Title

Signal recognition particle components in the nucleolus

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Date

1-5-2000

Document Type

Article

Subjects

Animals; Cell Line; Cell Nucleolus; Endoplasmic Reticulum; Fluorescent Antibody Technique; Green Fluorescent Proteins; Humans; In Situ Hybridization; Luminescent Proteins; Molecular Sequence Data; RNA, Nuclear; Rats; Recombinant Fusion Proteins; *Saccharomyces cerevisiae Proteins; Signal Recognition Particle; Transfection

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

The signal recognition particle (SRP) is a ribonucleoprotein composed of an Alu domain and an S domain. The S domain contains unique sequence SRP RNA and four SRP proteins: SRP19, SRP54, SRP68, and SRP72. SRP interacts with ribosomes to bring translating membrane and secreted proteins to the endoplasmic reticulum (ER) for proper processing. Additionally, SRP RNA is a member of a family of small nonribosomal RNAs found recently in the nucleolus, suggesting that the nucleolus is more plurifunctional than previously realized. It was therefore of interest to determine whether other SRP components localize to this intranuclear site. In transfected rat fibroblasts, green fluorescent protein fusions of SRP19, SRP68, and SRP72 localized to the nucleolus, as well as to the cytoplasm, as expected. SRP68 also accumulated in the ER, consistent with its affinity for the ER-bound SRP receptor. SRP54 was detected in the cytoplasm as a green fluorescent protein fusion and in immunofluorescence studies, but was not detected in the nucleolus. In situ hybridization experiments also revealed endogenous SRP RNA in the nucleolus. These results demonstrate that SRP RNA and three SRP proteins visit the nucleolus, suggesting that partial SRP assembly, or another unidentified activity of the SRP components, occurs at the nucleolus. SRP54 apparently interacts with nascent SRP beyond the nucleolus, consistent with in vitro reconstitution experiments showing that SRP19 must bind to SRP RNA before SRP54 binds. Our findings support the notion that the nucleolus is the site of assembly and/or interaction between the family of ribonucleoproteins involved in protein synthesis, in addition to ribosomes themselves.

Rights and Permissions

Citation: Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):55-60.

Related Resources

Link to Article in PubMed

Journal Title

Proceedings of the National Academy of Sciences of the United States of America

PubMed ID

10618370