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Vol41 No.4: 280-284

 

Expression of cytosolic 5' nucleotidase does not correlate with expression of oxidative metabolism marker: myoglobine in human skeletal muscles

 

Katarzyna Lechward* and Kinga Tkacz-Stachowska

 

(Department of Molecular Enzymology, Intercollegiate Faculty of Biotechnology, Medical University of Gdansk, Gdansk, Poland)

 

Abstract
����Our previous studies had shown that cytosolic 5' nucleotidase-I (cN-I) is expressed in several tissues in pigeons, including brain and several different skeletal muscles. We observed that cN-I mRNA levels varied among different pigeon muscles. Initial quantification of the differences revealed that ~5�C10 times more of cN-I transcript was present in red, oxidative muscles (breast muscle and gastrocnemius) than in white ones, composed of glycolytic fibers (biceps brachii). We had found this observation very intriguing and decided to
    compare human skeletal muscles distribution of cN-I with the type of oxygen metabolism. Our screen involved 60 samples of several human muscles and we
    assayed the correlation between the amount of transcripts of cN-I and myoglobine, which we took as a measure of oxidative-slow twitch fibers. Our question was whether in humans, cN-I presence in skeletal muscles was related to their fiber composition. If that was the case, then cN-I expression could serve as a tool to assess the percentage of oxidative fibers in any given
    human muscle sample, where myoglobine expression could not be readily measured. After quantification of expression of both genes, we concluded that there was no correlation between expression of cN-I and fiber type. Therefore, contrary to the pigeon muscles, cN-I did not reflect the ratio of oxidative fibers to the total mass of the muscle sample in humans. That difference
    indicated that there were certain mechanisms that differentially regulated the expression of cN-I in muscle tissues of mammals and lower vertebrates.

 

Received: 2008-11-18����Accepted: 2009-2-11

 

*Corresponding author . Tel: +48-58-3491470; Fax: +48-58-3491445; E-mail: [email protected]

 

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