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Differential, regional, and cellular expression of the stathmin family transcripts in the adult rat brain
Author(s) -
Ozon Sylvie,
El Mestikawy Salah,
Sobel André
Publication year - 1999
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/(sici)1097-4547(19990601)56:5<553::aid-jnr11>3.0.co;2-j
Subject(s) - stathmin , phosphoprotein , biology , in situ hybridization , microbiology and biotechnology , gene expression , gene , phosphorylation , genetics
Stathmin is a ubiquitous cytosolic phosphoprotein, preferentially expressed in the nervous system, and previously described as a relay integrating diverse intracellular signaling pathways. Stathmin is the generic element of a mammalian protein family including SCG10, SCLIP, and RB3 with its splice variants RB3′ and RB3″. In contrast with stathmin, SCG10, SCLIP, and RB3/RB3′/RB3″ are exclusively expressed in the nervous system, stathmin and SCG10 being mostly expressed during cell proliferation and differentiation, and SCLIP and RB3 rather in mature neural cells. To further understand their specific roles in the CNS, we compared the localization of the stathmin, SCG10, SCLIP, and RB3 transcripts in adult rat brain. Northern blot analysis as well as in situ hybridization experiments showed that all stathmin‐related mRNAs are expressed in a wide range of adult rat brain areas. At a regional level, SCG10 and SCLIP appear generally distributed similarly except in a few areas. The pattern of expression of the RB3 transcript is very different from that of the three other members of the stathmin family. Furthermore, unlike SCG10 and SCLIP, which were detected only in neurons, but like stathmin, RB3 was detected in neurons and also in glial cells of the white matter. Altogether, our results suggest distinct roles for each member of the stathmin‐related phosphoprotein family, in regard to their specific regional and cellular localization in the rat brain. J. Neurosci. Res. 56:553–564, 1999. © 1999 Wiley‐Liss, Inc.