to the nucleus.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  11. Article
  12. 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

7 authors at 3 institutions in 3 countries.

Leslie D LohmillerDepartment of Biology, Colorado State University, Fort Collins, CO 80523, USA.
Arnaud De Muyt
Brittany Howard
Hildo H Offenberg
Christa Heyting
Mathilde Grelon
Lorinda K Anderson
Colorado State University · USAgroParisTech · FRWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early recombination nodules (ENs) are multiprotein complexes that are thought to be involved in synapsis and recombination, but little is known about their components or how they may be involved in these events. In this study, we describe the cytological behavior of a possible EN component, MRE11, a protein that is important for the repair of the numerous, programmed deoxyribonucleic acid double-strand breaks (DSBs) that occur early in the meiotic prophase. By immunofluorescence, many MRE11 foci were associated with chromosomal axes during early prophase I in both wild-type Arabidopsis and tomato primary microsporocytes. Similar patterns of MRE11 foci were observed in two Arabidopsis mutants (Atspo11-1 and Atprd1) that are defective in DSB formation and synapsis. In tomato chromosomes, MRE11 foci were more common in distal euchromatin than in proximal heterochromatin, consistent with known EN patterns. However, electron microscopic immunogold localization demonstrated that only about 10% of ENs were labeled, and most MRE11 label was associated with synaptonemal complex components. Thus, in plants, MRE11 foci are not dependent on DSB formation, and most MRE11 foci do not correspond to ENs. More generally, our results show that the simple presence of large numbers of fluorescent foci associated with synapsing chromosomes is insufficient evidence to equate these foci with ENs.

Indexed as

Meiotic Prophase IArabidopsisArabidopsis ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneDeoxyribonuclease IDNA-Binding ProteinsFluorescent Antibody TechniqueMRE11 Homologue ProteinMutationProtein TransportRecombination, GeneticRepetitive Sequences, Nucleic AcidSolanum lycopersicumStructural Maintenance of Chromosome Protein 1Synaptonemal ComplexArabidopsis ProteinsASY1 protein, ArabidopsisCell Cycle ProteinsChromosomal Proteins, Non-HistoneDeoxyribonuclease IDNA-Binding ProteinsMRE11 Homologue ProteinMre11 protein, ArabidopsisStructural Maintenance of Chromosome Protein 1

Identifiers

PMID18293007
OpenAlexW2146827361

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.