Cloning and expression analysis of a muscarinic cholinergic receptor from the brain of ant,Polyrhachis vicina |
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Authors: | Shu‐Min Lü Zhuo Zhao Ke Li Ya‐Lin Zhang Geng‐Si Xi |
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Affiliation: | 1. Key Laboratory of Plant Protection Resources and Pest Management, National Ministry Education, Northwest A&F Universtiy, Yangling, Shaanxi, People's Republic of China;2. College of Life Science, Jilin Normal University, Siping, Jilin, People's Republic of China;3. College of Life Science, Shaanxi Normal University, Xi'an, Shaanxi, People's Republic of China;4. College of Life Science, Shanxi Normal University, Linfen, People's Republic of China |
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Abstract: | ![]() Muscarinic acetylcholine receptors (mAchRs) are the predominant cholinergic receptors in the central and peripheral nervous systems of animals. They also have been found in various insect nervous systems. In this article, a full‐length cDNA of a pupative mAchR (PmAchR) was obtained from the brains of ant Polyrhachis vicina by homology cloning in combination with rapid amplification of cDNA ends. PmAchR encodes a 599‐amino acid protein that exhibits a high degree of homology with other mAchRs. Real‐time quantitative RT‐PCR analysis showed that PmAchR is differentially expressed in the brains of workers, males, and females. By in situ hybridization, it is revealed that PmAchR is widely expressed in different soma clusters of the brain, including the mushroom bodies, the antennal lobes, as well as the optic lobes (OL), and the most intensely staining is found in Kenyon cells. Nonetheless, there are more positive nerve fibers in the OL of males' brains than in females' and workers' brains. © 2011 Wiley Periodicals, Inc. |
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Keywords: | muscarinic acetylcholine receptors (mAchRs) Polyrhachis vicina Real‐time quantitative RT‐PCR in situ hybridization |
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