Tostivint Hervé, Lihrmann Isabelle, Vaudry Hubert
INSERM U413, Laboratory of Cellular and Molecular Neuroendocrinology, University of Rouen, 76821 Mont-Saint-Aignan, France.
Mol Cell Endocrinol. 2008 May 14;286(1-2):5-17. doi: 10.1016/j.mce.2008.02.029. Epub 2008 Mar 6.
The present review describes the molecular evolution of the somatostatin family and its relationships with that of the urotensin II family. Most of the somatostatin sequences collected from different vertebrate species can be grouped as the products of at least four loci. The somatostatin 1 (SS1) gene is present in all vertebrate classes from agnathans to mammals. The SS1 gene has given rise to the somatostatin 2 (SS2) gene by a segment/chromosome duplication that is probably the result of a tetraploidization event according to the 2R hypothesis. The somatostatin-related peptide cortistatin, first identified in rodents and human, is the counterpart of SS2 in placental mammals. In fish, the existence of two additional somatostatin genes has been reported. The first gene, which encodes a peptide usually named somatostatin II (SSII), exists in almost all teleost species investigated so far and is thought to have arisen through local duplication of the SS1 gene. The second gene, which has been characterized in only a few teleost species, encodes a peptide also named SSII that exhibits a totally atypical structure. The origin of this gene is currently unknown. Nevertheless, because the two latter genes are clearly paralogous genes, we propose to rename them SS3 and SS4, respectively, in order to clarify the current confusing nomenclature. The urotensin II family consists of two genes, namely the urotensin II (UII) gene and the UII-related peptide (URP) gene. Both UII and URP exhibit limited structural identity to somatostatin so that UII was originally described as a "somatostatin-like peptide". Recent comparative genomics studies have revealed that the SS1 and URP genes, on the one hand, and the SS2 and UII genes, on the other hand, are closely linked on the same chromosomes, thus confirming that the SS1/SS2 and the UII/URP genes belong to the same superfamily. According to these data, it appears that an ancestral somatostatin/urotensin II gene gave rise by local duplication to a somatostatin ancestor and a urotensin II ancestor, whereupon this pair was duplicated (presumably by a segment/chromosome duplication) to give rise to the SS1-UII pair and the SS2-URP pair.
本综述描述了生长抑素家族的分子进化及其与尾加压素II家族的关系。从不同脊椎动物物种收集的大多数生长抑素序列可归为至少四个基因座的产物。生长抑素1(SS1)基因存在于从无颌类到哺乳动物的所有脊椎动物类别中。根据2R假说,SS1基因通过片段/染色体复制产生了生长抑素2(SS2)基因,这可能是四倍体化事件的结果。最早在啮齿动物和人类中发现的与生长抑素相关的肽可替丁,是胎盘哺乳动物中SS2的对应物。在鱼类中,已报道存在另外两个生长抑素基因。第一个基因编码一种通常称为生长抑素II(SSII)的肽,几乎存在于迄今研究的所有硬骨鱼物种中,被认为是通过SS1基因的局部复制产生的。第二个基因仅在少数硬骨鱼物种中得到表征,编码一种也称为SSII的肽,其结构完全非典型。该基因的起源目前尚不清楚。然而,由于后两个基因显然是旁系同源基因,我们建议分别将它们重新命名为SS3和SS4,以澄清当前混乱的命名法。尾加压素II家族由两个基因组成,即尾加压素II(UII)基因和UII相关肽(URP)基因。UII和URP与生长抑素的结构相似性有限,因此UII最初被描述为一种“生长抑素样肽”。最近的比较基因组学研究表明,一方面SS1和URP基因,另一方面SS2和UII基因,在同一条染色体上紧密相连,从而证实SS1/SS2和UII/URP基因属于同一超家族。根据这些数据,似乎一个祖先生长抑素/尾加压素II基因通过局部复制产生了一个生长抑素祖先和一个尾加压素II祖先,随后这一对基因被复制(可能通过片段/染色体复制),产生了SS1-UII对和SS2-URP对。