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A Ribonucleoprotein Supercomplex Involved in trans-Splicing of Organelle Group II Introns.


ABSTRACT: In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous group II introns, psaA-i1 and psaA-i2, splice in trans, and thus their excision process resembles the nuclear spliceosomal splicing pathway. Here, we address the question whether fragmentation of trans-acting RNAs is accompanied by the formation of a chloroplast spliceosome-like machinery. Using a combination of liquid chromatography-mass spectrometry (LC-MS), size exclusion chromatography, and quantitative RT-PCR, we provide the first characterization of a high molecular weight ribonucleoprotein apparatus participating in psaA mRNA splicing. This supercomplex contains two subcomplexes (I and II) that are responsible for trans-splicing of either psaA-i1 or psaA-i2. We further demonstrate that both subcomplexes are associated with intron RNA, which is a prerequisite for the correct assembly of subcomplex I. This study contributes further to our view of how the eukaryotic nuclear spliceosome evolved after bacterial endosymbiosis through fragmentation of self-splicing group II introns into a dynamic, protein-rich RNP machinery.

SUBMITTER: Reifschneider O 

PROVIDER: S-EPMC5087748 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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A Ribonucleoprotein Supercomplex Involved in trans-Splicing of Organelle Group II Introns.

Reifschneider Olga O   Marx Christina C   Jacobs Jessica J   Kollipara Laxmikanth L   Sickmann Albert A   Wolters Dirk D   Kück Ulrich U  

The Journal of biological chemistry 20160919 44


In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous group II introns, psaA-i1 and psaA-i2, splice in trans, and thus their excision process resembles the nuclear spliceosomal splicing pathway. Here, we address the question whether fragmentation of trans-acting RNAs is accompanied by the formation of a chloroplast spliceosome-like machinery. Using a combination of liquid chromatography-mass spectrometry (LC-MS), size exclusion chromatography, and quantitative RT-PCR,  ...[more]

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