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Subcellular partitioning of MRP RNA assessed by ultrastructural and biochemical analysis
K Li1, C S Smagula, W J Parsons
1Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235.
Abstract:
A small RNA encoded within the nucleus is an essential subunit of a RNA processing endonuclease (RNase MRP) hypothesized to generate primers for mitochondrial DNA replication from the heavy strand origin of replication. Controversy has arisen, however, concerning the authenticity of an intramitochondrial pool of MRP RNA, and has called into question the existence of pathways for nucleo-mitochondrial transport of nucleic acids in animal cells. In an effort to resolve this controversy, we combined ultrastructural in situ hybridization and biochemical techniques to assess the subcellular partitioning of MRP RNA. Cryosections of mouse cardiomyocytes were hybridized with biotin-labeled RNA probes complementary to different regions of MRP RNA and varying in length from 115 to 230 nucleotides, followed by immunogold labeling. In addition, we transfected mouse C2C12 myogenic cells with constructs bearing mutated forms of the mouse MRP RNA gene and compared the relative abundance of the resulting transcripts to that of control RNAs within whole cell and mitochondrial fractions. In the former analysis we observed preferential localization of MRP RNA to nucleoli and mitochondria in comparison to the nucleoplasm and cytoplasm. In the latter series of studies we observed that wild-type MRP RNA partitions to the mitochondrial fraction by comparison to other RNA transcripts that are localized to the extramitochondrial cytoplasmic space (28S rRNA) or to the nucleoplasm (U1 snRNA). Deletions within 5' or 3' regions of the MRP RNA gene produced transcripts that remain competent for mitochondrial targeting. In contrast, deletion of the midportion of the coding region (nt 118 to 175) of the MRP RNA gene resulted in transcripts that fail to partition to the mitochondrial fraction. We conclude that an authentic intramitochondrial pool of MRP RNA is present in these actively respiring cells, and that specific structural determinants within the MRP RNA molecule permit it to be partitioned to mitochondria.
Insights
This study confirms an authentic intramitochondrial pool of MRP RNA in actively respiring cells. Specific structural elements within MRP RNA enable its transport and localization to mitochondria.
Area of Science:
- Cell Biology
- Molecular Biology
- Mitochondrial Biology
Background:
- Ribonucleic acid processing endonuclease (RNase MRP) is crucial for mitochondrial DNA replication.
- The existence of intramitochondrial MRP RNA and nucleo-mitochondrial transport pathways has been debated.
- Investigating MRP RNA's subcellular localization is key to understanding its function.
Purpose of the Study:
- To resolve controversy regarding the presence of MRP RNA within mitochondria.
- To investigate the mechanisms of nucleo-mitochondrial transport of MRP RNA.
- To identify structural determinants of MRP RNA responsible for mitochondrial targeting.
Main Methods:
- Ultrastructural in situ hybridization on mouse cardiomyocyte cryosections with biotin-labeled RNA probes.
- Immunogold labeling to detect MRP RNA localization.
- Transfection of mouse C2C12 cells with mutated MRP RNA gene constructs and analysis of RNA fractions.
Main Results:
- MRP RNA showed preferential localization to nucleoli and mitochondria.
- Wild-type MRP RNA partitioned to the mitochondrial fraction, unlike cytoplasmic (28S rRNA) or nucleoplasmic (U1 snRNA) RNAs.
- Mutations in the central coding region (nt 118-175) of MRP RNA abolished mitochondrial targeting, while 5' or 3' deletions did not.
Conclusions:
- An authentic intramitochondrial pool of MRP RNA exists in actively respiring cells.
- Specific structural determinants within the MRP RNA molecule are essential for its mitochondrial partitioning.
- These findings support the role of MRP RNA in mitochondrial DNA replication initiation.