Evidence map›Paper›PMID 12432495›Full record

ArticleAmerican journal of human genetics2002

Male mouse recombination maps for each autosome identified by chromosome painting.

Lutz Froenicke, Lorinda K Anderson, Johannes Wienberg, Terry Ashley

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

104 citing papers in PubMed, 201 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Dissecting the Meiotic Recombination Patterns in aInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Meiotic Crossover Patterning.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

44 more citing papers are in PubMed but not listed here.

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

4 authors at 4 institutions in 2 countries.

Lutz FroenickeComparative Molecular Cytogenetics Section, Genetics Branch, National Cancer Institute, Frederick, MD, USA.
Lorinda K Anderson
Johannes Wienberg
Terry Ashley
Colorado State University · USInstitute of Human Genetics · PLNational Cancer Institute · USYale University · US

Funding

MECHANISMS OF MAMMALIAN MEIOTIC SYNAPSISR01GM055300 · NIGMS · YALE UNIVERSITY · PI ASHLEY, TERRY · 1997 to 2000
$221k
NIGMS NIH HHS R01-GM55300
6 · The paper itself

Abstract

Linkage maps constructed from genetic analysis of gene order and crossover frequency provide few clues to the basis of genomewide distribution of meiotic recombination, such as chromosome structure, that influences meiotic recombination. To bridge this gap, we have generated the first cytological recombination map that identifies individual autosomes in the male mouse. We prepared meiotic chromosome (synaptonemal complex [SC]) spreads from 110 mouse spermatocytes, identified each autosome by multicolor fluorescence in situ hybridization of chromosome-specific DNA libraries, and mapped >2,000 sites of recombination along individual autosomes, using immunolocalization of MLH1, a mismatch repair protein that marks crossover sites. We show that SC length is strongly correlated with crossover frequency and distribution. Although the length of most SCs corresponds to that predicted from their mitotic chromosome length rank, several SCs are longer or shorter than expected, with corresponding increases and decreases in MLH1 frequency. Although all bivalents share certain general recombination features, such as few crossovers near the centromeres and a high rate of distal recombination, individual bivalents have unique patterns of crossover distribution along their length. In addition to SC length, other, as-yet-unidentified, factors influence crossover distribution leading to hot regions on individual chromosomes, with recombination frequencies as much as six times higher than average, as well as cold spots with no recombination. By reprobing the SC spreads with genetically mapped BACs, we demonstrate a robust strategy for integrating genetic linkage and physical contig maps with mitotic and meiotic chromosome structure.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarrier ProteinsChromosome PaintingChromosomes, Artificial, BacterialChromosomes, MammalianCrossing Over, GeneticMaleMeiosisMiceMice, Inbred C57BLMitosisMutL Protein Homolog 1Neoplasm ProteinsNuclear ProteinsPhysical Chromosome MappingAdaptor Proteins, Signal TransducingCarrier ProteinsMlh1 protein, mouseMutL Protein Homolog 1Neoplasm ProteinsNuclear Proteins

Identifiers

PMID12432495
PMCPMC517487
OpenAlexW2170776134

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.