TY - JOUR
T1 - Conservation of expression and alternative splicing in the prosaposin gene
AU - Cohen, Tsadok
AU - Ravid, Liat
AU - Altman, Netta
AU - Madar-Shapiro, Liora
AU - Fein, Amos
AU - Weil, Miguel
AU - Horowitz, Mia
N1 - Funding Information:
We would like to thank Ms. Hassida Orenstein for preparing the slides for immunohistochemical analysis and to Mr. Tslil Ofir for electrophoresis of the sequencing gels and their quantitative analysis. This project was partially funded by grants from The Binational, Israel–USA, Science Foundation (BSF), The Israel Science Foundation (ISF) and Genzyme, USA (to MH).
PY - 2004/10/22
Y1 - 2004/10/22
N2 - Prosaposin is the precursor of four lysosomal activator molecules known as saposins A, B, C and D. It is also secreted and was proposed to be a neurotrophic factor. The neurotrophic function was attributed to the amino terminus of saposin C. In man, mouse and rat prosaposin is transcribed to two major isoforms differing in the inclusion of 9 bps of exon 8 within the saposin B domain. In the present study, we show that there is evolutionary conservation of the prosaposin structure and alternative splicing in chick and zebrafish as well. Moreover, there is conservation in prosaposin expression as tested immunohistochemically in the mouse and chick developing brain. We developed a sensitive assay to quantitate the prosaposin alternatively spliced forms. Our results indicate that, in mouse brain, skeletal and cardiac muscle the exon 8-containing RNA is most abundant, while it is almost absent from visceral and smooth muscle-containing organs. We observed temporal and differential expression of the alternatively spliced prosaposin mRNAs in mouse and chick brain as well as during development. The elevation in the abundance of exon 8-containing prosaposin RNA during mouse and chick brain development may suggest a role for the exon 8-containing prosaposin form in this process.
AB - Prosaposin is the precursor of four lysosomal activator molecules known as saposins A, B, C and D. It is also secreted and was proposed to be a neurotrophic factor. The neurotrophic function was attributed to the amino terminus of saposin C. In man, mouse and rat prosaposin is transcribed to two major isoforms differing in the inclusion of 9 bps of exon 8 within the saposin B domain. In the present study, we show that there is evolutionary conservation of the prosaposin structure and alternative splicing in chick and zebrafish as well. Moreover, there is conservation in prosaposin expression as tested immunohistochemically in the mouse and chick developing brain. We developed a sensitive assay to quantitate the prosaposin alternatively spliced forms. Our results indicate that, in mouse brain, skeletal and cardiac muscle the exon 8-containing RNA is most abundant, while it is almost absent from visceral and smooth muscle-containing organs. We observed temporal and differential expression of the alternatively spliced prosaposin mRNAs in mouse and chick brain as well as during development. The elevation in the abundance of exon 8-containing prosaposin RNA during mouse and chick brain development may suggest a role for the exon 8-containing prosaposin form in this process.
KW - Alternative splicing
KW - Prosaposin
KW - Saposins
UR - http://www.scopus.com/inward/record.url?scp=4644296741&partnerID=8YFLogxK
U2 - 10.1016/j.molbrainres.2004.06.027
DO - 10.1016/j.molbrainres.2004.06.027
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AN - SCOPUS:4644296741
SN - 0169-328X
VL - 129
SP - 8
EP - 19
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1-2
ER -