Literature DB >> 8543061

Human ClpP protease: cDNA sequence, tissue-specific expression and chromosomal assignment of the gene.

P Bross1, B S Andresen, I Knudsen, T A Kruse, N Gregersen.   

Abstract

We identified three overlapping human expressed sequence tags with significant homology to the E. coli ClpP amino sequence by screening the EMBL nucleotide database. With this sequence information we applied 5' and 3'-rapid amplification of cDNA ends (RACE) to amplify and sequence human clpP cDNA in two overlapping fragments. The open reading frame encodes a 277 amino acid long precursor polypeptide. Two ClpP specific motifs surrounding the active site residues are present and extensive homology to ClpP's from other organisms was observed. Northern blotting showed high relative expression levels of clpP mRNA in skeletal muscle, intermediate levels in heart, liver and pancreas, and low levels in brain, placenta, lung and kidney. By analysis of human/rodent cell hybrids the human clpP gene was assigned to chromosome 19.

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Year:  1995        PMID: 8543061     DOI: 10.1016/0014-5793(95)01353-9

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  12 in total

1.  Rapid degradation of the presequence of the f1beta precursor of the ATP synthase inside mitochondria.

Authors:  A Ståhl; P F Pavlov; C Szigyarto; E Glaser
Journal:  Biochem J       Date:  2000-08-01       Impact factor: 3.857

2.  Turnover of matrix proteins in mammalian mitochondria.

Authors:  Walter Huth; Stefan Rolle; Ilona Wunderlich
Journal:  Biochem J       Date:  2002-05-15       Impact factor: 3.857

Review 3.  The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders.

Authors:  N Gregersen; P Bross; B S Andrese; C B Pedersen; T J Corydon; L Bolund
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

4.  Down-regulation of the mitochondrial matrix peptidase ClpP in muscle cells causes mitochondrial dysfunction and decreases cell proliferation.

Authors:  Sathyaseelan S Deepa; Shylesh Bhaskaran; Rojina Ranjit; Rizwan Qaisar; Binoj C Nair; Yuhong Liu; Michael E Walsh; Wilson C Fok; Holly Van Remmen
Journal:  Free Radic Biol Med       Date:  2015-12-23       Impact factor: 7.376

Review 5.  Regulated protein degradation in mitochondria.

Authors:  T Langer; W Neupert
Journal:  Experientia       Date:  1996-12-15

6.  Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease.

Authors:  Emma M Jenkinson; Atteeq U Rehman; Tom Walsh; Jill Clayton-Smith; Kwanghyuk Lee; Robert J Morell; Meghan C Drummond; Shaheen N Khan; Muhammad Asif Naeem; Bushra Rauf; Neil Billington; Julie M Schultz; Jill E Urquhart; Ming K Lee; Andrew Berry; Neil A Hanley; Sarju Mehta; Deirdre Cilliers; Peter E Clayton; Helen Kingston; Miriam J Smith; Thomas T Warner; Graeme C Black; Dorothy Trump; Julian R E Davis; Wasim Ahmad; Suzanne M Leal; Sheikh Riazuddin; Mary-Claire King; Thomas B Friedman; William G Newman
Journal:  Am J Hum Genet       Date:  2013-03-28       Impact factor: 11.025

7.  A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization.

Authors:  T J Corydon; P Bross; H U Holst; S Neve; K Kristiansen; N Gregersen; L Bolund
Journal:  Biochem J       Date:  1998-04-01       Impact factor: 3.857

Review 8.  Reprogramming of the Caseinolytic Protease by ADEP Antibiotics: Molecular Mechanism, Cellular Consequences, Therapeutic Potential.

Authors:  Heike Brötz-Oesterhelt; Andreas Vorbach
Journal:  Front Mol Biosci       Date:  2021-05-13

9.  Perrault syndrome type 3 caused by diverse molecular defects in CLPP.

Authors:  Erica J Brodie; Hanmiao Zhan; Tamanna Saiyed; Kaye N Truscott; David A Dougan
Journal:  Sci Rep       Date:  2018-08-27       Impact factor: 4.379

10.  Imipridone Anticancer Compounds Ectopically Activate the ClpP Protease and Represent a New Scaffold for Antibiotic Development.

Authors:  Samuel Jacques; Almer M van der Sloot; Caroline C Huard; Jasmin Coulombe-Huntington; Sarah Tsao; Sylvain Tollis; Thierry Bertomeu; Elizabeth J Culp; Daniel Pallant; Michael A Cook; Eric Bonneil; Pierre Thibault; Gerard D Wright; Mike Tyers
Journal:  Genetics       Date:  2020-02-24       Impact factor: 4.562

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