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Differential expression of Dp71 and Dp40 isoforms in proliferating and differentiated neural stem cells: Identification of Dp40 splicing variants.

Authors :
Paúl-González, Sandra
Aragón, Jorge
Rodríguez-Martínez, Griselda
Romo-Yáñez, José
Montanez, Cecilia
Source :
Biochemical & Biophysical Research Communications. Jun2021, Vol. 560, p152-158. 7p.
Publication Year :
2021

Abstract

Dp71 and Dp40 are the main products of the DMD gene in the central nervous system, and they are developmentally regulated from the early stages of embryonic development to adulthood. To further study the roles of Dp71 and Dp40 during cell proliferation and neural differentiation, we analyzed Dp71/Dp40 isoform expression at the mRNA level by RT-PCR assays to identify alternative splicing (AS) in the isoforms expressed in rat neural stem/progenitor cells (NSPCs) and in differentiated cells (neurons and glia). We found that proliferating NSPCs expressed Dp71d, Dp71d Δ71 , Dp71f, Dp71f Δ71 , Dp71d Δ74 and Dp40, as well as two Dp40 isoforms: Dp40 Δ63,64 and Dp40 Δ64-67. In differentiated cells we also found the expression of Dp71d, Dp71d Δ71 , Dp71f, Dp71f Δ71 and Dp40. However, the expression frequencies were different in both stages. In addition, in differentiated cells, we found Dp71f Δ71-74 , and interestingly, we did not find the expression of Dp71d Δ74 or the newly identified Dp40 isoforms. In this work we show that NSPC differentiation is accompanied by changes in Dp71/Dp40 isoform expression, suggesting different roles for these isoforms in NSPCs proliferation and neuronal differentiation, and we describe, for the first time, alternative splicing of Dp40. • Proliferating NSPCs differentially expressed Dp71 and Dp40 isoforms. • Dp71d isoforms are highly expressed in NSPCs. • Proliferating NSPCs expressed novel Dp40 isoforms Dp40 Δ63,64 and Dp40 Δ64-67. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
560
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
150465138
Full Text :
https://doi.org/10.1016/j.bbrc.2021.03.142