Rucinski Marcin, Malendowicz Ludwik K
Department of Histology and Embryology, Unversity of Medical Sciences, Poznan, PL-60781, Poland.
Int J Mol Med. 2009 Jan;23(1):113-9.
The hexadecapeptide cerebellin (CER) is derived from a larger protein, cerebellin 1 precursor protein (Cbln1). At present four precerebellins (Cbln1-4) are known. They are highly expressed in the brain, in particular in the cerebellum. Since CER is involved in regulating endocrine functions, present studies aimed to investigate, by means of molecular biology techniques (RT-PCR, QPCR, Western blotting) the expression of Cbln related genes and Cbln1 protein in classic endocrine glands of the rat. RT-PCR revealed the presence of Cbln1 and Cbln3 mRNAs in all endocrine glands tested; hypothalamus, anterior pituitary, thyroid, adrenal cortex, testis, ovary and pancreatic islets. Expression of Cbln2 gene was demonstrated only in the hypothalamus, anterior pituitary and adrenal cortex and in cerebral cortex, which was studied as a positive control organ. On the contrary, expression of Cbln4 gene was found only in the cerebral cortex. Using QPCR, the highest expression of Cbln1 gene was demonstrated in hypothalamus and pancreatic islets, a somewhat lower one in the anterior pituitary and thyroid, while the lowest was in adrenal cortex, testis and ovary. In general, the Cbln3 gene exhibited a similar pattern of expression, with the highest level in pancreatic islets and somewhat lower in the hypothalamus. Cbln2 gene expression was high in the hypothalamus, lower in the anterior pituitary and very low in adrenal cortex. In general, the pattern of Cbln1 protein expression was similar to that of Cbln1 mRNA. Further experiments aimed to check possible association of Cbln1 with cell membrane. Such association is suggested by differences in Cbln1 protein amount after extraction with RIPA and TRIS buffers. Bioinformatic methods predicting transmembrane topology (HMMTOP and SPLIT 4.0 servers) suggest transmembrane localisation of Cbln1, with transmembrane domain sequence responsible for the formation of an alpha-helix. These findings suggest possible physiological roles of Cbln related peptides not only in the cerebellum, but also in the endocrine system. However, their specific role as modulators of the endocrine system requires further investigations.
十六肽小脑素(CER)来源于一种更大的蛋白质,即小脑素1前体蛋白(Cbln1)。目前已知四种前小脑素(Cbln1 - 4)。它们在大脑中高度表达,尤其是在小脑中。由于CER参与调节内分泌功能,目前的研究旨在通过分子生物学技术(逆转录聚合酶链反应、定量聚合酶链反应、蛋白质免疫印迹法)研究大鼠经典内分泌腺中Cbln相关基因和Cbln1蛋白的表达。逆转录聚合酶链反应显示,在所检测的所有内分泌腺中均存在Cbln1和Cbln3信使核糖核酸;下丘脑、垂体前叶、甲状腺、肾上腺皮质、睾丸、卵巢和胰岛。Cbln2基因仅在下丘脑、垂体前叶、肾上腺皮质以及作为阳性对照器官的大脑皮质中表达。相反,Cbln4基因仅在大脑皮质中被发现。使用定量聚合酶链反应,Cbln1基因在下丘脑和胰岛中表达最高,在垂体前叶和甲状腺中略低,而在肾上腺皮质、睾丸和卵巢中最低。总体而言,则Cbln3基因呈现出类似的表达模式,在胰岛中水平最高,在下丘脑中略低。Cbln2基因在下丘脑中表达较高,在垂体前叶中较低,在肾上腺皮质中极低。总体而言,Cbln1蛋白的表达模式与Cbln1信使核糖核酸的相似。进一步的实验旨在检查Cbln1与细胞膜的可能关联。用RIPA和TRIS缓冲液提取后Cbln1蛋白量的差异提示了这种关联。预测跨膜拓扑结构的生物信息学方法(HMMTOP和SPLIT 4.0服务器)表明Cbln1具有跨膜定位,其跨膜结构域序列负责形成α - 螺旋。这些发现表明Cbln相关肽不仅在小脑中,而且在内分泌系统中可能具有生理作用。然而,它们作为内分泌系统调节剂的具体作用还需要进一步研究。