A perinucleolar compartment contains several RNA polymerase III transcripts as well as the polypyrimidine tract-binding protein, hnRNP I [published erratum appears in J Cell Biol 1995 Jul;130(2):497-500]
Open Access
- 1 June 1995
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 129 (5), 1181-1193
- https://doi.org/10.1083/jcb.129.5.1181
Abstract
We have investigated the subcellular organization of the four human Y RNAs. These RNAs, which are transcribed by RNA polymerase III, are usually found complexed with the Ro autoantigen, a 60-kD protein. We designed 2'-OMe oligoribonucleotides that were complementary to accessible single-stranded regions of Y RNAs within Ro RNPs and used them in fluorescence in situ hybridization. Although all four Y RNAs were primarily cytoplasmic, oligonucleotides directed against three of the RNAs hybridized to discrete structures near the nucleolar rim. We have termed these structures "perinucleolar compartments" (PNCs). Double labeling experiments with appropriate antisera revealed that PNCs are distinct from coiled bodies and fibrillar centers. Co-hybridization with a genomic DNA clone spanning the human Y1 and Y3 genes showed that PNCs are not stably associated with the transcription site for these Y RNAs. Although 5S rDNA was often located near the nucleolar periphery, PNCs are not associated with 5S gene loci. Two additional pol III transcripts, the RNA components of RNase P and RNase MRP, did colocalize within PNCs. Most interestingly, the polypyrimidine tract-binding protein hnRNP I/PTB was also concentrated in this compartment. Possible roles for this novel nuclear subdomain in macromolecular assembly and/or nucleocytoplasmic shuttling of these five pol III transcripts, along with hnRNP I/PTB, are discussed.Keywords
This publication has 51 references indexed in Scilit:
- A possible role for the 60-kD Ro autoantigen in a discard pathway for defective 5S rRNA precursors.Genes & Development, 1994
- Nucleologenesis: U3 snRNA-containing prenucleolar bodies move to sites of active pre-rRNA transcription after mitosis.Molecular Biology of the Cell, 1994
- The RNA of RNase MRP is required for normal processing of ribosomal RNA.Proceedings of the National Academy of Sciences, 1994
- Nucleoplasmic organization of small nuclear ribonucleoproteins in cultured human cells.The Journal of cell biology, 1993
- hnRNP 1, the polyprimidine tract-binding protein: distinct nuclear localization and association with hnRNAsNucleic Acids Research, 1992
- Characterization of cDNAs encoding the polypyrimidine tract-binding protein.Genes & Development, 1991
- High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid ClonesScience, 1990
- The Ro ribonucleoprotein particle: Induction of autoantibodies and the detection of Ro RNAs among speciesClinical Immunology and Immunopathology, 1989
- A mammalian mitochondrial serine transfer RNA lacking the “dihydrouridine” loop and stemNucleic Acids Research, 1980
- Site specific enzymatic cleavage of RNANucleic Acids Research, 1979