Evidence map›Paper›PMID 34037780›Full record

ArticleNucleic acids research2021

NSrp70 is a lymphocyte-essential splicing factor that controls thymocyte development.

Chang-Hyun Kim, Sang-Moo Park, Sun-Jae Lee, Young-Dae Kim, Se-Hwan Jang, Seon-Min Woo, Taeg-Kyu Kwon, Zee-Yong Park, Ik-Joo Chung, Hye-Ran Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Chang-Hyun KimSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.ORCID 0000-0003-1135-2258
Sang-Moo ParkSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Sun-Jae LeeSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Young-Dae KimSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Se-Hwan JangSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Seon-Min WooDepartment of Immunology, School of Medicine, Keimyung University, Daegu 42601, Korea.
Taeg-Kyu KwonDepartment of Immunology, School of Medicine, Keimyung University, Daegu 42601, Korea.
Zee-Yong ParkSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Ik-Joo ChungDepartment of Hematology-Oncology, Immunotherapy Innovation Center, Chonnam National University Medical School, Hwasun 58128, Korea.
Hye-Ran KimSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Chang-Duk JunSchool of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.ORCID 0000-0002-1372-9277
Gwangju Institute of Science and Technology · KRKeimyung University · KRChonnam National University Hwasun Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative pre-mRNA splicing is a critical step to generate multiple transcripts, thereby dramatically enlarging the proteomic diversity. Thus, a common feature of most alternative splicing factor knockout models is lethality. However, little is known about lineage-specific alternative splicing regulators in a physiological setting. Here, we report that NSrp70 is selectively expressed in developing thymocytes, highest at the double-positive (DP) stage. Global splicing and transcriptional profiling revealed that NSrp70 regulates the cell cycle and survival of thymocytes by controlling the alternative processing of various RNA splicing factors, including the oncogenic splicing factor SRSF1. A conditional-knockout of Nsrp1 (NSrp70-cKO) using CD4Cre developed severe defects in T cell maturation to single-positive thymocytes, due to insufficient T cell receptor (TCR) signaling and uncontrolled cell growth and death. Mice displayed severe peripheral lymphopenia and could not optimally control tumor growth. This study establishes a model to address the function of lymphoid-lineage-specific alternative splicing factor NSrp70 in a thymic T cell developmental pathway.

Indexed as

Alternative SplicingAnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteApoptosisCarcinogenesisCD69 AntigensCell ProliferationEmbryonic DevelopmentGenomicsHEK293 CellsHematopoiesisHumansLectins, C-TypeLymphopeniaMelanomaAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensLectins, C-TypeReceptors, Antigen, T-CellSerine-Arginine Splicing FactorsSrsf1 protein, mouse

Identifiers

PMID34037780
PMCPMC8191771
OpenAlexW3164025194

What OpenQuestion holds

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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.