The detection of 3 leptin receptor isoforms in crucian carp gill and the influence of fasting and hypoxia on their expression

To understand leptin signaling pathway in the crucian carp ( Carassius carassius), we cloned 3 leptin receptor isoform complementary DNAs (ie, the long form [cclpr-L], the short form [cclpr-s1], and the secreted form [cclpr-s2]). Variant cclpr-L had a 3,255-bp open reading frame and a complete intra...

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Veröffentlicht in:Domestic animal endocrinology 2011-08, Vol.41 (2), p.74-80
Hauptverfasser: Cao, Y.-B., Xue, J.L., Wu, L.-Y., Jiang, W., Hu, P.-N., Zhu, J.
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Sprache:eng
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Zusammenfassung:To understand leptin signaling pathway in the crucian carp ( Carassius carassius), we cloned 3 leptin receptor isoform complementary DNAs (ie, the long form [cclpr-L], the short form [cclpr-s1], and the secreted form [cclpr-s2]). Variant cclpr-L had a 3,255-bp open reading frame and a complete intracellular domain with box 1 and box 2 consensus sequences. By contrast, cclpr-s1 contained only 4 amino acids in its intracellular domain, without the “box 1” motif, which is conserved among membrane-bound leptin receptor short isoforms in mammals. Variant cclpr-s2 had no transmembrane domain, suggesting that it is a soluble form of the receptor, and alternative splicing of cclpr-s2 mRNA employs a different mechanism for the generation of soluble leptin receptor by intron retention. The fasting-treated fish showed significantly lower cclpr-L mRNA levels in gill tissue than the control group, whereas cclpr-s2 mRNA levels did not vary significantly among the groups. Treatment with hypoxia significantly increased mRNA levels of both cclpr-L and cclpr-s2 in gill tissue. To our knowledge, this is the first study of leptin receptor isoforms expression in teleosts.
ISSN:0739-7240
1879-0054
DOI:10.1016/j.domaniend.2011.04.002