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Enhanced SRSF5 Protein Expression Reinforces Lamin A mRNA Production in HeLa Cells and Fibroblasts of Progeria Patients
Author(s) -
Vautrot Valentin,
Aigueperse Christelle,
OilloBlanloeil Florence,
Hupont Sébastien,
Stevenin James,
Branlant Christiane,
BehmAnsmant Isabelle
Publication year - 2016
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.22945
Subject(s) - lmna , progeria , biology , lamin , mutation , rna splicing , intron , premature aging , microbiology and biotechnology , genetics , cancer research , rna , gene
The Hutchinson Gilford Progeria Syndrome (HGPS) is a rare genetic disease leading to accelerated aging. Three mutations of the LMNA gene leading to HGPS were identified. The more frequent ones, c.1824C>T and c.1822G>A, enhance the use of the intron 11 progerin 5′splice site (5′SS) instead of the LMNA 5′SS, leading to the production of the truncated dominant negative progerin. The less frequent c.1868C>G mutation creates a novel 5′SS (LAΔ35 5′SS), inducing the production of another truncated LMNA protein (LAΔ35). Our data show that the progerin 5′SS is used at low yield in the absence of HGPS mutation, whereas utilization of the LAΔ35 5′SS is dependent upon the presence of the c.1868C>G mutation. In the perspective to correct HGPS splicing defects, we investigated whether SR proteins can modify the relative yields of utilization of intron 11 5′SSs. By in cellulo and in vitro assays, we identified SRSF5 as a direct key regulator increasing the utilization of the LMNA 5′SS in the presence of the HGPS mutations. Enhanced SRSF5 expression in dermal fibroblasts of HGPS patients as well as PDGF‐BB stimulation of these cells decreased the utilization of the progerin 5′SS, and improves nuclear morphology, opening new therapeutic perspectives for premature aging.