Evidence map›Paper›PMID 26823015›Full record

ArticleMolecular biology of the cell2016

Regulation of mitochondrial translation of the ATP8/ATP6 mRNA by Smt1p.

Malgorzata Rak, Chen Hsien Su, Jonathan Tong Xu, Ricardo Azpiroz, Angela Mohan Singh, Alexander Tzagoloff

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Atp23p and Atp10p coordinate to regulate the assembly of yeast mitochondrial ATP synthase.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  8. Mechanisms and regulation of protein synthesis in mitochondria.Nature reviews. Molecular cell biology · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Aep3p-dependent translation of yeast mitochondrialMolecular biology of the cell · 2017
    Article
  13. 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

6 authors at 2 institutions in 1 country.

Malgorzata RakDepartment of Biological Sciences, Columbia University, New York, NY 10027.
Chen Hsien SuDepartment of Biological Sciences, Columbia University, New York, NY 10027.
Jonathan Tong XuDepartment of Biological Sciences, Columbia University, New York, NY 10027.
Ricardo AzpirozDepartment of Biological Sciences, Columbia University, New York, NY 10027.
Angela Mohan SinghDepartment of Biological Sciences, Columbia University, New York, NY 10027.
Alexander TzagoloffDepartment of Biological Sciences, Columbia University, New York, NY 10027 spud@columbia.edu.
Columbia University · USCornell University · US

Funding

ASSEMBLY OF MEMBRANES IN HEART AND YEAST MITOCHONDRIAR01HL022174 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI TZAGOLOFF, ALEXANDER A · 1985 to 2014
$3.3M
NHLBI NIH HHS HL02274NHLBI NIH HHS R01 HL022174
6 · The paper itself

Abstract

Expression of the mitochondrially encoded ATP6 and ATP8 genes is translationally regulated by F1 ATPase. We report a translational repressor (Smt1p) of the ATP6/8 mRNA that, when mutated, restores translation of the encoded Atp6p and Atp8p subunits of the ATP synthase. Heterozygous smt1 mutants fail to rescue the translation defect, indicating that the mutations are recessive. Smt1p is an intrinsic inner membrane protein, which, based on its sedimentation, has a native size twice that of the monomer. Affinity purification of tagged Smt1p followed by reverse transcription of the associated RNA and PCR amplification of the resultant cDNA with gene-specific primers demonstrated the presence in mitochondria of Smt1p-ATP8/ATP6 and Smt1p-COB mRNA complexes. These results indicate that Smt1p is likely to be involved in translational regulation of both mRNAs. Applying Occam's principle, we favor a mechanistic model in which translation of the ATP8/ATP6 bicistronic mRNA is coupled to the availability of F1 for subsequent assembly of the Atp6p and Atp8p products into the ATP synthase. The mechanism of this regulatory pathway is proposed to entail a displacement of the repressor from the translationally mute Smt1-ATP8/ATP6 complex by F1, thereby permitting the Atp22p activator to interact with and promote translation of the mRNA.

Indexed as

Gene Expression Regulation, FungalProtein BiosynthesisMethyltransferasesMitochondriaMitochondrial Proton-Translocating ATPasesProton-Translocating ATPasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsATP22 protein, S cerevisiaeATP6 protein, S cerevisiaeAtp8 protein, S cerevisiaeMethyltransferasesMitochondrial Proton-Translocating ATPasesProton-Translocating ATPasesSaccharomyces cerevisiae ProteinsSMT1 protein, S cerevisiae

Identifiers

PMID26823015
PMCPMC4791136
OpenAlexW2275981641

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.