Human adipose and skeletal muscle tissue DNA, RNA, and protein content

JOURNAL OF APPLIED PHYSIOLOGY(2021)

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摘要
The purpose of this project was to provide a profile of DNA, RNA, and protein content in adipose tissue, which is relatively understudied in humans, to gain more insight into the amount of tissue that may be required for various analyses. Skeletal muscle tissue was also investigated to provide a direct comparison into potential differences between these two highly metabolically active tissues. Basal adipose and skeletal muscle tissue samples were obtained from 10 (7 M, 3 W) recreationally active participants [25 +/- 1 yr; 84 +/- 3 kg, maximal oxygen consumption ((V)over doto(2max)): 3.5 +/- 0.2 L/min, body fat: 29 +/- 2%]. DNA, RNA, and protein were extracted and subsequently analyzed for quantity and quality. DNA content of adipose and skeletal muscle tissue was 52 +/- 14 and 189 +/- 44 ng DNA.mg tissue(-1), respectively (P < 0.05). RNA content of adipose and skeletal muscle tissue was 46 +/- 14 and 537 +/- 72 ng RNA.mg tissue(-1), respectively (P < 0.05). Protein content of adipose and skeletal muscle tissue was 4 +/- 1 and 177 +/- 10 mu g protein.mg tissue(-1), respectively (P < 0.05). In summary, human adipose had 28% of the DNA, 9% of the RNA, and 2% of the protein found in skeletal muscle per mg of tissue. This information should be useful across a wide range of human clinical investigation designs and various laboratory analyses. NEW & NOTEWORTHY This investigation studied DNA, RNA, and protein contents of adipose and skeletal muscle tissues from young active individuals. A series of optimization steps were investigated to aid in determining the optimal approach to extract high-yield and high-quality biomolecules. These findings contribute to the knowledge gap in adipose tissue requirements for molecular biology assays, which is of increasing importance due to the growing interest in adipose tissue research involving human exercise physiology research.
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关键词
adipose, DNA, protein, RNA, skeletal muscle
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