Mitochondria-associated satellite I RNA binds to hnRNP K protein.

  • Karolina Klimek-Tomczak Department of Gastroenterology, Medical Center for Postgraduate Education and the Maria Skłodowska-Curie Memorial Cancer Center and Institute of Oncology, Warszawa, Poland.;
  • Michał Mikula
  • Artur Dzwonek
  • Agnieszka Paziewska
  • Lucjan S Wyrwicz
  • Ewa E Hennig
  • Jerzy Ostrowski

Abstract

hnRNP K protein, which localizes to the nucleus, cytoplasm and mitochondria, is involved in the various cellular processes that compose gene expression. We used a SAGE-based assay to profile RNAs associated with hnRNP K protein in rat mitochondria. RNA was isolated from mitoplasts obtained from highly purified and RNase-treated mitochondria. Total RNA and RNA associated with hnRNP K protein were then used as input material for generating two SAGE libraries. Mitochondrion-derived tags isolated from the total mitoplast RNA library represented 86.3%, while those isolated from the library constructed from RNA associated with hnRNP K protein represented only 28.2% of selected tags. Thus, an unexpected number of nuclear-encoded RNAs were purified from mitochondria. Many of these transcripts were co-purified with hnRNP K protein, and high levels of nuclear-encoded RNAs co-immunoprecipitating with K protein corresponded to elevated hnRNP K protein levels of the organelle. The most abundant RNAs that were co-purified with hnRNP K protein represented transcripts originating from satellite I DNA. While satellite I RNA levels were higher in the nucleus and cytoplasm than in mitochondria, the most abundant binding of satellite I transcripts to hnRNP K protein was found in mitochondria. The role of satellite I RNA in mitochondria remains to be elucidated.
Published
2006-02-23
Section
Articles