Evidence map›Paper›PMID 9419343›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Characterization of mammalian translocase of inner mitochondrial membrane (Tim44) isolated from diabetic newborn mouse kidney.

J Wada, Y S Kanwar

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 69 citations in OpenAlex.

  1. The RNA methyltransferase METTL8 installs mNature communications · 2022
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  5. Higd-1a interacts with Opa1 and is required for the morphological and functional integrity of mitochondria.Proceedings of the National Academy of Sciences of the United States of America · 2013
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  10. Review
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  12. Rap1b GTPase ameliorates glucose-induced mitochondrial dysfunction.Journal of the American Society of Nephrology : JASN · 2008
    Article
  13. Article
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  16. Hyperglycemia: its imminent effects on mammalian nephrogenesis.Pediatric nephrology (Berlin, Germany) · 2005
    Review
  17. Article
  18. Review
  19. Article
  20. Identification of a renal-specific oxido-reductase in newborn diabetic mice.Proceedings of the National Academy of Sciences of the United States of America · 2000
    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

2 authors at 1 institution in 1 country.

J WadaDepartment of Pathology, Northwestern University Medical School, 303 East Chicago Avenue, Chicago, IL 60611, USA.
Y S Kanwar
Northwestern University · US

Funding

GLOMERULAR CAPILLARY WALL: NORMAL AND PATHOLOGICR01DK028492 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KANWAR, YASHPAL S. · 1986 to 2008
$1.9M
GLOMERULAR CAPILLARY WALL--NORMAL AND PATHOLOGICR37DK028492 · NIDDK · NORTHWESTERN UNIVERSITY · PI KANWAR, YASHPAL S. · 1998 to 2003
$1.2M
NIDDK NIH HHS DK28492NIDDK NIH HHS R01 DK028492NIDDK NIH HHS R37 DK028492
6 · The paper itself

Abstract

Mammalian translocase of mitochondrial inner membrane (mTim44) was isolated during representational difference analysis of cDNA from diabetic mouse kidney. Streptozotocin-induced diabetic mouse kidney cDNA was prepared and subtracted by normal mouse kidney cDNA. By using one of the isolated cDNA fragments as a screening probe, full-length cDNA of mTim44 was isolated from lambdaZAP kidney cDNA library. At the nucleotide level, mTim44 did not exhibit significant homology with any known genes; however, at the amino acid level, it had 50% similarity and 29% identity with yeast Tim44. C-terminal FLAG epitope-tagged mTim44 fusion protein was transiently expressed in COS7 cells. By using anti-FLAG epitope M2 monoclonal antibody, mTim44 was found to have its subcellular localization associated with mitochondria. By immunoelectron microscopy, mTim44 was seen in the paracrystalline structures within the mitochondria, as well as in their cristae. Mitochondrial import assay of in vitro translated mTim44 indicated that its precursor product ( approximately 50 kDa) was imported and proteolytically processed to a mature approximately 44-kDa protein, and its translocation was inner membrane potential (DeltaPsi)-dependent. Imported mTim44 was protected from protease digestion in which outer membranes were selectively permeabilized with digitonin. The mature form of mTim44 could be recovered in the supernatant of sonicated mitochondrial membrane fraction treated with 0.1 M Na2CO3, pH 11.5. The data indicate that mTim44 is a mitochondrial inner membrane protein, one of the members of the mammalian TIM complex and up-regulated in hyperglycemic states.

Indexed as

Mitochondrial ProteinsAmino Acid SequenceAnimalsAnimals, NewbornBase SequenceCarrier ProteinsCloning, MolecularCOS CellsDiabetes Mellitus, ExperimentalDNA, ComplementaryKidneyMembrane ProteinsMiceMitochondrial Membrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsMolecular Sequence DataCarrier ProteinsDNA, ComplementaryMembrane ProteinsMitochondrial Membrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsMitochondrial ProteinsTimm44 protein, mouse

Identifiers

PMID9419343
PMCPMC18154
OpenAlexW2088512240

What OpenQuestion holds

Textmetadata
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.