{"title":"果蝇TGF-β家族信号传导","authors":"George Pyrowolakis, B. Hartmann, M. Affolter","doi":"10.1101/087969752.50.493","DOIUrl":null,"url":null,"abstract":"In this chapter, we first introduce the general components of the different transforming growth factor-β (TGF-β) family signaling pathways that have been identified in Drosophila . We then describe at which steps and how the signaling pathways are regulated at different developmental stages. We highlight two topics—extracellular ligand distribution and nuclear readout of distinct levels of signaling—in which Drosophila work has provided unique insight in the past decade. For several reviews that discuss other aspects of TGF-β family signaling in Drosophila in more detail, see Affolter et al. (2001), Parker et al. (2004), and Raftery and Sutherland (1999). CORE EFFECTORS OF THE TGF-β FAMILY SIGNALING PATHWAYS IN DROSOPHILA The core components of TGF-β family signaling pathways in Drosophila show a high degree of conservation at the sequence as well as at the functional level with regard to their vertebrate counterparts, that is, the bone morphogenetic protein- (BMP) and activin-signaling pathways. In fact, several genes encoding Drosophila TGF-β family ligands or receptors were identified using polymerase chain reaction (PCR) approaches or by DNA sequence data mining starting from the sequences for mammalian members of the signaling pathway. The number of ligands and receptors encoded by the Drosophila genome is lower than that in vertebrates; seven ligand and five receptor-encoding genes have been identified (Fig. 1) (Parker et al. 2004). Three of the seven ligands, Decapentaplegic (Dpp), Screw (Scw), and Glass bottom boat (Gbb; formerly termed 60A), belong to the subfamily of BMPs, whereas dActivin and Dawdle (Daw) are related to...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"63 1","pages":"493-526"},"PeriodicalIF":0.0000,"publicationDate":"2008-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"17 TGF-β Family Signaling in Drosophila\",\"authors\":\"George Pyrowolakis, B. Hartmann, M. Affolter\",\"doi\":\"10.1101/087969752.50.493\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this chapter, we first introduce the general components of the different transforming growth factor-β (TGF-β) family signaling pathways that have been identified in Drosophila . We then describe at which steps and how the signaling pathways are regulated at different developmental stages. We highlight two topics—extracellular ligand distribution and nuclear readout of distinct levels of signaling—in which Drosophila work has provided unique insight in the past decade. For several reviews that discuss other aspects of TGF-β family signaling in Drosophila in more detail, see Affolter et al. (2001), Parker et al. (2004), and Raftery and Sutherland (1999). CORE EFFECTORS OF THE TGF-β FAMILY SIGNALING PATHWAYS IN DROSOPHILA The core components of TGF-β family signaling pathways in Drosophila show a high degree of conservation at the sequence as well as at the functional level with regard to their vertebrate counterparts, that is, the bone morphogenetic protein- (BMP) and activin-signaling pathways. In fact, several genes encoding Drosophila TGF-β family ligands or receptors were identified using polymerase chain reaction (PCR) approaches or by DNA sequence data mining starting from the sequences for mammalian members of the signaling pathway. The number of ligands and receptors encoded by the Drosophila genome is lower than that in vertebrates; seven ligand and five receptor-encoding genes have been identified (Fig. 1) (Parker et al. 2004). Three of the seven ligands, Decapentaplegic (Dpp), Screw (Scw), and Glass bottom boat (Gbb; formerly termed 60A), belong to the subfamily of BMPs, whereas dActivin and Dawdle (Daw) are related to...\",\"PeriodicalId\":10493,\"journal\":{\"name\":\"Cold Spring Harbor Monograph Archive\",\"volume\":\"63 1\",\"pages\":\"493-526\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cold Spring Harbor Monograph Archive\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/087969752.50.493\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969752.50.493","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
在本章中,我们首先介绍了在果蝇中发现的不同转化生长因子-β (TGF-β)家族信号通路的一般成分。然后,我们描述了在哪些步骤和如何在不同的发育阶段调节信号通路。我们强调两个主题-细胞外配体分布和不同水平信号的核读出-在果蝇的工作中提供了独特的见解在过去的十年中。关于更详细地讨论果蝇中TGF-β家族信号传导的其他方面的几篇综述,请参见Affolter et al.(2001)、Parker et al.(2004)和ratry and Sutherland(1999)。果蝇TGF-β家族信号通路的核心效应因子果蝇TGF-β家族信号通路的核心成分在序列和功能水平上与脊椎动物的对应体骨形态发生蛋白(BMP)和激活素信号通路具有高度的保守性。事实上,利用聚合酶链反应(PCR)方法或从哺乳动物信号通路成员序列开始的DNA序列数据挖掘,已经鉴定出了几个编码果蝇TGF-β家族配体或受体的基因。果蝇基因组编码的配体和受体数量低于脊椎动物;已经鉴定出7个配体和5个受体编码基因(图1)(Parker et al. 2004)。七种配体中的三种,Decapentaplegic (Dpp)、Screw (Scw)和Glass bottom boat (Gbb);以前称为60A),属于bmp亚家族,而dActivin和Dawdle (Daw)与…
In this chapter, we first introduce the general components of the different transforming growth factor-β (TGF-β) family signaling pathways that have been identified in Drosophila . We then describe at which steps and how the signaling pathways are regulated at different developmental stages. We highlight two topics—extracellular ligand distribution and nuclear readout of distinct levels of signaling—in which Drosophila work has provided unique insight in the past decade. For several reviews that discuss other aspects of TGF-β family signaling in Drosophila in more detail, see Affolter et al. (2001), Parker et al. (2004), and Raftery and Sutherland (1999). CORE EFFECTORS OF THE TGF-β FAMILY SIGNALING PATHWAYS IN DROSOPHILA The core components of TGF-β family signaling pathways in Drosophila show a high degree of conservation at the sequence as well as at the functional level with regard to their vertebrate counterparts, that is, the bone morphogenetic protein- (BMP) and activin-signaling pathways. In fact, several genes encoding Drosophila TGF-β family ligands or receptors were identified using polymerase chain reaction (PCR) approaches or by DNA sequence data mining starting from the sequences for mammalian members of the signaling pathway. The number of ligands and receptors encoded by the Drosophila genome is lower than that in vertebrates; seven ligand and five receptor-encoding genes have been identified (Fig. 1) (Parker et al. 2004). Three of the seven ligands, Decapentaplegic (Dpp), Screw (Scw), and Glass bottom boat (Gbb; formerly termed 60A), belong to the subfamily of BMPs, whereas dActivin and Dawdle (Daw) are related to...