Evidence map›Paper›PMID 42881150›Full record

ArticleNature communications2026

LENG8 granule regulates alternative polyadenylation in mammals.

Zhicheng Wu, Chen Du, Yinming Li, Xueying Huang, Youwan Qin, Ai Zhong, Ming Rao, Fengming Liu, Hongwen Zhu, Yu Zhou and 1 more

Abstract read
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In one paragraph

Article in Nature communications, 2026. 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.

No citing paper in PubMed yet.

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.

Zhicheng Wu *Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Chen Du *College of Life Sciences, TaiKang Center for Life and Medical Sciences, RNA Institute, Wuhan University, Wuhan, China.ORCID http://orcid.org/0009-0005-0969-7136
Yinming Li *College of Life Sciences, TaiKang Center for Life and Medical Sciences, RNA Institute, Wuhan University, Wuhan, China.
Xueying HuangClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Youwan QinClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Ai ZhongCenter for Excellence in Molecular Cell Science, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, China.
Ming RaoCenter for Excellence in Molecular Cell Science, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, China.
Fengming LiuNational Center for Protein Science Shanghai, Shanghai, China.
Hongwen ZhuPrecise Genome Engineering Center, School of Life Sciences, Guangzhou University, Guangzhou, China.ORCID http://orcid.org/0000-0002-2116-4245
Yu ZhouCollege of Life Sciences, TaiKang Center for Life and Medical Sciences, RNA Institute, Wuhan University, Wuhan, China. yu.zhou@whu.edu.cn.ORCID http://orcid.org/0000-0002-2102-9377
Peng DaiClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China. daipeng@tongji.edu.cn.ORCID http://orcid.org/0009-0001-0915-3033

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32171287National Natural Science Foundation of China (National Science Foundation of China) 324B2009National Natural Science Foundation of China (National Science Foundation of China) 32525018National Natural Science Foundation of China (National Science Foundation of China) 82341023National Natural Science Foundation of China (National Science Foundation of China) 82401650Science and Technology Commission of Shanghai Municipality (Shanghai Municipal Science and Technology Commission) 228001437
6 · The paper itself

Abstract

Membraneless organelles (MLOs) participate in multiple cellular processes and layers of gene regulation. Alternative polyadenylation (APA) represents a pervasive gene regulatory mechanism that generates distinct 3' untranslated regions (UTRs) in transcripts. However, whether specific MLOs exist in mammals to regulate APA remains largely unknown. Here, we unveil a nuclear body, termed the LENG8 granule (G granule), that functions as an active hub for APA regulation. LENG8 deletion induces extensive 3'UTR lengthening in both cultured cells and male germ cells. Mechanistically, phase separation-driven LENG8 granule formation facilitates LENG8-CPSF4 interaction and promotes the subsequent assembly of the cleavage and polyadenylation (CPA) complex, thereby favoring proximal poly(A) site usage in target transcripts. We further elucidate that YTHDC1-m

Indexed as

Cytoplasmic GranulesPolyadenylation3' Untranslated RegionsAnimalsCleavage And Polyadenylation Specificity FactorHumansMaleMicePhase SeparationRNA-Binding ProteinsRNA, Messenger3' Untranslated RegionsCleavage And Polyadenylation Specificity FactorRNA-Binding ProteinsRNA, Messenger

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Registered trials

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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.