Evidence map›Paper›PMID 37789001›Full record

ArticleCell discovery2023

The BRCA1/BARD1 complex recognizes pre-ribosomal RNA to facilitate homologous recombination.

Duo Wu, Huang Huang, Tenglong Chen, Xiaochen Gai, Qilin Li, Chunhui Wang, Jia Yao, Yu Liu, Shang Cai, Xiaochun Yu

Open access · goldAbstract read
In one paragraph

Article in Cell discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Role of BRCA1 in glioblastoma etiology.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  9. 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

10 authors at 2 institutions in 1 country.

Duo WuWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.
Huang HuangWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.
Tenglong ChenWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.
Xiaochen GaiWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.
Qilin LiWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.ORCID http://orcid.org/0000-0002-9853-9463
Chunhui WangSchool of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.
Jia YaoThe First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Yu LiuThe First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Shang CaiSchool of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.
Xiaochun YuWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China. yuxiaochun@westlake.edu.cn.ORCID http://orcid.org/0000-0001-9840-2670
Westlake University · CNFirst Affiliated Hospital Zhejiang University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32090034National Natural Science Foundation of China (National Science Foundation of China) 81874160
6 · The paper itself

Abstract

The BRCA1/BARD1 complex plays a key role in the repair of DNA double-strand breaks (DSBs) in both somatic cells and germ cells. However, the underlying molecular mechanism by which this complex mediates DSB repair is not fully understood. Here, we examined the XY body of male germ cells, where DSBs are accumulated. We show that the recruitment of the BRCA1/BARD1 complex to the unsynapsed axis of the XY body is mediated by pre-ribosomal RNA (pre-rRNA). Similarly, the BRCA1/BARD1 complex associates with pre-rRNA in somatic cells, which not only forms nuclear foci in response to DSBs, but also targets the BRCA1/BARD1 complex to DSBs. The interactions between the BRCT domains of the BRCA1/BARD1 complex and pre-rRNA induce liquid-liquid phase separations, which may be the molecular basis of DSB-induced nuclear foci formation of the BRCA1/BARD1 complex. Moreover, cancer-associated mutations in the BRCT domains of BRCA1 and BARD1 abolish their interactions with pre-rRNA. Pre-rRNA also mediates BRCA1-dependent homologous recombination, and suppression of pre-rRNA biogenesis sensitizes cells to PARP inhibitor treatment. Collectively, this study reveals that pre-rRNA is a functional partner of the BRCA1/BARD1 complex in the DSB repair.

Identifiers

PMID37789001
PMCPMC10547766
OpenAlexW4387306011

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.