From Wikipedia, the free encyclopedia

Exocyst complex component 3-like 2 is a protein that in humans is encoded by the EXOC3L2 gene. [1] [2] [3] [4]

The EXOC3L2 protein has been shown to interact with EXOC4 [1] that is a component of the exocyst complex [5] [6] involved exocytosis and more specifically in the targeting of exocytic vesicles to the cell membrane.

The exocyst complex is important for several biological processes, such as the establishment of cell polarity and regulation of cell migration. [5] [7] The structure and functions of the exocyst complex are conserved from yeast to higher eukaryotes. [5] [6] Endothelial cells in blood vessels express high levels of EXOC3L2 that is required for proper VEGFR-2 [1] signaling so that the endothelial cells can migrate towards the growth factor VEGF-A. [8]

References

  1. ^ a b c Barkefors, I; Fuchs, PF; Heldin, J; Bergström, T; Forsberg-Nilsson, K; Kreuger, J (2011). "Exocyst complex component 3-like 2 (EXOC3L2) associates with the exocyst complex and mediates directional migration of endothelial cells". The Journal of Biological Chemistry. 286 (27): 24189–99. doi: 10.1074/jbc.M110.212209. PMC  3129200. PMID  21566143.
  2. ^ EntrezGene 90332
  3. ^ Olgiati, P; Politis, AM; Papadimitriou, GN; De Ronchi, D; Serretti, A (2011). "Genetics of late-onset Alzheimer's disease: Update from the alzgene database and analysis of shared pathways". International Journal of Alzheimer's Disease. 2011: 832379. doi: 10.4061/2011/832379. PMC  3235576. PMID  22191060.
  4. ^ Belbin, O; Carrasquillo, MM; Crump, M; Culley, OJ; Hunter, TA; Ma, L; Bisceglio, G; Zou, F; Allen, M (2011). "Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease". Human Genetics. 129 (3): 273–82. doi: 10.1007/s00439-010-0924-2. PMC  3036835. PMID  21132329.
  5. ^ a b c Liu, J; Guo, W (2011). "The exocyst complex in exocytosis and cell migration". Protoplasma. 249 (3): 587–597. doi: 10.1007/s00709-011-0330-1. PMID  21997494. S2CID  11946932.
  6. ^ a b Munson, M; Novick, P (2006). "The exocyst defrocked, a framework of rods revealed". Nature Structural & Molecular Biology. 13 (7): 577–81. doi: 10.1038/nsmb1097. PMID  16826234. S2CID  26645238.
  7. ^ Thapa, N; Sun, Y; Schramp, M; Choi, S; Ling, K; Anderson, RA (2012). "Phosphoinositide signaling regulates the exocyst complex and polarized integrin trafficking in directionally migrating cells". Developmental Cell. 22 (1): 116–30. doi: 10.1016/j.devcel.2011.10.030. PMC  3266520. PMID  22264730.
  8. ^ Carmeliet, P; Jain, RK (2011). "Molecular mechanisms and clinical applications of angiogenesis". Nature. 473 (7347): 298–307. Bibcode: 2011Natur.473..298C. doi: 10.1038/nature10144. PMC  4049445. PMID  21593862.
From Wikipedia, the free encyclopedia

Exocyst complex component 3-like 2 is a protein that in humans is encoded by the EXOC3L2 gene. [1] [2] [3] [4]

The EXOC3L2 protein has been shown to interact with EXOC4 [1] that is a component of the exocyst complex [5] [6] involved exocytosis and more specifically in the targeting of exocytic vesicles to the cell membrane.

The exocyst complex is important for several biological processes, such as the establishment of cell polarity and regulation of cell migration. [5] [7] The structure and functions of the exocyst complex are conserved from yeast to higher eukaryotes. [5] [6] Endothelial cells in blood vessels express high levels of EXOC3L2 that is required for proper VEGFR-2 [1] signaling so that the endothelial cells can migrate towards the growth factor VEGF-A. [8]

References

  1. ^ a b c Barkefors, I; Fuchs, PF; Heldin, J; Bergström, T; Forsberg-Nilsson, K; Kreuger, J (2011). "Exocyst complex component 3-like 2 (EXOC3L2) associates with the exocyst complex and mediates directional migration of endothelial cells". The Journal of Biological Chemistry. 286 (27): 24189–99. doi: 10.1074/jbc.M110.212209. PMC  3129200. PMID  21566143.
  2. ^ EntrezGene 90332
  3. ^ Olgiati, P; Politis, AM; Papadimitriou, GN; De Ronchi, D; Serretti, A (2011). "Genetics of late-onset Alzheimer's disease: Update from the alzgene database and analysis of shared pathways". International Journal of Alzheimer's Disease. 2011: 832379. doi: 10.4061/2011/832379. PMC  3235576. PMID  22191060.
  4. ^ Belbin, O; Carrasquillo, MM; Crump, M; Culley, OJ; Hunter, TA; Ma, L; Bisceglio, G; Zou, F; Allen, M (2011). "Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease". Human Genetics. 129 (3): 273–82. doi: 10.1007/s00439-010-0924-2. PMC  3036835. PMID  21132329.
  5. ^ a b c Liu, J; Guo, W (2011). "The exocyst complex in exocytosis and cell migration". Protoplasma. 249 (3): 587–597. doi: 10.1007/s00709-011-0330-1. PMID  21997494. S2CID  11946932.
  6. ^ a b Munson, M; Novick, P (2006). "The exocyst defrocked, a framework of rods revealed". Nature Structural & Molecular Biology. 13 (7): 577–81. doi: 10.1038/nsmb1097. PMID  16826234. S2CID  26645238.
  7. ^ Thapa, N; Sun, Y; Schramp, M; Choi, S; Ling, K; Anderson, RA (2012). "Phosphoinositide signaling regulates the exocyst complex and polarized integrin trafficking in directionally migrating cells". Developmental Cell. 22 (1): 116–30. doi: 10.1016/j.devcel.2011.10.030. PMC  3266520. PMID  22264730.
  8. ^ Carmeliet, P; Jain, RK (2011). "Molecular mechanisms and clinical applications of angiogenesis". Nature. 473 (7347): 298–307. Bibcode: 2011Natur.473..298C. doi: 10.1038/nature10144. PMC  4049445. PMID  21593862.

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