Two adjacent nuclear genes are required for functional complementation of a chloroplast <i>trans</i>‐splicing mutant from <i>Chlamydomonas reinhardtii</i>

Balczun, Carsten; Bunse, Astrid; Hahn, Daniela; Bennoun, Pierre; Nickelsen, Jörg; Kück, Ulrich

doi:10.1111/j.1365-313x.2005.02478.x

Cited by 47 publications

(56 citation statements)

References 50 publications

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“…Recent analysis of the nuclear pre-mRNA processing machinery revealed that proteins involved in RNA 3Ј-end processing are integral components of supraspliceosomes (44). This is reminiscent of the function of psaA splicing factors Rat2 and Raa1, which are both involved in 3Ј-end processing of the tscA RNA (15,22).…”

Section: Discussionmentioning

confidence: 99%

“…The RAT2 gene was previously identified in the C. reinhardtii class C trans-splicing mutant TR72:75, which shows a defect in trans-splicing of the chloroplast psaA mRNA and is crucial for 3Ј-end processing of the chloroplast tscA RNA (22). By using Raa4 as a bait, Rat2 was found among subcomplex I proteins (24).…”

Section: Core Components Of Trans-splicing Subcomplexes I and Ii-mentioning

confidence: 99%

“…C. reinhardtii total RNA isolation and RNA blot experiments were done as described previously (14,19,22). Transcripts were detected using radioactively labeled probes.…”

Section: Methodsmentioning

confidence: 99%

“…For C. reinhardtii, seven splicing factors, specific for group II introns, have been described at the molecular level (17)(18)(19)(20)(21)(22)(23). Whereas splicing factor Raa1 (RNA maturation of psaA RNA) is involved in splicing of both reactions, Raa3, Raa4, Raa8, and Rat2 (RNA maturation of psaA tscA RNA) are psaA-i1-specific.…”

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confidence: 99%

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

Reifschneider¹,

Marx²,

Jacobs³

et al. 2016

Journal of Biological Chemistry

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In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous group II introns, psaA-i1 and psaAi2, 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 chromatographymass 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.The spliceosome is a dynamic RNP machinery that participates in the excision of mRNA introns in eukaryotes. This machinery consists of five small nuclear RNAs (snRNAs; U1, U2, U4, U5, and U6) and a large number of spliceosomal proteins (1, 2). It is generally accepted that spliceosomal snRNAs were derived from ancient group II introns, which were introduced into the eukaryotic cell after endosymbiosis (3, 4). Group II introns occur frequently in bacteria and organelles of fungi, algae, and higher plants but are rare in archaea and absent from nuclear genomes. Comparable with spliceosomal introns, the splicing reaction includes two transesterification reactions, yielding spliced exons and an excised intron lariat RNA.Despite the lack of significant sequence similarities, group II introns share a common secondary structure with six helical domains (D1-D6) surrounding a central wheel. During intron excision, these domains take over specific functions, and remarkably, they show plenty of functional and structural similarities to spliceosomal snRNAs (5-7). These similarities led to the assumption that during evolution of the nuclear splicing apparatus, group II introns fragmented and degenerated to spliceosomal snRNAs (3,8,9).In contrast to bacterial group II introns, most organelle group II introns display variant forms of degeneration and fragmentation (9). For example, many of the plant group II introns have mispaired domain structures (10, 11). Moreover, group II introns are able to split into autonomous fragments due to rearrangements of organelle genomes (12, 13). Consequently, they are transcribed independently, and association of precursor RNAs by base pairing generates a catalytically active group II intron structure that is finally processed by trans-splicing. Such degenerated and fragmented group II introns along with the interplay of discrete RNAs during the splicing reaction serve to demonstrate how snRNAs...

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Section: Discussionmentioning

confidence: 99%

Section: Core Components Of Trans-splicing Subcomplexes I and Ii-mentioning

confidence: 99%

“…C. reinhardtii total RNA isolation and RNA blot experiments were done as described previously (14,19,22). Transcripts were detected using radioactively labeled probes.…”

Section: Methodsmentioning

confidence: 99%

mentioning

confidence: 99%

See 2 more Smart Citations

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

Reifschneider¹,

Marx²,

Jacobs³

et al. 2016

Journal of Biological Chemistry

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“…A remarkable result of our investigation was the detection of the functionally characterized splicing factors Raa1, Raa3, and Rat2, which all are involved in splicing of the first group II intron of the psaA precursor RNA (9,10,51) (Table I). Raa1 is also involved in the splicing of second group II intron of psaA pre-mRNA (52).…”

Section: Discussionmentioning

confidence: 99%

Identification of a Chloroplast Ribonucleoprotein Complex Containing Trans-splicing Factors, Intron RNA, and Novel Components

Jacobs

Marx

Kock

et al. 2013

Molecular & Cellular Proteomics

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Maturation of chloroplast psaA pre-mRNA from the green alga Chlamydomonas reinhardtii requires the trans-splicing of two split group II introns. Several nuclear-encoded trans-splicing factors are required for the correct processing of psaA mRNA. Among these is the recently identified Raa4 protein, which is involved in splicing of the tripartite intron 1 of the psaA precursor mRNA. Part of this tripartite group II intron is the chloroplast encoded tscA RNA, which is specifically bound by Raa4. Using Raa4 as bait in a combined tandem affinity purification and mass spectrometry approach, we identified core components of a multisubunit ribonucleoprotein complex, including three previously identified trans-splicing factors (Raa1, Raa3, and Rat2). We further detected tscA RNA in the purified protein complex, which seems to be specific for splicing of the tripartite group II intron. Intron-containing genes from prokaryotic or organellar genomes carry either group I or group II introns, each of which has distinct features. The splicing mechanism of group II introns and the secondary structures of their presumed active sites were used as early arguments for the hypothesis that this class of introns represents the ancestors of eukaryotic spliceosomal introns (1, 2). It was further assumed that group II introns invaded the eukaryotic nucleus and subsequently proliferated at various genomic sites, leading to the degeneration of the catalytic intron structure into small nuclear RNAs (snRNAs).1 This assumption was supported by the observation of naturally occurring variants of group II introns that are split into two or more pieces (3), reminiscent of eukaryotic spliceosomal RNA (1). Group II intron RNAs are characterized by six conserved domains, and tertiary interactions among these domains generate the compact native and catalytic complex. Some of these group II intron domains have been shown to act in trans on the splicing of other introns that lack the corresponding domain (4). In vivo, various RNA-binding proteins promote the formation of catalytically active intron RNA. In contrast to the nuclear spliceosome, which acts generally on a broad range of nuclear-encoded pre-mRNAs, proteins involved in organellar intron splicing seem to more efficiently stabilize the active three-dimensional RNA structure in vivo. Several splicing factors in higher plants, such as the chloroplast RNA-splicing and ribosome maturation (CRM) domain protein CRS1, as well as the pentatricopeptide repeat proteins OTP51 and PPR4, have been reported to be involved in the splicing of single transcripts (5, 6). Nonetheless, there are splicing factors that carry out functions on a broad range of transcripts, including CRS2 and its associated proteins CAF1 and CAF2, and WTF1, a splicing factor containing a plant organelle RNA-recognition domain (5, 6). Sedimentation and co-fractionation experiments in, for example, maize have demonstrated that these proteins are part of large multiprotein and ribonucleoprotein complexes with their cognate RNAs (5, 7). I...

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Trans‐splicing of organelle introns – a detour to continuous RNAs

Glanz

Kück

2009

BioEssays

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In eukaryotes, RNA trans-splicing is an important RNA-processing form for the end-to-end ligation of primary transcripts that are derived from separately transcribed exons. So far, three different categories of RNA trans-splicing have been found in organisms as diverse as algae to man. Here, we review one of these categories: the trans-splicing of discontinuous group II introns, which occurs in chloroplasts and mitochondria of lower eukaryotes and plants. Trans-spliced exons can be predicted from DNA sequences derived from a large number of sequenced organelle genomes. Further molecular genetic analysis of mutants has unravelled proteins, some of which being part of high-molecular-weight complexes that promote the splicing process. Based on data derived from the alga Chlamydomonas reinhardtii, a model is provided which defines the composition of an organelle spliceosome. This will have a general relevance for understanding the function of RNA-processing machineries in eukaryotic organelles.

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Two adjacent nuclear genes are required for functional complementation of a chloroplast trans‐splicing mutant from Chlamydomonas reinhardtii

Cited by 47 publications

References 50 publications

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

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

Identification of a Chloroplast Ribonucleoprotein Complex Containing Trans-splicing Factors, Intron RNA, and Novel Components

Trans‐splicing of organelle introns – a detour to continuous RNAs

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