View source for Insulin-like growth factor 2 receptor

{{about|the cation-independent mannose 6-phosphate receptor|the cation-dependent receptor|cation-dependent mannose-6-phosphate receptor}}
{{Infobox_gene}}

'''Insulin-like growth factor 2 receptor''' ('''IGF2R'''), also called the '''cation-independent mannose-6-phosphate receptor''' ('''CI-MPR''') is a [[protein]] that in humans is encoded by the ''IGF2R'' [[gene]].<ref name="pmid2963003">{{cite journal |vauthors=Oshima A, Nolan CM, Kyle JW, Grubb JH, Sly WS | title = The human cation-independent mannose 6-phosphate receptor. Cloning and sequence of the full-length cDNA and expression of functional receptor in COS cells | journal = J. Biol. Chem. | volume = 263 | issue = 5 | pages = 2553–62 | date = February 1988 | pmid = 2963003 | doi =  | url =  }}</ref><ref name="pmid2852162">{{cite journal |vauthors=Laureys G, Barton DE, Ullrich A, Francke U | title = Chromosomal mapping of the gene for the type II insulin-like growth factor receptor/cation-independent mannose 6-phosphate receptor in man and mouse | journal = Genomics | volume = 3 | issue = 3 | pages = 224–9 | date = October 1988 | pmid = 2852162 | doi = 10.1016/0888-7543(88)90083-3 | url =  }}</ref> IGF2R is a multifunctional protein [[receptor (biochemistry)|receptor]] that binds [[insulin-like growth factor 2]] (IGF2) at the [[plasma membrane|cell surface]] and [[mannose-6-phosphate]] (M6P)-tagged proteins in the ''trans''-[[Golgi apparatus|Golgi network]].<ref name="pmid2852162"/>

== Structure ==

The structure of the IGF2R is a type I transmembrane protein (that is, it has a single transmembrane domain with its [[C-terminus]] on the [[cytoplasm]]ic side of [[lipid bilayer|lipid membrane]]s) with a large extracellular/lumenal domain and a relatively short cytoplasmic tail.<ref name="pmid12612639"/> The extracellular domain consists of a small region homologous to the [[collagen]]-binding domain of [[fibronectin]] and of fifteen repeats of approximately 147 [[amino acid]] residues. Each of these repeats is homologous to the 157-residue extracytoplasmic domain of the [[mannose 6-phosphate receptor]]. Binding to IGF2 is mediated through one of the repeats, while two different repeats are responsible for binding to mannose-6-phosphate. The IGF2R is approximately 300 [[kiloDalton|kDa]] in size; it appears to exist and function as a [[protein dimer|dimer]].

== Function ==

IGF2R functions to clear IGF2 from the cell surface to attenuate signalling, and to transport lysosomal [[acid hydrolase]] precursors from the Golgi apparatus to the [[lysosome]]. After binding IGF2 at the cell surface, IGF2Rs accumulate in forming [[clathrin]]-coated [[vesicle (biology)|vesicles]] and are [[endocytosis|internalized]]. In the [[Lumen (anatomy)|lumen]] of the ''trans''-Golgi network, the IGF2R binds M6P-tagged cargo.<ref name="pmid12612639">{{cite journal |vauthors=Ghosh P, Dahms NM, Kornfeld S | title = Mannose 6-phosphate receptors: new twists in the tale | journal = Nat. Rev. Mol. Cell Biol. | volume = 4 | issue = 3 | pages = 202–12 | date = March 2003 | pmid = 12612639 | doi = 10.1038/nrm1050 | url =  }}</ref> The IGF2Rs (bound to their cargo) are recognized by the [[GGA1|GGA]] family of [[clathrin]] adaptor proteins and accumulate in forming clathrin-coated vesicles.<ref name="pmid15511083">{{cite journal |vauthors=Ghosh P, Kornfeld S | title = The GGA proteins: key players in protein sorting at the trans-Golgi network | journal = Eur. J. Cell Biol. | volume = 83 | issue = 6 | pages = 257–62 | date = July 2004 | pmid = 15511083 | doi = 10.1078/0171-9335-00374 | url =  }}</ref> IGF2Rs from both the cell surface and the Golgi are trafficked to the early [[endosome]] where, in the relatively low [[pH]] environment of the endosome, the IGF2Rs release their cargo. The IGF2Rs are recycled back to the Golgi by the [[retromer]] complex, again by way of interaction with GGAs and vesicles. The cargo proteins are then trafficked to the lysosome via the late endosome independently of the IGF2Rs.

== Interactions ==

Insulin-like growth factor 2 receptor has been shown to [[Protein-protein interaction|interact]] with [[M6PRBP1]].<ref name="pmid9590177">{{cite journal |vauthors=Díaz E, Pfeffer SR | title = TIP47: a cargo selection device for mannose 6-phosphate receptor trafficking | journal = Cell | volume = 93 | issue = 3 | pages = 433–43 | date = May 1998 | pmid = 9590177 | doi = 10.1016/S0092-8674(00)81171-X | url =  }}</ref><ref name="pmid10908666">{{cite journal |vauthors=Orsel JG, Sincock PM, Krise JP, Pfeffer SR | title = Recognition of the 300-kDa mannose 6-phosphate receptor cytoplasmic domain by 47-kDa tail-interacting protein | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 97 | issue = 16 | pages = 9047–51 | date = August 2000 | pmid = 10908666 | pmc = 16819 | doi = 10.1073/pnas.160251397 | url =  }}</ref>

== Evolution ==

The insulin-like growth factor 2 receptor function evolved from the cation-independent mannose 6-phosphate receptor and is first seen in Monotremes. The IGF-2 binding site was likely acquired fortuitously with the generation of an exonic splice site enhancer cluster in exon 34, presumably necessitated by several kilobases of repeat element insertions in the preceding intron. A six-fold affinity maturation then followed during therian evolution, coincident with the onset of imprinting and consistent with the theory of parental conflict.<ref name="PMID 23197533 ">{{cite journal |vauthors=Williams C, Hoppe HJ, Rezgui D, Strickland M, Forbes BE, Grutzner F, Frago S, Ellis RZ, Wattana-Amorn P, Prince SN, Zaccheo OJ, Nolan CM, Mungall AJ, Jones EY, Crump MP, Hassan AB | title = Exon splice enhancer primes IGF2:IGF2R binding site structure and function evolution | journal = Science | volume = 338 | issue = 6111 | pages = 1209–1213 | date = November 2012 | pmid = 23197533 | doi = 10.1126/science.1228633 | pmc=4658703}}</ref>

==See also==
* [[Cluster of differentiation]]
* [[IGF-1 Receptor]]
* [[Mannose 6-phosphate receptor]]

== References ==
{{Reflist|35em}}

== Further reading ==
{{refbegin|35em}}
*{{cite journal |vauthors=O'Dell SD, Day IN | title = Insulin-like growth factor II (IGF-II) | journal = Int. J. Biochem. Cell Biol. | volume = 30 | issue = 7 | pages = 767–71 | year = 1998 | pmid = 9722981 | doi = 10.1016/S1357-2725(98)00048-X }}
*{{cite journal |vauthors=Hawkes C, Kar S | title = The insulin-like growth factor-II/mannose-6-phosphate receptor: structure, distribution and function in the central nervous system | journal = Brain Res. Brain Res. Rev. | volume = 44 | issue = 2–3 | pages = 117–40 | year = 2004 | pmid = 15003389 | doi = 10.1016/j.brainresrev.2003.11.002 }}
*{{cite journal |vauthors=Scott CD, Firth SM | title = The role of the M6P/IGF-II receptor in cancer: tumor suppression or garbage disposal? | journal = Horm. Metab. Res. | volume = 36 | issue = 5 | pages = 261–71 | year = 2005 | pmid = 15156403 | doi = 10.1055/s-2004-814477 }}
*{{cite journal |vauthors=Antoniades HN, Galanopoulos T, Neville-Golden J, Maxwell M | title = Expression of insulin-like growth factors I and II and their receptor mRNAs in primary human astrocytomas and meningiomas; in vivo studies using in situ hybridization and immunocytochemistry | journal = Int. J. Cancer | volume = 50 | issue = 2 | pages = 215–22 | year = 1992 | pmid = 1370435 | doi = 10.1002/ijc.2910500210 }}
*{{cite journal |vauthors=Zhou J, Bondy C | title = Insulin-like growth factor-II and its binding proteins in placental development | journal = Endocrinology | volume = 131 | issue = 3 | pages = 1230–40 | year = 1992 | pmid = 1380437 | doi = 10.1210/en.131.3.1230 }}
*{{cite journal |vauthors=Morgan DO, Edman JC, Standring DN, Fried VA, Smith MC, Roth RA, Rutter WJ | title = Insulin-like growth factor II receptor as a multifunctional binding protein | journal = Nature | volume = 329 | issue = 6137 | pages = 301–7 | year = 1987 | pmid = 2957598 | doi = 10.1038/329301a0 }}
*{{cite journal |vauthors=Oshima A, Nolan CM, Kyle JW, Grubb JH, Sly WS | title = The human cation-independent mannose 6-phosphate receptor. Cloning and sequence of the full-length cDNA and expression of functional receptor in COS cells | journal = J. Biol. Chem. | volume = 263 | issue = 5 | pages = 2553–62 | year = 1988 | pmid = 2963003 | doi =  }}
*{{cite journal |vauthors=De Souza AT, Hankins GR, Washington MK, Orton TC, Jirtle RL | title = M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity | journal = Nat. Genet. | volume = 11 | issue = 4 | pages = 447–9 | year = 1996 | pmid = 7493029 | doi = 10.1038/ng1295-447 }}
*{{cite journal |vauthors=Ilvesmäki V, Blum WF, Voutilainen R | title = Insulin-like growth factor binding proteins in the human adrenal gland | journal = Mol. Cell. Endocrinol. | volume = 97 | issue = 1–2 | pages = 71–9 | year = 1994 | pmid = 7511544 | doi = 10.1016/0303-7207(93)90212-3 }}
*{{cite journal |vauthors=De Souza AT, Hankins GR, Washington MK, Fine RL, Orton TC, Jirtle RL | title = Frequent loss of heterozygosity on 6q at the mannose 6-phosphate/insulin-like growth factor II receptor locus in human hepatocellular tumors | journal = Oncogene | volume = 10 | issue = 9 | pages = 1725–9 | year = 1995 | pmid = 7753549 | doi =  }}
*{{cite journal |vauthors=Schmidt B, Kiecke-Siemsen C, Waheed A, Braulke T, von Figura K | title = Localization of the insulin-like growth factor II binding site to amino acids 1508-1566 in repeat 11 of the mannose 6-phosphate/insulin-like growth factor II receptor | journal = J. Biol. Chem. | volume = 270 | issue = 25 | pages = 14975–82 | year = 1995 | pmid = 7797478 | doi = 10.1074/jbc.270.25.14975 }}
*{{cite journal |vauthors=Rao PH, Murty VV, Gaidano G, Hauptschein R, Dalla-Favera R, Chaganti RS | title = Subregional mapping of 8 single copy loci to chromosome 6 by fluorescence in situ hybridization | journal = Cytogenet. Cell Genet. | volume = 66 | issue = 4 | pages = 272–3 | year = 1994 | pmid = 8162705 | doi = 10.1159/000133710 }}
*{{cite journal |vauthors=Ishiwata T, Bergmann U, Kornmann M, Lopez M, Beger HG, Korc M | title = Altered expression of insulin-like growth factor II receptor in human pancreatic cancer | journal = Pancreas | volume = 15 | issue = 4 | pages = 367–73 | year = 1997 | pmid = 9361090 | doi = 10.1097/00006676-199711000-00006 }}
*{{cite journal |vauthors=Tikkanen R, Peltola M, Oinonen C, Rouvinen J, Peltonen L | title = Several cooperating binding sites mediate the interaction of a lysosomal enzyme with phosphotransferase | journal = EMBO J. | volume = 16 | issue = 22 | pages = 6684–93 | year = 1998 | pmid = 9362483 | pmc = 1170273 | doi = 10.1093/emboj/16.22.6684 }}
*{{cite journal |vauthors=Nykjaer A, Christensen EI, Vorum H, Hager H, Petersen CM, Røigaard H, Min HY, Vilhardt F, Møller LB, Kornfeld S, Gliemann J | title = Mannose 6-Phosphate/Insulin-like Growth Factor–II Receptor Targets the Urokinase Receptor to Lysosomes via a Novel Binding Interaction | journal = J. Cell Biol. | volume = 141 | issue = 3 | pages = 815–28 | year = 1998 | pmid = 9566979 | pmc = 2132758 | doi = 10.1083/jcb.141.3.815 }}
*{{cite journal |vauthors=Díaz E, Pfeffer SR | title = TIP47: a cargo selection device for mannose 6-phosphate receptor trafficking | journal = Cell | volume = 93 | issue = 3 | pages = 433–43 | year = 1998 | pmid = 9590177 | doi = 10.1016/S0092-8674(00)81171-X }}
*{{cite journal |vauthors=Wan L, Molloy SS, Thomas L, Liu G, Xiang Y, Rybak SL, Thomas G | title = PACS-1 defines a novel gene family of cytosolic sorting proteins required for trans-Golgi network localization | journal = Cell | volume = 94 | issue = 2 | pages = 205–16 | year = 1998 | pmid = 9695949 | doi = 10.1016/S0092-8674(00)81420-8 }}
*{{cite journal |vauthors=Killian JK, Jirtle RL | title = Genomic structure of the human M6P/IGF2 receptor | journal = Mamm. Genome | volume = 10 | issue = 1 | pages = 74–7 | year = 1999 | pmid = 9892739 | doi = 10.1007/s003359900947 }}
*{{cite journal |vauthors=Kumar S, Hand AT, Connor JR, Dodds RA, Ryan PJ, Trill JJ, Fisher SM, Nuttall ME, Lipshutz DB, Zou C, Hwang SM, Votta BJ, James IE, Rieman DJ, Gowen M, Lee JC | title = Identification and cloning of a connective tissue growth factor-like cDNA from human osteoblasts encoding a novel regulator of osteoblast functions | journal = J. Biol. Chem. | volume = 274 | issue = 24 | pages = 17123–31 | year = 1999 | pmid = 10358067 | doi = 10.1074/jbc.274.24.17123 }}
{{refend}}

==External links==
* {{MeshName|Insulin-Like-Growth-Factor+II+Receptor}}

{{PDB Gallery|geneid=3482}}
{{Clusters of differentiation}}
{{Growth factor receptors}}
{{Growth factor receptor modulators}}

[[Category:Receptors]]
[[Category:Clusters of differentiation]]