Evidence map›Paper›PMID 35608297›Full record

ArticlePlant physiology2022

An Arabidopsis pre-RNA processing8a (prp8a) missense allele restores splicing of a subset of mis-spliced mRNAs.

Roxanna J Llinas, Jia Qi Xiong, Natalie M Clark, Sarah E Burkhart, Bonnie Bartel

Open access · bronzeAbstract read
In one paragraph

Article in Plant physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 8 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

5 authors at 2 institutions in 1 country.

Roxanna J LlinasDepartment of Biosciences, Rice University, Houston, Texas 77005, USA.ORCID 0000-0002-6479-5426
Jia Qi XiongDepartment of Biosciences, Rice University, Houston, Texas 77005, USA.ORCID 0000-0001-5176-2038
Natalie M ClarkDepartment of Plant Pathology and Microbiology, Iowa State University, Ames, Iowa 50011, USA.ORCID 0000-0003-0988-321X
Sarah E BurkhartDepartment of Biosciences, Rice University, Houston, Texas 77005, USA.ORCID 0000-0003-3846-9149
Bonnie BartelDepartment of Biosciences, Rice University, Houston, Texas 77005, USA.ORCID 0000-0002-6367-346X
Rice University · USIowa State University · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Peroxisome biogenesis, dynamics, and degradation - Administrative SupplementR35GM130338 · NIGMS · RICE UNIVERSITY · PI Bonnie Bartel · 2019 to 2026
$3.3M
Using suppressor analysis to elucidate peroxisome biogenesis and peroxin functionF31GM125367 · NIGMS · RICE UNIVERSITY · PI LLINAS, ROXANNA · 2017 to 2020
$149k
NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842NIGMS NIH HHS F31 GM125367NIGMS NIH HHS R35 GM130338
6 · The paper itself

Abstract

Eukaryotic precursor mRNAs often harbor noncoding introns that must be removed prior to translation. Accurate splicing of precursor messenger RNA depends on placement and assembly of small nuclear ribonucleoprotein (snRNP) sub-complexes of the spliceosome. Yeast (Saccharomyces cerevisiae) studies established a role in splice-site selection for PRE-RNA PROCESSING8 (PRP8), a conserved spliceosome scaffolding protein of the U5 snRNP. However, analogous splice-site selection studies in multicellular eukaryotes are lacking. Such studies are crucial for a comprehensive understanding of alternative splicing, which is extensive in plants and animals but limited in yeast. In this work, we describe an Arabidopsis (Arabidopsis thaliana) prp8a mutant that modulates splice-site selection. We isolated prp8a-14 from a screen for suppressors of pex14-6, which carries a splice-site mutation in the PEROXIN14 (PEX14) peroxisome biogenesis gene. To elucidate Arabidopsis PRP8A function in spliceosome fidelity, we combined prp8a-14 with various pex14 splice-site mutations and monitored the double mutants for physiological and molecular consequences of dysfunctional and functional peroxisomes that correspond to impaired and recovered splicing, respectively. prp8a-14 restored splicing and PEX14 function to alleles with mutations in the exonic guanine of the 5'-splice site but did not restore splicing or function to alleles with mutations in the intronic guanine of 5'- or 3'-splice sites. We used RNA-seq to reveal the systemic impact of prp8a-14 and found hundreds of differentially spliced transcripts and thousands of transcripts with significantly altered levels. Among differentially spliced transcripts, prp8a-14 significantly altered 5'- and 3'-splice-site utilization to favor sites resulting in shorter introns. This study provides a genetic platform for probing splicing in plants and hints at a role for plant PRP8 in splice-site selection.

Indexed as

ArabidopsisSaccharomyces cerevisiae ProteinsAllelesAnimalsGuanineIntronsMutationRibonucleoprotein, U4-U6 Small NuclearRNARNA, MessengerRNA PrecursorsRNA SplicingSaccharomyces cerevisiaeGuanineRibonucleoprotein, U4-U6 Small NuclearRNARNA, MessengerRNA PrecursorsSaccharomyces cerevisiae Proteins

Identifiers

PMID35608297
PMCPMC9342983
OpenAlexW4281634027

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.