Evidence map›Paper›PMID 26588990›Full record

ArticleGenes & development2015

Context-dependent modulation of Pol II CTD phosphatase SSUP-72 regulates alternative polyadenylation in neuronal development.

Fei Chen, Yu Zhou, Yingchuan B Qi, Vishal Khivansara, Hairi Li, Sang Young Chun, John K Kim, Xiang-Dong Fu, Yishi Jin

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2015. 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
–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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Cells · 2020
    Article
  6. Review
  7. Article
  8. A protein complex regulates RNA processing of intronic heterochromatin-containing genes inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  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

9 authors at 3 institutions in 1 country.

Fei ChenNeurobiology Section, Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093, USA; Howard Hughes Medical Institute, University of California at San Diego, La Jolla, California 92093, USA;
Yu ZhouDepartment of Cellular and Molecular Medicine, School of Medicine, University of California at San Diego, La Jolla, California 92093, USA;
Yingchuan B QiNeurobiology Section, Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093, USA;
Vishal KhivansaraLife Sciences Institute, Department of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA;
Hairi LiDepartment of Cellular and Molecular Medicine, School of Medicine, University of California at San Diego, La Jolla, California 92093, USA;
Sang Young ChunDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan 48109, USA.
John K KimLife Sciences Institute, Department of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA;
Xiang-Dong FuDepartment of Cellular and Molecular Medicine, School of Medicine, University of California at San Diego, La Jolla, California 92093, USA;
Yishi JinNeurobiology Section, Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093, USA; Howard Hughes Medical Institute, University of California at San Diego, La Jolla, California 92093, USA; Department of Cellular and Molecular Medicine, School of Medicine, University of California at San Diego, La Jolla, California 92093, USA;
University of California, San Diego · USUniversity of Michigan–Ann Arbor · USHoward Hughes Medical Institute · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
FUNCTION &REGULATION OF THE HUMAN SPLICING FACTOR SC35R01GM049369 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FU, XIANG-DONG · 1993 to 2018
$7.2M
GABAERGIC NEURON DIFFERENTIATION IN C ELEGANSR01NS035546 · NINDS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JIN, YISHI · 1996 to 2016
$5.3M
Regulation of Gene Expression by microRNAs in C. elegansR01GM088565 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIM, JOHN · 2009 to 2013
$1.4M
NIGMS NIH HHS R01 GM049369NIGMS NIH HHS R01 GM088565NIGMS NIH HHS R01GM088565NIH HHS P40 OD010440NINDS NIH HHS R01 NS035546
6 · The paper itself

Abstract

Alternative polyadenylation (APA) is widespread in neuronal development and activity-mediated neural plasticity. However, the underlying molecular mechanisms are largely unknown. We used systematic genetic studies and genome-wide surveys of the transcriptional landscape to identify a context-dependent regulatory pathway controlling APA in the Caenorhabditis elegans nervous system. Loss of function in ssup-72, a Ser5 phosphatase for the RNA polymerase II (Pol II) C-terminal domain (CTD), dampens transcription termination at a strong intronic polyadenylation site (PAS) in unc-44/ankyrin yet promotes termination at the weak intronic PAS of the MAP kinase dlk-1. A nuclear protein, SYDN-1, which regulates neuronal development, antagonizes the function of SSUP-72 and several nuclear polyadenylation factors. This regulatory pathway allows the production of a neuron-specific isoform of unc-44 and an inhibitory isoform of dlk-1. Dysregulation of the unc-44 and dlk-1 mRNA isoforms in sydn-1 mutants impairs neuronal development. Deleting the intronic PAS of unc-44 results in increased pre-mRNA processing of neuronal ankyrin and suppresses sydn-1 mutants. These results reveal a mechanism by which regulation of CTD phosphorylation controls coding region APA in the nervous system.

Indexed as

AnimalsAnkyrinsCaenorhabditis elegansCaenorhabditis elegans ProteinsGene Expression Regulation, DevelopmentalMAP Kinase Kinase KinasesMutationNeuronsPhosphoprotein PhosphatasesPolyadenylationProtein BindingAnkyrinsCaenorhabditis elegans ProteinsDLK-1 protein, C elegansMAP Kinase Kinase KinasesPhosphoprotein PhosphatasesSSUP-72 phosphatase, C elegansunc-44 protein, C elegansaxon and synapse developmentC. elegansDLK-1/MAP kinasepre-mRNA 3′ end processingSYDN-1UNC-44/ankyrin

Identifiers

PMID26588990
PMCPMC4691892
OpenAlexW2287737131

What OpenQuestion holds

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LicenceCC BY-NC
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.