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犬降钙素受体刺激肽与降钙素/降钙素基因相关肽的基因组及表达分析

Genomic and expression analysis of canine calcitonin receptor-stimulating peptides and calcitonin/calcitonin gene-related peptide.

作者信息

Osaki Tsukasa, Katafuchi Takeshi, Minamino Naoto

机构信息

Department of Pharmacology, National Cardiovascular Center Research Institute, Suita, Osaka, Japan.

出版信息

J Biochem. 2008 Oct;144(4):419-30. doi: 10.1093/jb/mvn084. Epub 2008 Jun 16.

Abstract

Calcitonin receptor-stimulating peptides (CRSPs) are new members of the calcitonin/calcitonin gene-related peptide (CT/CGRP) family identified in pigs, dogs and other domestic animals, and CRSP-1 is an active ligand for the CT receptor (CT-R). We recently sequenced porcine CRSP genes (Crsps) and found similarity with the CT/CGRP gene (Ct/Cgrp) in sequence and genomic organization. In this study, we identified five Crsps, Crsp-1 to Crsp-5, in dogs. Crsp-1 has five exons with an exon-intron organization identical to that of porcine Crsp-1 or Crsp-2, while Crsp-2 and Crsp-3 have additional CT-2- and CT-3-coding exons like Ct/Cgrp. Crsp-2 was renamed as Ct-2/Crsp-2 because both CRSP-2 and CT-2 mRNAs were tissue-specifically expressed. Crsp-4 and Crsp-5 are presumably generated by retrotransposition. We postulate that Crsps were generated from the gene duplication of Ct/Cgrp, and gained their diversity during mammalian evolution. Among the canine CTs and CRSPs, CRSP-1, CT-1 and CT-2 are active ligands for the CT-R, but CRSP-2 and others are inactive. Canine CRSP-1 and CT-2 are expressed in the central and peripheral systems, while CT-1 is localized in the thyroid gland. These findings indicate that dogs can be used for an experimental model as analysing the physiological roles of the CT/CGRP/CRSP family.

摘要

降钙素受体刺激肽(CRSPs)是在猪、狗和其他家畜中发现的降钙素/降钙素基因相关肽(CT/CGRP)家族的新成员,CRSP-1是降钙素受体(CT-R)的活性配体。我们最近对猪的CRSP基因(Crsps)进行了测序,发现其在序列和基因组组织上与CT/CGRP基因(Ct/Cgrp)相似。在本研究中,我们在狗身上鉴定出了5种Crsps,即Crsp-1至Crsp-5。Crsp-1有5个外显子,其外显子-内含子结构与猪的Crsp-1或Crsp-2相同,而Crsp-2和Crsp-3有额外的CT-2和CT-3编码外显子,类似于Ct/Cgrp。Crsp-2被重新命名为Ct-2/Crsp-2,因为CRSP-2和CT-2的mRNA均在组织中特异性表达。Crsp-4和Crsp-5可能是通过逆转座产生的。我们推测Crsps是由Ct/Cgrp的基因复制产生的,并在哺乳动物进化过程中获得了多样性。在犬类的CTs和CRSPs中,CRSP-1、CT-1和CT-2是CT-R的活性配体,但CRSP-2及其他则无活性。犬类CRSP-1和CT-2在中枢和外周系统中表达,而CT-1定位于甲状腺。这些发现表明,狗可作为分析CT/CGRP/CRSP家族生理作用的实验模型。

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