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Detection of mitochondrial transfer RNA (mt-tRNA) gene mutations in patients with idiopathic pulmonary fibrosis and sarcoidosis

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Autor
Daniil Z., Kotsiou O.S., Grammatikopoulos A., Peletidou S., Gkika H., Malli F., Antoniou K., Vasarmidi E., Mamuris Z., Gourgoulianis K., Zifa E.
Fecha
2018
Language
en
DOI
10.1016/j.mito.2018.10.004
Materia
mitochondrial transfer RNA
transfer RNA
unclassified drug
mitochondrial DNA
transfer RNA
5' flanking region
aged
Article
controlled study
female
fibrosing alveolitis
gene expression
gene identification
gene mutation
genetic association
human
lung sarcoidosis
major clinical study
male
priority journal
sequence analysis
adult
case control study
DNA sequence
fibrosing alveolitis
genetics
middle aged
mitochondrial gene
mutation
pathology
sarcoidosis
Adult
Aged
Case-Control Studies
DNA, Mitochondrial
Female
Genes, Mitochondrial
Humans
Idiopathic Pulmonary Fibrosis
Male
Middle Aged
Mutation
RNA, Transfer
Sarcoidosis
Sequence Analysis, DNA
Elsevier B.V.
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Resumen
Mitochondrial reactive oxygen species production may lead to tissue injury associated with two respiratory disorders of unknown origin which are shared by common tissue fibrosis, IPF and sarcoidosis. Sequence analysis of 22 mt-tRNA genes and parts of their flanking genes revealed 32 and 45 mutations in 38/40 IPF and 69/85 sarcoidosis patients respectively. 4 novel mutations were identified. 15/32 and 25/45 mutations were exclusively expressed while 12/32 and 17/45 mutations predominantly occurred in IPF and sarcoidosis group respectively, compared to healthy controls. Novel mutation combinations were solely expressed in disease. Hence, a mitochondrial-mediated pathogenic pathway seems to underlie both entities. © 2018 Elsevier B.V. and Mitochondria Research Society
URI
http://hdl.handle.net/11615/73062
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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