Evidence map›Paper›PMID 25402171›Full record

ArticlePloS one2014

Arabidopsis mTERF15 is required for mitochondrial nad2 intron 3 splicing and functional complex I activity.

Ya-Wen Hsu, Huei-Jing Wang, Ming-Hsiun Hsieh, Hsu-Liang Hsieh, Guang-Yuh Jauh

Open access · goldAbstract 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 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

60 citing papers in PubMed, 116 citations in OpenAlex.

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  20. The ChloroplastCells · 2021
    Review
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.

Ya-Wen HsuInstitute of Plant Biology, National Taiwan University, Taipei, 116, Taiwan, ROC; Institute of Plant and Microbial Biology, Academia Sinica, Nankang, Taipei, 11529, Taiwan, ROC.
Huei-Jing WangInstitute of Plant and Microbial Biology, Academia Sinica, Nankang, Taipei, 11529, Taiwan, ROC.
Ming-Hsiun HsiehInstitute of Plant and Microbial Biology, Academia Sinica, Nankang, Taipei, 11529, Taiwan, ROC.
Hsu-Liang HsiehInstitute of Plant Biology, National Taiwan University, Taipei, 116, Taiwan, ROC.
Guang-Yuh JauhInstitute of Plant and Microbial Biology, Academia Sinica, Nankang, Taipei, 11529, Taiwan, ROC; Biotechnology Center, National Chung-Hsing University, Taichung, 402, Taiwan, ROC.
Institute of Plant and Microbial Biology, Academia Sinica · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria play a pivotal role in most eukaryotic cells, as they are responsible for the generation of energy and diverse metabolic intermediates for many cellular events. During endosymbiosis, approximately 99% of the genes encoded by the mitochondrial genome were transferred into the host nucleus, and mitochondria import more than 1000 nuclear-encoded proteins from the cytosol to maintain structural integrity and fundamental functions, including DNA replication, mRNA transcription and RNA metabolism of dozens of mitochondrial genes. In metazoans, a family of nuclear-encoded proteins called the mitochondrial transcription termination factors (mTERFs) regulates mitochondrial transcription, including transcriptional termination and initiation, via their DNA-binding activities, and the dysfunction of individual mTERF members causes severe developmental defects. Arabidopsis thaliana and Oryza sativa contain 35 and 48 mTERFs, respectively, but the biological functions of only a few of these proteins have been explored. Here, we investigated the biological role and molecular mechanism of Arabidopsis mTERF15 in plant organelle metabolism using molecular genetics, cytological and biochemical approaches. The null homozygous T-DNA mutant of mTERF15, mterf15, was found to result in substantial retardation of both vegetative and reproductive development, which was fully complemented by the wild-type genomic sequence. Surprisingly, mitochondria-localized mTERF15 lacks obvious DNA-binding activity but processes mitochondrial nad2 intron 3 splicing through its RNA-binding ability. Impairment of this splicing event not only disrupted mitochondrial structure but also abolished the activity of mitochondrial respiratory chain complex I. These effects are in agreement with the severe phenotype of the mterf15 homozygous mutant. Our study suggests that Arabidopsis mTERF15 functions as a splicing factor for nad2 intron 3 splicing in mitochondria, which is essential for normal plant growth and development.

Indexed as

IntronsRNA SplicingArabidopsisArabidopsis ProteinsElectron Transport Complex IMembrane Potential, MitochondrialMitochondriaMitochondrial TurnoverMutationPhenotypeProtein TransportArabidopsis ProteinsElectron Transport Complex I

Identifiers

PMID25402171
PMCPMC4234379
OpenAlexW1966543339

What OpenQuestion holds

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LicenceCC BY
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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.