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Dual REST‐dependence of L1CAM: from gene expression to alternative splicing governed by Nova2 in neural cells
Author(s) -
Mikulak Joanna,
Negrini Sara,
Klajn Andrijana,
D’Alessandro Rosalba,
Mavilio Domenico,
Meldolesi Jacopo
Publication year - 2012
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2011.07626.x
Subject(s) - alternative splicing , neural cell adhesion molecule , gene isoform , rna splicing , biology , microbiology and biotechnology , exon , l1 , cell adhesion molecule , rest (music) , cell adhesion , repressor , transcription factor , gene , cell , genetics , rna , medicine
J. Neurochem (2012) 120 , 699–709. Abstract L1 cell adhesion molecule (L1CAM), an adhesion/signaling protein encoded by a gene target of the transcription repressor RE‐1‐Silencing Transcription factor (REST), is expressed in two alternatively spliced isoforms. The full‐length isoform, typical of low‐REST neural cells, plays key roles in survival/migration, outgrowth/fasciculation/regeneration of axons, synaptic plasticity; the isoform missing two mini‐exons, abundant in a few high‐REST non‐neural cells, maintains some effect on migration and proliferation. To investigate whether and how L1CAM alternative splicing depends on REST we used neural cell models expressing low or high levels of REST (PC12, SH‐SY5Y, differentiated NT2/D1 and primary neurons transduced or not with REST). The short isoform was found to rise when the low‐REST levels of neural cells were experimentally increased, while the full‐length isoform increased in high‐REST cells when the repressor tone was attenuated. These results were due to Nova2, a neural cell‐specific splicing factor shown here to be repressed by REST. REST control of L1CAM occurs therefore by two mechanisms, transcription and alternative splicing. The splicing mechanism, affecting not only L1CAM but all Nova2 targets (∼7% of brain‐specific splicing, including the mRNAs of other adhesion and synaptic proteins) is expected to be critical during development and important also for the structure and function of mature neural cells.