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Analysis of Expression Profiles of Genes Involved in F0F1-ATP Synthase Biogenesis During Perinatal Development in Rat Liver and Skeletal Muscle

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F16%3A10329192" target="_blank" >RIV/00216208:11110/16:10329192 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064165:_____/16:10329192

  • Result on the web

    <a href="http://www.biomed.cas.cz/physiolres/pdf/65/65_597.pdf" target="_blank" >http://www.biomed.cas.cz/physiolres/pdf/65/65_597.pdf</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Analysis of Expression Profiles of Genes Involved in F0F1-ATP Synthase Biogenesis During Perinatal Development in Rat Liver and Skeletal Muscle

  • Original language description

    During the process of intrauterine mammalian fetal development, the oxygen supply in growing fetus is low. A rapid switch from glycolysis based metabolism to oxidative phosphorylation (OXPHOS) must proceed during early postnatal adaptation to extra uterine conditions. Mitochondrial biogenesis and mammalian mitochondrial F0F1 ATP synthase assembly (complex V, EC 3.6.3.14, ATPase) are complex processes regulated by multiple transcription regulators and assembly factors. Using RNA expression analysis of rat liver and skeletal tissue (Rattus norvegicus, Berkenhout, 1769), we describe the expression profiles of 20 genes involved in mitochondrial maturation and ATP synthase biogenesis in detail between the 16th and 22nd day of gestation and the first 4 days of life. We observed that the most important expression shift occurred in the liver between the 20th and 22nd day of gestation, indicating that the fetus prepares for birth about two days before parturition. The detailed mechanism regulating the perinatal adaptation process is not yet known. Deeper insights in perinatal physiological development will help to assess mitochondrial dysfunction in the broader context of cell metabolism in preterm newborns or neonates with poor adaptation to extra uterine life.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GB14-36804G" target="_blank" >GB14-36804G: Centre of mitochondrial biology and pathology (MITOCENTRE)</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2016

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Physiological Research

  • ISSN

    0862-8408

  • e-ISSN

  • Volume of the periodical

    65

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    12

  • Pages from-to

    597-608

  • UT code for WoS article

    000386685600007

  • EID of the result in the Scopus database

    2-s2.0-84997501404