Association of FMRP with ribosomal precursor particles in the nucleolus.

Abstract:

:The fragile X syndrome, one of the most common forms of inherited mental retardation, is caused by an expansion of a polymorphic CGG repeat upstream the coding region of the FMR1 gene. These expansions are associated with hypermethylation of the FMR1 gene, which results in the absence of the gene product, the FMR1 protein (FMRP). The physiological function of FMRP remains to be determined. We studied the ultrastructural localization of FMRP at the electron microscopical level using the immunogold technique. FMRP is associated with ribosomes attached to the endoplasmic reticulum and with ribosomes free in the cytoplasm. In addition, FMRP is found in the nucleus where the protein is associated with the granular component of the nucleolus. The cellular function of FMRP is hypothesized in relation to its subcellular distribution.

authors

Willemsen R,Bontekoe C,Tamanini F,Galjaard H,Hoogeveen A,Oostra B

doi

10.1006/bbrc.1996.1126

subject

Has Abstract

pub_date

1996-08-05 00:00:00

pages

27-33

issue

1

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(96)91126-2

journal_volume

225

pub_type

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