Literature DB >> 10431219

The endosymbiotic origin of the protein import machinery of chloroplastic envelope membranes.

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Abstract

Chloroplasts have evolved a complex proteinaceous machinery to import nuclear-encoded proteins. The origin of this machinery, following the endosymbiotic events leading to chloroplasts, is an intriguing, unresolved problem. Given that cyanobacteria are the probable ancestors of chloroplasts, the genome sequence of Synechocystis sp. PCC 6803 offers a valuable resource to identify putative homologs for components of this protein import machinery and to gain insights into its possibly endosymbiotic origin. Detailed computational sequence analysis reveals that Synechocystis sp. PCC 6803 has homologs of three of the known membrane proteins of the chloroplastic translocon, namely Toc75, Tic20 and Tic22, as well as a homolog of the putative component Tic55. Thus, the chloroplastic protein import machinery is mainly derived from the endosymbiotic cyanobacterium, but, interestingly, not from any of the four main protein secretion systems of prokaryotes. The relatively high sequence variability between chloroplastic and Synechocystis proteins suggests that the ancestral proteins had different physiological roles and were modified significantly to fulfill the new demand of importing proteins into the evolving chloroplast. The fact that some chloroplastic protein import components are not related to any Synechocystis proteins (Toc159, Tic110 and Toc34) indicates that the chloroplastic protein import apparatus is of a dual evolutionary origin.

Entities:  

Year:  1999        PMID: 10431219     DOI: 10.1016/s1360-1385(99)01449-1

Source DB:  PubMed          Journal:  Trends Plant Sci        ISSN: 1360-1385            Impact factor:   18.313


  25 in total

Review 1.  Arabidopsis genes encoding components of the chloroplastic protein import apparatus.

Authors:  D Jackson-Constan; K Keegstra
Journal:  Plant Physiol       Date:  2001-04       Impact factor: 8.340

2.  Identification of iron-responsive, differential gene expression in the cyanobacterium Synechocystis sp. strain PCC 6803 with a customized amplification library.

Authors:  A K Singh; L A Sherman
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

3.  Thylakoid targeting of Tat passenger proteins shows no delta pH dependence in vivo.

Authors:  Giovanni Finazzi; Claudia Chasen; Francis-André Wollman; Catherine de Vitry
Journal:  EMBO J       Date:  2003-02-17       Impact factor: 11.598

4.  Evidence that plant-like genes in Chlamydia species reflect an ancestral relationship between Chlamydiaceae, cyanobacteria, and the chloroplast.

Authors:  Fiona S L Brinkman; Jeffrey L Blanchard; Artem Cherkasov; Yossef Av-Gay; Robert C Brunham; Rachel C Fernandez; B Brett Finlay; Sarah P Otto; B F Francis Ouellette; Patrick J Keeling; Ann M Rose; Robert E W Hancock; Steven J M Jones; Hans Greberg
Journal:  Genome Res       Date:  2002-08       Impact factor: 9.043

Review 5.  Protein targeting into plastids: a key to understanding the symbiogenetic acquisitions of plastids.

Authors:  Ken-ichiro Ishida
Journal:  J Plant Res       Date:  2005-07-26       Impact factor: 2.629

Review 6.  Mitochondrial and plastid evolution in eukaryotes: an outsiders' perspective.

Authors:  Jeferson Gross; Debashish Bhattacharya
Journal:  Nat Rev Genet       Date:  2009-07       Impact factor: 53.242

7.  Role of temperature stress on chloroplast biogenesis and protein import in pea.

Authors:  Siddhartha Dutta; Sasmita Mohanty; Baishnab C Tripathy
Journal:  Plant Physiol       Date:  2009-04-29       Impact factor: 8.340

8.  Chloroplast Outer Membrane β-Barrel Proteins Use Components of the General Import Apparatus.

Authors:  Philip M Day; Kentaro Inoue; Steven M Theg
Journal:  Plant Cell       Date:  2019-06-19       Impact factor: 11.277

Review 9.  Evolution of protein transport to the chloroplast envelope membranes.

Authors:  Philip M Day; Steven M Theg
Journal:  Photosynth Res       Date:  2018-10-05       Impact factor: 3.573

10.  The prodomain of the Bordetella two-partner secretion pathway protein FhaB remains intracellular yet affects the conformation of the mature C-terminal domain.

Authors:  Christopher R Noël; Joseph Mazar; Jeffrey A Melvin; Jessica A Sexton; Peggy A Cotter
Journal:  Mol Microbiol       Date:  2012-10-05       Impact factor: 3.501

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