Control of Cajal body number is mediated by the coilin C-terminus
- 15 January 2003
- journal article
- Published by The Company of Biologists in Journal of Cell Science
- Vol. 116 (2) , 303-312
- https://doi.org/10.1242/jcs.00211
Abstract
Cajal bodies (CBs) are nuclear suborganelles implicated in the post-transcriptional maturation of small nuclear and small nucleolar RNAs. The number of CBs displayed by various cell lines and tissues varies, and factors that control CB numbers within a given cell have yet to be described. In this report, we show that specific regions within the C-terminus of coilin, the CB marker protein, are responsible for regulating the number of nuclear foci. Despite the fact that the coilin N-terminal domain is responsible for its self-oligomerization activity, truncation or mutation of predicted sites of phosphorylation in the conserved C-terminal region leads to a striking alteration in the number of nuclear bodies. Similarly, coilin constructs from various species display differential propensities to form nuclear foci when expressed in heterologous backgrounds. We mapped the domain responsible for this variability to the coilin C-terminus utilizing chimeric proteins. Furthermore, the activities responsible for regulating coilin self-association must reside in the nucleus, as constructs lacking critical nuclear localization sequences fail to form foci in the cytoplasm. Factors controlling the putative signal transduction cascade that phosphorylates coilin are also discussed. The results point to a model whereby phosphorylation of the coilin C-terminus regulates the availability of the N-terminal self-interaction domain.Keywords
This publication has 41 references indexed in Scilit:
- Cajal body-specific small nuclear RNAs: a novel class of 2'-O-methylation and pseudouridylation guide RNAsThe EMBO Journal, 2002
- Functional architecture in the cell nucleusBiochemical Journal, 2001
- A Role for the GSG Domain in Localizing Sam68 to Novel Nuclear Structures in Cancer Cell LinesMolecular Biology of the Cell, 1999
- Disruption of PML Subnuclear Domains by the Acidic IE1 Protein of Human Cytomegalovirus Is Mediated through Interaction with PML and May Modulate a RING Finger-Dependent Cryptic Transactivator Function of PMLMolecular and Cellular Biology, 1998
- Self-Association of the Single-KH-Domain Family Members Sam68, GRP33, GLD-1, and Qk1: Role of the KH DomainMolecular and Cellular Biology, 1997
- The SMN–SIP1 Complex Has an Essential Role in Spliceosomal snRNP BiogenesisCell, 1997
- Mutational analysis of p80 coilin indicates a functional interaction between coiled bodies and the nucleolus.The Journal of cell biology, 1995
- Structure, expression and chromosomal localization of human p80-coilin geneNucleic Acids Research, 1994
- Immunocytochemical analysis of the coiled body in the cell cycle and during cell proliferation.Proceedings of the National Academy of Sciences, 1993
- Assembly of snRNP-containing coiled bodies is regulated in interphase and mitosis--evidence that the coiled body is a kinetic nuclear structure.The Journal of cell biology, 1993