Comparison of aquaporin-1 expression between yak (Bos grunniens) and indigenous cattle (Bos taurus) in the Qinghai–Tibetan Plateau
C. L. Zhong A B , J. P. Kang A B , G. S. Stewart D , J. W. Zhou A B , X. D. Huang B , J. D. Mi B C , J. Liu A B , C. Yang A B , Y. Zhang B and R. J. Long A B C EA State Key Laboratory of Grassland and Agro-Ecosystems, College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou 730000, China.
B International Centre for Tibetan Plateau Ecosystem Management, Lanzhou University, Lanzhou 730000, China.
C School of Life Sciences, Lanzhou University, Lanzhou 730000, China.
D School of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland.
E Corresponding author. Email: longrj@lzu.edu.cn
Animal Production Science 57(8) 1618-1623 https://doi.org/10.1071/AN15702
Submitted: 5 October 2015 Accepted: 14 January 2016 Published: 23 March 2016
Abstract
Aquaporins (AQPs) are a large family of integral membrane proteins that facilitate the transport of water through the biomembranes. AQP1, one of the 13 AQPs identified in mammals, is distributed in various tissues and organs, and plays an important role in body water homeostasis. The objectives of the present study were to identify the expression of aquaporin-1 (AQP1) in the kidney, rumen and parotid gland of yaks, and to quantify whether the protein abundance of AQP1 is species specific between yak (Bos grunniens) and indigenous cattle (Bos taurus). Three 3-year-old castrated males (156 ± 6.8 kg of bodyweight) of each of three genotypes, namely, yak, indigenous cattle and the crossbred between the two (Bos taurus♂ × Bos grunniens♀), were used; all animals were grazed in the same autumn pasture of the Qinghai–Tibetan Plateau, China. Western blot results detected (1) 28-kDa unglycosylated AQP1 in the kidney, rumen and parotid gland of all three genotypes, 40-kDa glycosylated AQP1 in renal cortex and medulla. (2) Yaks expressed less 28-kDa AQP1 protein in the outer cortex (P < 0.05), significantly more in the outer medulla (P < 0.01), and slightly more in the ventral rumen (P = 0.088) than did cattle. No difference was observed in the dorsal rumen and parotid gland (P > 0.10). In conclusion, the present study is the first to confirm the presence of AQP1 in bovine rumen and parotid gland and identified its expression in yaks. Abundance of AQP1 protein in yak kidney showed some difference from indigenous cattle. This could provide a new perspective to explain some adaptive mechanisms of yaks to the harsh environment in the Qinghai–Tibetan Plateau.
Additional keywords: AQP-1, bovine, kidney, parotid gland, rumen.
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