Evidence map›Paper›PMID 25144378›Full record

ArticlePloS one2014

Alternative splicing of Arabidopsis IBR5 pre-mRNA generates two IBR5 isoforms with distinct and overlapping functions.

Thilanka Jayaweera, Chamindika Siriwardana, Sunethra Dharmasiri, Marcel Quint, William M Gray, Nihal Dharmasiri

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Emerging Functions of Protein Tyrosine Phosphatases in Plants.International journal of molecular sciences · 2024
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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

6 authors.

Thilanka JayaweeraDepartment of Biology, Texas State University, San Marcos, Texas, United States of America.
Chamindika SiriwardanaDepartment of Biology, Texas State University, San Marcos, Texas, United States of America; Department of Botany and Microbiology, University of Oklahoma, Norman, Oklahoma, United States of America.
Sunethra DharmasiriDepartment of Biology, Texas State University, San Marcos, Texas, United States of America.
Marcel QuintDepartment of Plant Biology, University of Minnesota, St. Paul, Minnesota, United States of America; Department of Molecular Signal Processing, Leibniz Institute of Plant Biochemistry, Halle (Saale), Germany.
William M GrayDepartment of Plant Biology, University of Minnesota, St. Paul, Minnesota, United States of America.
Nihal DharmasiriDepartment of Biology, Texas State University, San Marcos, Texas, United States of America.

Funding

Molecular mechanisms of auxin response in ArabidopsisR01GM067203 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GRAY, WILLIAM M · 2003 to 2020
$3.5M
NIGMS NIH HHS GM067203NIGMS NIH HHS R01 GM067203
6 · The paper itself

Abstract

The INDOLE-3-BUTYRIC ACID RESPONSE5 (IBR5) gene encodes a dual specificity phosphatase that regulates plant auxin responses. IBR5 has been predicted to generate two transcripts through alternative splicing, but alternative splicing of IBR5 has not been confirmed experimentally. The previously characterized ibr5-1 null mutant exhibits many auxin related defects such as auxin insensitive primary root growth, defective vascular development, short stature and reduced lateral root development. However, whether all these defects are caused by the lack of phosphatase activity is not clear. Here we describe two new auxin insensitive IBR5 alleles, ibr5-4, a catalytic site mutant, and ibr5-5, a splice site mutant. Characterization of these new mutants indicates that IBR5 is post-transcriptionally regulated to generate two transcripts, AT2G04550.1 and AT2G04550.3, and consequently two IBR5 isoforms, IBR5.1 and IBR5.3. The IBR5.1 isoform exhibits phosphatase catalytic activity that is required for both proper degradation of Aux/IAA proteins and auxin-induced gene expression. These two processes are independently regulated by IBR5.1. Comparison of new mutant alleles with ibr5-1 indicates that all three mutant alleles share many phenotypes. However, each allele also confers distinct defects implicating IBR5 isoform specific functions. Some of these functions are independent of IBR5.1 catalytic activity. Additionally, analysis of these new mutant alleles suggests that IBR5 may link ABP1 and SCF(TIR1/AFBs) auxin signaling pathways.

Indexed as

AllelesAlternative SplicingArabidopsis ProteinsDual-Specificity PhosphatasesProtein IsoformsSignal TransductionArabidopsis ProteinsDual-Specificity PhosphatasesIBR5 protein, ArabidopsisProtein Isoforms

Identifiers

PMID25144378
PMCPMC4140696

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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.