The common truncation variant in pancreatic lipase related protein 2 (PNLIPRP2) is expressed poorly and does not alter risk for chronic pancreatitis

A nonsense variant (p.W358X) of human pancreatic lipase related protein 2 (PNLIPRP2) is present in different ethnic populations with a high allele frequency. In cell culture experiments, the truncated protein mainly accumulates inside the cells and causes endoplasmic reticulum stress. Here, we teste...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Németh Balázs Csaba
Pesei Gabriella Zsófia
Hegyi Eszter
Szücs Ákos
Szentesi Andrea Ildikó
Hegyi Péter
Sahin-Tóth Miklós
Dokumentumtípus: Cikk
Megjelent: 2018
Sorozat:PLOS ONE 13 No. 11
doi:10.1371/journal.pone.0206869

mtmt:30316277
Online Access:http://publicatio.bibl.u-szeged.hu/17949
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520 3 |a A nonsense variant (p.W358X) of human pancreatic lipase related protein 2 (PNLIPRP2) is present in different ethnic populations with a high allele frequency. In cell culture experiments, the truncated protein mainly accumulates inside the cells and causes endoplasmic reticulum stress. Here, we tested the hypothesis that variant p.W358X might increase risk for chronic pancreatitis through acinar cell stress. We sequenced exon 11 of PNLIPRP2 in a cohort of 256 subjects with chronic pancreatitis (152 alcoholic and 104 non-alcoholic) and 200 controls of Hungarian origin. We observed no significant difference in the distribution of the truncation variant between patients and controls. We analyzed mRNA expression in human pancreatic cDNA samples and found the variant allele markedly reduced. We conclude that the p.W358X truncation variant of PNLIPRP2 is expressed poorly and has no significant effect on the risk of chronic pancreatitis. 
700 0 1 |a Pesei Gabriella Zsófia  |e aut 
700 0 1 |a Hegyi Eszter  |e aut 
700 0 1 |a Szücs Ákos  |e aut 
700 0 1 |a Szentesi Andrea Ildikó  |e aut 
700 0 1 |a Hegyi Péter  |e aut 
700 0 2 |a Sahin-Tóth Miklós  |e aut 
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