Hypoxia-inducible myoglobin expression in nonmuscle tissues

Jane Fraser, Luciane Vieira De Mello, Deborah Ward, Huw H. Rees, Daryl R. Williams, Yongchang Fang, Andrew Brass, Andrew Y. Gracey, Andrew R. Cossins

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Myoglobin (Myg) is an oxygen-binding hemoprotein that is widely thought to be expressed exclusively in oxidative skeletal and cardiac myocytes, where it plays a key role in coping with chronic hypoxia. We now show in a hypoxia-tolerant fish model, that Myg is also expressed in a range of other tissues, including liver, gill, and brain. Moreover, expression of Myg transcript was substantially enhanced during chronic hypoxia, the fold-change induction being far greater in liver than muscle. By using 2D gel electrophoresis, we have confirmed that liver expresses a protein corresponding to the Myg-1 transcript and that it is significantly up-regulated during hypoxia. We have also discovered a second, unique Myg isoform, distinct from neuroglobin, which is expressed exclusively in the neural tissue but whose transcript expression was unaffected by environmental hypoxia. Both observations of nonmuscle expression and a brain-specific isoform are unprecedented, indicating that Myg may play a much wider role than previously understood and that Myg might function in the protection of tissues from deep hypoxia and ischemia as well as in reoxygenation and reperfusion injury. © 2006 by The National Academy of Sciences of the USA.
    Original languageEnglish
    Pages (from-to)2977-2981
    Number of pages4
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume103
    Issue number8
    DOIs
    Publication statusPublished - 21 Feb 2006

    Keywords

    • Globin expression
    • Hypoxia adaptation
    • Microarray
    • Proteomics

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