Chauvet M T, Chauvet J, Acher R
FEBS Lett. 1983 Nov 14;163(2):257-60. doi: 10.1016/0014-5793(83)80830-8.
The vasopressin precursor is composed of 3 domains, namely vasopressin, MSEL-neurophysin and a glycopeptide. Processing occurs during axonal transport from hypothalamus to neurohypophysis from which the 3 fragments can be isolated. The glycopeptide fragment of the rat vasopressin precursor has been purified and sequenced. Despite the fact that rat MSEL-neurophysin is shortened (93 residues instead of 95 for other mammals), rat glycopeptide has 39 residues, as do the other mammalian glycopeptides, suggesting a similar processing. Fifteen substitutions are however observed when compared to ox glycopeptide. The C-terminal part of MSEL-neurophysin (residues 77-93) and the glycopeptide are encoded by the same exon and the homologies when compared with their bovine counterparts are 58% and 62% respectively. In contrast, the central part of rat MSEL-neurophysin (residues 10-76), which is encoded by a separate exon, displays 96% of homology; vasopressin and the N-terminal part of MSEL-neurophysin (residues 1-9), encoded by a third exon, are nearly invariant.
血管加压素前体由3个结构域组成,即血管加压素、MSEL-神经垂体素和一个糖肽。加工过程发生在下丘脑到神经垂体的轴突运输过程中,可从中分离出这3个片段。大鼠血管加压素前体的糖肽片段已被纯化并测序。尽管大鼠MSEL-神经垂体素缩短了(93个残基,而其他哺乳动物为95个),但大鼠糖肽有39个残基,与其他哺乳动物的糖肽相同,这表明加工过程相似。然而,与牛糖肽相比,观察到15个替换。MSEL-神经垂体素的C末端部分(第77 - 93位残基)和糖肽由同一个外显子编码,与它们的牛对应物相比,同源性分别为58%和62%。相比之下,大鼠MSEL-神经垂体素的中央部分(第10 - 76位残基)由一个单独的外显子编码,显示出96%的同源性;血管加压素和MSEL-神经垂体素的N末端部分(第1 - 9位残基)由第三个外显子编码,几乎是不变的。