Evidence map›Paper›PMID 37162821›Full record

ArticlebioRxiv : the preprint server for biology2023

Essential roles of the ANKRD31-REC114 interaction in meiotic recombination and mouse spermatogenesis.

Jiaqi Xu, Tao Li, Coojong Kim, Michiel Boekhout, Scott Keeney

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jiaqi XuWeill Cornell Graduate School of Medical Sciences, New York, NY 10065, USA.
Tao LiMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Coojong KimMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Michiel BoekhoutMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Scott KeeneyWeill Cornell Graduate School of Medical Sciences, New York, NY 10065, USA.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Mechanism and regulation of meiotic recombinationR35GM118092 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI Scott Keeney · 2016 to 2026
$7.0M
Structural and functional principles underlying germline genome transmissionR01HD110120 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI Scott Keeney, DINSHAW J PATEL · 2022 to 2026
$2.4M
NCI NIH HHS P30 CA008748NICHD NIH HHS R01 HD110120NIGMS NIH HHS R35 GM118092
6 · The paper itself

Abstract

Meiotic DNA double-strand breaks (DSBs) initiate homologous recombination and are crucial for ensuring proper chromosome segregation. In mice, ANKRD31 recently emerged as a regulator of DSB timing, number, and location, with a particularly important role in targeting DSBs to the pseudoautosomal regions (PARs) of sex chromosomes. ANKRD31 interacts with multiple proteins, including the conserved and essential DSB-promoting factor REC114, so it was hypothesized to be a modular scaffold that "anchors" other proteins together and to meiotic chromosomes. To determine if and why the REC114 interaction is important for ANKRD31 function, we generated mice with

Indexed as

Ankrd31DNA double-strand breakshomologous recombinationMeiosisPrdm9Rec114spermatogenesisSpo11

Identifiers

PMID37162821
PMCPMC10168363
OpenAlexW4367369095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.