Jump to ContentJump to Main Navigation

Biological Chemistry

Editor-in-Chief: Brüne, Bernhard

Editorial Board Member: Buchner, Johannes / Ludwig, Stephan / Sies, Helmut / Turk, Boris / Wittinghofer, Alfred

12 Issues per year

Access brought to you by:

provisional account

VolumeIssuePage

Issues

Differential accumulation of plastid preprotein translocon components during spruce (Picea abies L. Karst.) needle development

Hrvoje Fulgosi1 / Hrvoje Lepeduš2 / Vera Cesar3 / Nikola Ljubešić4

1.

2.

3.

4.

Corresponding author

Citation Information: Biological Chemistry. Volume 386, Issue 8, Pages 777–783, ISSN (Online) 1437-4315, ISSN (Print) 1431-6730, DOI: 10.1515/BC.2005.091, September 2005

Publication History

Received:
March 29, 2005
Accepted:
June 6, 2005
Published Online:
2005-09-06

Abstract

We demonstrate that basic components of the plastid protein-import apparatus originally found in pea, Toc34, Toc159, and Tic110, are also conserved in evolutionarily younger gymnosperms. We show that multiple isoforms of the preprotein receptor Toc34 differentially accumulate in various stages of needle development, while the amounts of Toc159 drastically decrease during chloroplast morphogenesis. Spruce Toc34 and Toc159 receptors are able to recognise and interact with the angiosperm precursor of the Rubisco small subunit. Young proplastids found in closed buds contain a highly elevated number of protein translocation complexes equipped with only two types of outer envelope receptors, Toc159 and a 30-kDa Toc34-related protein. Photosystem II (PSII) can already be assembled in a fully functional complex at this very early stage of needle development, suggesting that no additional receptor isoforms are needed for translocation of all necessary PSII components. We conclude that the accumulation of evolutionarily conserved plastid preprotein translocation components is differentially regulated during spruce needle development.

Keywords: plastid biogenesis; proplastids; protein translocation; Tic; Toc

References

Comments (0)

Please log in or register to comment.