Nucleolar localization of the Werner Syndrome protein in human cells

Robert A Marciniak, David B. Lombard, F. Bradley Johnson, Leonard Guarente

Research output: Contribution to journalArticle

172 Citations (Scopus)

Abstract

Werner Syndrome (WS) is a human genetic disorder with many features of premature aging. The gene defective in WS (WRN) has been cloned and encodes a protein homologous to several helicases, including Escherichia coli RecQ, the human Bloom syndrome protein (BLM), and Saccharomyces cerevisiae Sgs1p. To better define the function of WRN protein we have determined its subcellular localization. Indirect immunofluorescence using polyclonal anti-human WRN shows a predominant nucleolar localization. Studies of WRN mutant cells lines confirmed the specificity of antibody recognition. No difference was seen in the subcellular localization of the WRN protein in a variety of normal and transformed human cell lines, including both carcinomas and sarcomas. The nucleolar localization of human WRN protein was supported by the finding that upon biochemical subcellular fractionation, WRN protein is present in an increased concentration in a subnuclear fraction enriched for nucleolar proteins. We have also determined the subcellular localization of the mouse WRN homologue (mWRN). In contrast to human WRN protein, mWRN protein is present diffusely throughout the nucleus. Understanding the function of WRN in these organisms of vastly differing lifespan may yield new insights into the mechanisms of lifespan determination.

Original languageEnglish (US)
Pages (from-to)6887-6892
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume95
Issue number12
DOIs
StatePublished - Jun 9 1998
Externally publishedYes

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Werner Syndrome
Proteins
Premature Aging
Transformed Cell Line
Inborn Genetic Diseases
Antibody Specificity
Medical Genetics
Indirect Fluorescent Antibody Technique
Nuclear Proteins
Sarcoma
Saccharomyces cerevisiae
Escherichia coli
Carcinoma
Cell Line
Genes

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

Nucleolar localization of the Werner Syndrome protein in human cells. / Marciniak, Robert A; Lombard, David B.; Johnson, F. Bradley; Guarente, Leonard.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, No. 12, 09.06.1998, p. 6887-6892.

Research output: Contribution to journalArticle

Marciniak, Robert A ; Lombard, David B. ; Johnson, F. Bradley ; Guarente, Leonard. / Nucleolar localization of the Werner Syndrome protein in human cells. In: Proceedings of the National Academy of Sciences of the United States of America. 1998 ; Vol. 95, No. 12. pp. 6887-6892.
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