Evolution of the vertebrate insulin receptor substrate (Irs) gene family

被引:23
作者
Al-Salam, Ahmad [1 ]
Irwin, David M. [1 ,2 ]
机构
[1] Univ Toronto, Dept Lab Med & Pathobiol, Fac Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Banting & Best Diabet Ctr, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Insulin receptor substrate; Gene duplication; Protein evolution; Episodic evolution; Phylogeny; Vertebrate; Pseudogene; WHOLE-GENOME DUPLICATION; SIGNAL-TRANSDUCTION; PHOSPHOTYROSINE PROTEIN; PLECKSTRIN HOMOLOGY; WEB SERVER; SEQUENCE; GROWTH; EXPRESSION; INSIGHTS; MICE;
D O I
10.1186/s12862-017-0994-z
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Insulin receptor substrate (Irs) proteins are essential for insulin signaling as they allow downstream effectors to dock with, and be activated by, the insulin receptor. A family of four Irs proteins have been identified in mice, however the gene for one of these, IRS3, has been pseudogenized in humans. While it is known that the Irs gene family originated in vertebrates, it is not known when it originated and which members are most closely related to each other. A better understanding of the evolution of Irs genes and proteins should provide insight into the regulation of metabolism by insulin. Results: Multiple genes for Irs proteins were identified in a wide variety of vertebrate species. Phylogenetic and genomic neighborhood analyses indicate that this gene family originated very early in vertebrae evolution. Most Irs genes were duplicated and retained in fish after the fish-specific genome duplication. Irs genes have been lost of various lineages, including Irs3 in primates and birds and Irs1 in most fish. Irs3 and Irs4 experienced an episode of more rapid protein sequence evolution on the ancestral mammalian lineage. Comparisons of the conservation of the proteins sequences among Irs paralogs show that domains involved in binding to the plasma membrane and insulin receptors are most strongly conserved, while divergence has occurred in sequences involved in interacting with downstream effector proteins. Conclusions: The Irs gene family originated very early in vertebrate evolution, likely through genome duplications, and in parallel with duplications of other components of the insulin signaling pathway, including insulin and the insulin receptor. While the N-terminal sequences of these proteins are conserved among the paralogs, changes in the C-terminal sequences likely allowed changes in biological function.
引用
收藏
页数:14
相关论文
共 81 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   ALTERNATIVE PATHWAY OF INSULIN SIGNALING IN MICE WITH TARGETED DISRUPTION OF THE IRS-1 GENE [J].
ARAKI, E ;
LIPES, MA ;
PATTI, ME ;
BRUNING, JC ;
HAAG, B ;
JOHNSON, RS ;
KAHN, CR .
NATURE, 1994, 372 (6502) :186-190
[3]   Role of phosphatidylinositol 3-kinase activation on insulin action and its alteration in diabetic conditions [J].
Asano, Tomoichiro ;
Fujishiro, Midorl ;
Kushiyama, Akifumi ;
Nakatsu, Yusuke ;
Yoneda, Masayasu ;
Kamata, Hideaki ;
Sakoda, Hideyuki .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2007, 30 (09) :1610-1616
[4]  
Ayres DL, 2012, SYST BIOL, V61, P170, DOI [10.1093/sysbio/syr100, 10.1093/sysbio/sys029]
[5]   Absence of functional insulin receptor substrate-3 (IRS-3) gene in humans [J].
Björnholm, M ;
He, AR ;
Attersand, A ;
Lake, S ;
Liu, SCH ;
Lienhard, GE ;
Taylor, S ;
Arner, P ;
Zierath, JR .
DIABETOLOGIA, 2002, 45 (12) :1697-1702
[6]   Sequence and structure-based prediction of eukaryotic protein phosphorylation sites [J].
Blom, N ;
Gammeltoft, S ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (05) :1351-1362
[7]   Autonomous control of cell and organ size by CHICO, a Drosophila homolog of vertebrate IRS1-4 [J].
Böhni, R ;
Riesgo-Escovar, J ;
Oldham, S ;
Brogiolo, W ;
Stocker, H ;
Andruss, BF ;
Beckingham, K ;
Hafen, E .
CELL, 1999, 97 (07) :865-875
[8]   The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons [J].
Braasch, Ingo ;
Gehrke, Andrew R. ;
Smith, Jeramiah J. ;
Kawasaki, Kazuhiko ;
Manousaki, Tereza ;
Pasquier, Jeremy ;
Amores, Angel ;
Desvignes, Thomas ;
Batzel, Peter ;
Catchen, Julian ;
Berlin, Aaron M. ;
Campbell, Michael S. ;
Barrell, Daniel ;
Martin, Kyle J. ;
Mulley, John F. ;
Ravi, Vydianathan ;
Lee, Alison P. ;
Nakamura, Tetsuya ;
Chalopin, Domitille ;
Fan, Shaohua ;
Wcisel, Dustin ;
Canestro, Cristian ;
Sydes, Jason ;
Beaudry, Felix E. G. ;
Sun, Yi ;
Hertel, Jana ;
Beam, Michael J. ;
Fasold, Mario ;
Ishiyama, Mikio ;
Johnson, Jeremy ;
Kehr, Steffi ;
Lara, Marcia ;
Letaw, John H. ;
Litman, Gary W. ;
Litman, Ronda T. ;
Mikami, Masato ;
Ota, Tatsuya ;
Saha, Nil Ratan ;
Williams, Louise ;
Stadler, Peter F. ;
Wang, Han ;
Taylor, John S. ;
Fontenot, Quenton ;
Ferrara, Allyse ;
Searle, Stephen M. J. ;
Aken, Bronwen ;
Yandell, Mark ;
Schneider, Igor ;
Yoder, Jeffrey A. ;
Volff, Jean-Nicolas .
NATURE GENETICS, 2016, 48 (04) :427-+
[9]   Docking proteins [J].
Brummer, Tilman ;
Schmitz-Peiffer, Carsten ;
Daly, Roger J. .
FEBS JOURNAL, 2010, 277 (21) :4356-4369
[10]   Ultrafast Approximation for Phylogenetic Bootstrap [J].
Bui Quang Minh ;
Minh Anh Thi Nguyen ;
von Haeseler, Arndt .
MOLECULAR BIOLOGY AND EVOLUTION, 2013, 30 (05) :1188-1195