Epsins are a family of highly conserved membrane proteins that are important in creating membrane curvature. Epsins contribute to membrane deformations like endocytosis, and block vesicle formation during mitosis.[1]

Crystal Structure of the ENTH Domain of Rattus norvegicus Epsin1

Structure

Epsin contains various protein domains that aid in function. Starting at the N-terminus is the ENTH domain. ENTH stands for Epsin N-Terminal Homolog. The ENTH domain is approximately 150 amino acids long and is highly conserved across species.[1] It is composed of seven α-helices and an eighth helix that is not aligned with the seven helices that make up a superhelical fold.[1] The role of the ENTH domain is to bind membrane lipids which is currently thought to aid in the invagination of the plasma membrane to form clathrin-coated vesicles. Additionally, located toward the C-terminus of the ENTH domain are two to three ubiquitin interacting motifs which aids in ubiquitin dependent recruitment.[1]

Following the ENTH domain there is not as much conservation in structure across species. However, in higher eukaryotes there are several conserved motifs such as the clathrin-binding motifs which bind clathrin heavy chain, these motifs flank a cluster of up to eight DP repeats which bind to AP2.

Function

In general, most vertebrates contain at least two epsin paralogs. The two paralogs, epsin-1 and epsin-2 are members that contribute to the clathrin coated endocytotic machinery and are localized at the plasma membrane.[1] In mammals, the two main classes of Epsins are expressed throughout tissues but has the highest expression in the brain, whereas the third Epsin has higher expression in the epidermis and the stomach.[2]

Clathrin Coated Vesicle Formation

Epsins have many different domains to interact with various proteins related to endocytosis. At its N-terminus is an ENTH domain that binds phosphatidylinositol (4,5)-bisphosphate, meaning that it binds a lipid of biological membranes. It has also been postulated that this is a site for cargo-binding. In the middle of the epsin sequence are two UIMs (ubiquitin-interacting motifs). The C-terminus contains multiple binding sites, for example for clathrin and AP2 adaptors. As such, epsins are able to bind to membranes with specific cargo and connect them with the endocytosis machinery, so one may understand epsins as something like Swiss army knives for endocytosis.

Epsins may be the major membrane curvature-driving proteins in many clathrin-coated vesicle budding events. In addition to its primary role as an endocytic adapter, there is evidence the epsins play a role in regulating GTPase activity which provides an alternative mechanism for epsin's role in cell polarity and migration.[2]

In addition, Epsin is thought to play a role in the Notch Signaling Pathway, which is critical for normal embryonic development. Notch Signaling is dependent on the proteolytic cleavage of the Notch receptor intracellular domain. Epsin's role in Notch Signaling is due to Notch's reliance on ligand endocytosis to release the Notch intracellular domain. This occurs through ubiquitination of the D114 notch ligand which provides a docking location of the epsin UIM domain. Current research suggest that this directing of cargo material aids in the recycling in Notch signaling as well. A study on knock out epsins 1 and 2 in mice showed embryonic death at day 10. Further investigation showed vascular defects in the embryo proper, placenta and yolk sac which are characteristic of a loss in notch signaling.[3]

Family members

There are four human genes encoding epsin family members: EPN1, EPN2, EPN3, and EPN4.

The epsin homologue of C. elegans is EPN-1. EPN-1 conserves the UIM, ENTH domain, and clathrin-binding motif.

The epsin homologue of Drosophila melanogaster is liquid facets and was first identified due to its role in eye patterning in flies.

There are three Arabidopsis thaliana genes encoding epsin family members, Epsin1, Epsin2 and Epsin3 that differ in molecular weight and C - terminal domains.[4] Epsin1 has highest expression in cotyledons and flowers while Epsin2 and Epsin3 expression is currently unknown.[5] Little is known about the role plant Epsin plays in clathrin coated vesicle formation.

Clinical significance

Epsin is thought to have role in the angiogenesis of tumors; thus, epsin has the potential to be a target for anti-cancer therapies. Several cancers including prostate, breast, lung and skin display an upregulation in epsin. Research indicates that the overexpression could affect the regulation of tumor angiogenesis through defects in the notch pathway.[2] There is also evidence that Epsin could lead to colon cancer through impaired Wnt signaling by reducing the stability of the Wnt effector dishevelled, making epsin a possible target for pharmaceuticals.[6]

Epsin 4, which encodes the protein enthoprotin, now known as clathrin interactor 1 (CLINT1), has been studied for a possible relationship to schizophrenia in four independent studies, though no conclusive evidence has been found in the analysis of SNPs believed to be associated with schizophrenia (rs1186922, rs254664, rs10046055).[7][8][9][10][11] A genetic abnormality in CLINT1 is assumed to change the way internalisation of neurotransmitter receptors occurs in the brains of people with schizophrenia.

References

  1. ^ a b c d e Sen A, Madhivanan K, Mukherjee D, Aguilar RC (Apr 2012). "The epsin protein family: coordinators of endocytosis and signaling". Biomolecular Concepts. 3 (2): 117–126. doi:10.1515/bmc-2011-0060. PMC 3431554. PMID 22942912.
  2. ^ a b c Tessneer, KL; Cai, X; Pasula, S; Dong, Y; Liu, X; Chang, B; McManus, J; Hahn, S; Yu, L; Chen, H (1 July 2013). "Epsin Family of Endocytic Adaptor Proteins as Oncogenic Regulators of Cancer Progression". Journal of Cancer Research Updates. 2 (3): 144–150. doi:10.6000/1929-2279.2013.02.03.2. PMC 3911794. PMID 24501612.
  3. ^ Musse, AA; Meloty-Kapella, L; Weinmaster, G (June 2012). "Notch ligand endocytosis: mechanistic basis of signaling activity". Seminars in Cell & Developmental Biology. 23 (4): 429–36. doi:10.1016/j.semcdb.2012.01.011. PMC 3507467. PMID 22306180.
  4. ^ Holstein, Susanne E. H.; Oliviusson, Peter (20 October 2005). "Sequence analysis of Arabidopsis thaliana E/ANTH-domain-containing proteins: membrane tethers of the clathrin-dependent vesicle budding machinery". Protoplasma. 226 (1–2): 13–21. doi:10.1007/s00709-005-0105-7.
  5. ^ Song, J. (1 September 2006). "Arabidopsis EPSIN1 Plays an Important Role in Vacuolar Trafficking of Soluble Cargo Proteins in Plant Cells via Interactions with Clathrin, AP-1, VTI11, and VSR1". The Plant Cell Online. 18 (9): 2258–2274. doi:10.1105/tpc.105.039123. PMC 1560928. PMID 16905657.
  6. ^ Chang, Baojun; Tessneer, Kandice L.; McManus, John; Liu, Xiaolei; Hahn, Scott; Pasula, Satish; Wu, Hao; Song, Hoogeun; Chen, Yiyuan; Cai, Xiaofeng; Dong, Yunzhou; Brophy, Megan L.; Rahman, Ruby; Ma, Jian-Xing; Xia, Lijun; Chen, Hong (16 March 2015). "Epsin is required for Dishevelled stability and Wnt signalling activation in colon cancer development". Nature Communications. 6: 6380. doi:10.1038/ncomms7380. PMC 4397653. PMID 25871009.
  7. ^ Pimm J, McQuillin A, Thirumalai S, Lawrence J, Quested D, Bass N, Lamb G, Moorey H, Datta SR, Kalsi G, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Curtis D, Gurling H (May 2005). "The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia". American Journal of Human Genetics. 76 (5): 902–7. doi:10.1086/430095. PMC 1199380. PMID 15793701.
  8. ^ Tang RQ, Zhao XZ, Shi YY, Tang W, Gu NF, Feng GY, Xing YL, Zhu SM, Sang H, Liang PJ, He L (Apr 2006). "Family-based association study of Epsin 4 and Schizophrenia". Molecular Psychiatry. 11 (4): 395–9. doi:10.1038/sj.mp.4001780. PMID 16402136.
  9. ^ Liou YJ, Lai IC, Wang YC, Bai YM, Lin CC, Lin CY, Chen TT, Chen JY (Jun 2006). "Genetic analysis of the human ENTH (Epsin 4) gene and schizophrenia". Schizophrenia Research. 84 (2–3): 236–43. doi:10.1016/j.schres.2006.02.021. PMID 16616458.
  10. ^ Gurling H, Pimm J, McQuillin A (Jan 2007). "Replication of genetic association studies between markers at the Epsin 4 gene locus and schizophrenia in two Han Chinese samples". Schizophrenia Research. 89 (1–3): 357–9. doi:10.1016/j.schres.2006.08.024. PMID 17070672.
  11. ^ Escamilla M, Lee BD, Ontiveros A, Raventos H, Nicolini H, Mendoza R, Jerez A, Munoz R, Medina R, Figueroa A, Walss-Bass C, Armas R, Contreras S, Ramirez ME, Dassori A (Dec 2008). "The epsin 4 gene is associated with psychotic disorders in families of Latin American origin". Schizophrenia Research. 106 (2–3): 253–7. doi:10.1016/j.schres.2008.09.005. PMID 18929466.

Further reading

  • Horvath CA, Vanden Broeck D, Boulet GA, Bogers J, De Wolf MJ (2007). "Epsin: inducing membrane curvature". The International Journal of Biochemistry & Cell Biology. 39 (10): 1765–70. doi:10.1016/j.biocel.2006.12.004. PMID 17276129.
  • Chen H, Fre S, Slepnev VI, Capua MR, Takei K, Butler MH, Di Fiore PP, De Camilli P (Aug 1998). "Epsin is an EH-domain-binding protein implicated in clathrin-mediated endocytosis". Nature. 394 (6695): 793–7. doi:10.1038/29555. PMID 9723620.
  • Chen X, Irani NG, Firml, J (2011). "Clathrin - mediated endocytosis: the gateway into plant cells". Current Opinion in Plant Biology. 14 (6): 674–682. doi:10.1016/j.pbi.2011.08.006. PMID 21945181.
  • Cai X, Pasula S, Chang B, Hahn S, McManus J, Chen H (April 2013). "Upregulation of epsin in breast cancer and critical role of epsin in promoting cancer growth and metastasis". Cancer Research. 73: 5128. doi:10.1158/1538-7445.AM2013-5128.

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