Up-regulation of human PNPase mRNA by beta-interferon has no effect on protein level in melanoma cell lines.
Author(s) -
Kamil Gewartowski,
Rafał Tomecki,
Lukasz Muchowski,
Aleksandra Dmochow Ska,
Artur Dzwonek,
Michał Małecki,
H Skurzak,
Jerzy Ostrowski,
Piotr P. Stȩpień
Publication year - 2006
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2006_3376
Subject(s) - polynucleotide phosphorylase , messenger rna , hela , melanoma , exoribonuclease , interferon , jurkat cells , mitochondrion , microbiology and biotechnology , purine nucleoside phosphorylase , cell culture , protein biosynthesis , cell , biology , chemistry , cancer research , enzyme , rna , immunology , gene , rnase p , biochemistry , t cell , genetics , immune system , purine
Human mitochondrial polynucleotide phosphorylase (hPNPase) is an exoribonuclease localized in mitochondria. The exact physiological function of this enzyme is unknown. Recent studies have revealed the existence of a relationship between induction of hPNPase mRNA and both cellular senescence and growth arrest of melanoma cells following beta-interferon treatment. The aim of this study was to verify whether the augmented hPNPase mRNA level results in increase of the protein level. In several cell lines established from five metastatic melanoma patients we did not find any such correlation. However, an elevated level of hPNPase protein was observed in interferon-induced HeLa and Jurkat cells. This increase was correlated with a slight shortening of poly(A) tails of mitochondrial ND3 transcript.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom