Literature DB >> 11420104

The Trypanosoma brucei mitochondrial ATP synthase is developmentally regulated at the level of transcript stability.

S V Brown B1, T B Chi, N Williams.   

Abstract

The mitochondrial ATP synthase is developmentally regulated throughout the life cycle of the Trypanosoma brucei. The alpha and beta subunits of the F(1) moiety, and subunit 9 of the F(0) moiety of the T. brucei ATP synthase have been previously cloned and characterized. Here we have determined the chromosomal localization and developmental regulation of these three key subunits of the complex. Southern blot analysis indicates that all three of these genes are present as single copies in the T. brucei genome. Pulsed field gel analysis demonstrates that these genes are encoded in different chromosomes, and are thus not part of the same gene cluster. A comparison between the protein and steady state transcript levels for these subunits suggests that regulation of expression occurs predominantly posttranscriptionally. Comparison of mRNA stability for procyclic and bloodstream forms shows that the half life of the three transcripts is much shorter in bloodstream forms. The differences in transcript stability in the procyclic form for subunit 9 is greater than that for alpha and beta subunits, while the differences at the protein levels are comparable. These results suggest that there may be further posttranscriptional regulation of subunit 9.

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Year:  2001        PMID: 11420104     DOI: 10.1016/s0166-6851(01)00282-1

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  9 in total

1.  Identification of the mitochondrially encoded subunit 6 of F1FO ATPase in Trypanosoma brucei.

Authors:  Ingrid Škodová-Sveráková; Anton Horváth; Dmitri A Maslov
Journal:  Mol Biochem Parasitol       Date:  2015-08-11       Impact factor: 1.759

2.  The F1-ATP synthase complex in bloodstream stage trypanosomes has an unusual and essential function.

Authors:  Achim Schnaufer; G Desmond Clark-Walker; Alodie G Steinberg; Ken Stuart
Journal:  EMBO J       Date:  2005-11-17       Impact factor: 11.598

3.  ATP synthase is responsible for maintaining mitochondrial membrane potential in bloodstream form Trypanosoma brucei.

Authors:  Silvia V Brown; Paul Hosking; Jinlei Li; Noreen Williams
Journal:  Eukaryot Cell       Date:  2006-01

4.  Cloning and sxpression of mitochondrial heat shock protein 70 of Trypanosoma congolense and potential use as a diagnostic antigen.

Authors:  Hiroshi Bannai; Tatsuya Sakurai; Noboru Inoue; Chihiro Sugimoto; Ikuo Igarashi
Journal:  Clin Diagn Lab Immunol       Date:  2003-09

5.  In situ structure of trypanosomal ATP synthase dimer reveals a unique arrangement of catalytic subunits.

Authors:  Alexander W Mühleip; Caroline E Dewar; Achim Schnaufer; Werner Kühlbrandt; Karen M Davies
Journal:  Proc Natl Acad Sci U S A       Date:  2017-01-17       Impact factor: 11.205

6.  Enigmatic presence of mitochondrial complex I in Trypanosoma brucei bloodstream forms.

Authors:  Sachin Surve; Meredith Heestand; Brian Panicucci; Achim Schnaufer; Marilyn Parsons
Journal:  Eukaryot Cell       Date:  2011-12-09

7.  Transcriptome-wide analysis of trypanosome mRNA decay reveals complex degradation kinetics and suggests a role for co-transcriptional degradation in determining mRNA levels.

Authors:  Abeer Fadda; Mark Ryten; Dorothea Droll; Federico Rojas; Valentin Färber; Jurgen R Haanstra; Clemetine Merce; Barbara M Bakker; Keith Matthews; Christine Clayton
Journal:  Mol Microbiol       Date:  2014-09-15       Impact factor: 3.501

8.  Three distinct isoforms of ATP synthase subunit c are expressed in T. brucei and assembled into the mitochondrial ATP synthase complex.

Authors:  Paul E Gulde; Linda Christen; Silvia V Brown; Noreen Williams
Journal:  PLoS One       Date:  2013-01-10       Impact factor: 3.240

9.  NADH dehydrogenase of Trypanosoma brucei is important for efficient acetate production in bloodstream forms.

Authors:  Sachin V Surve; Bryan C Jensen; Meredith Heestand; Muriel Mazet; Terry K Smith; Frédéric Bringaud; Marilyn Parsons; Achim Schnaufer
Journal:  Mol Biochem Parasitol       Date:  2016-10-04       Impact factor: 1.759

  9 in total

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