Blood vessel epicardial substance explained

Blood vessel epicardial substance (BVES) also known as popeye domain-containing protein 1 (POPDC1) is a protein that is encoded by the BVES gene in humans.[1]

Bves is a highly conserved, transmembrane protein that is involved in cell adhesion, cell motility, and most recently has been shown to play a role in vesicular transport.[2] [3] [4] [5] Bves is found in a wide variety of organisms (from flies to humans) and is a member of the evolutionarily conserved Popdc family of proteins. Although the precise molecular function of Bves is unknown, disruption of this protein results in developmental defects and impaired cellular processes fundamental to living organisms.[6] [7] [8]

Discovery

Bves was discovered simultaneously by two independent labs in 1999 (Bves was also named Popdc1 at the time of discovery; the current accepted convention is Bves).[9] [10] Although initially isolated from cardiac tissue, it was later revealed that Bves is highly expressed in muscle, epithelial and brain tissue.[3] Most studies have focused on determining the function of Bves in epithelial tissue at the cellular level.

Gene family

Bves is the most studied member of the Popeye domain containing (Popdc) family of genes. The two other members of this family are Popdc2 and Popdc3. Popdc2 and Popdc3 are only found in higher vertebrates and share 50% of their DNA sequence, whereas Bves is only 25% homologous with the evolutionary younger Popdc family members. All three members of the Popdc family contain the highly conserved Popeye domain as the family was named for this specific protein motif.[2] [3] [4]

Structure

Bves is a three-pass transmembrane protein with a short extracellular N-terminus (~40aa) and a larger intracellular C-terminus (~250aa).[11] Within the C-terminus is the Popeye domain, which has been postulated to be important for Bves function. The Popeye domain shares no homology with any known protein motifs, and specific function of this domain is currently unknown, although it is highly conserved across species. Bves exists as a homodimer in vivo, and homodimerization has been shown to be important for function.[12]

Localization/expression

Bves is expressed in muscle, epithelial and brain tissue, and is thus found in many adult organs.[4] During development, Bves is detected in all three germ layers and later localizes to the aforementioned tissues.[13] Subcellular localization is present at the plasma membrane and is also seen in punctate, intracellular vesicles. Bves demonstrates dynamic localization, dependent upon cell-cell junction formation. Prior to cell-cell contact, Bves is localized mostly to intracellular vesicles, but as cells begin to form associations, Bves is also present at points of cell-cell contact.[6]

Interacting proteins

Bves interacts with GEFT, a protein that modulates Rho GTPases, Rac1 and Cdc42, which are important for cell motility through modulation of the actin cytoskeleton.[8] Bves also interacts with VAMP3, a SNARE protein important for vesicle fusion.[5] Additionally, Bves has been shown to interact with the tight junction protein, ZO1, although this interaction is most likely via a protein complex, as a direct physical interaction has never been demonstrated.[6]

Function

Disruption of Bves results in a wide range of cellular and developmental phenotypes. Grossly, cell motility and cell adhesion are impaired. Only recently have the molecular mechanisms underlying the function of Bves been uncovered.

Modulation of Rho GTPases

Bves has been shown to interact and co-localize with GEFT, a modulator of Rho GTPase signaling cascades. Disruption of Bves results in decreased cell speed and increased cell roundness, which are cell processes modulated by the Rho GTPases, Rac1 and Cdc42. Accordingly, Bves disruption results in decreased active Rac1 and Cdc42. Taken together, these data demonstrate that Bves modulates Rho GTPase signaling cascades through interaction with GEFT to affect cell movement and morphology.[8]

Regulation of vesicular transport

Bves has been shown to interact with VAMP3, a member of the SNARE complex that facilitates vesicle fusion. VAMP3 is important for recycling of integrins during cell migration and is also necessary for exocytosis of transferrin.[14] [15] [16] [17] [18] Upon Bves disruption, cell rounding is increased, a phenotype indicative of decreased adhesion and disruption of integrin function. Accordingly, Bves disruption results in impaired integrin recycling, phenocopying the result seen with inhibition of VAMP3. Similarly, disruption of either Bves results in impaired transferrin recycling again, mimicking the result seen with disruption of VAMP3. Thus, Bves is important for VAMP3-mediated vesicular transport underlying cell migration and transferrin recycling.[5]

Silencing in malignancy

Bves is silenced by promoter hypermethylation in malignancy. Bves is underexpressed in colon, lung, and breast cancer. In colon cancer this occurs very early during tumorigenesis, with Bves underexpression first noted in premalignant adenomas.

Notes and References

  1. Reese DE, Bader DM . Cloning and expression of hbves, a novel and highly conserved mRNA expressed in the developing and adult heart and skeletal muscle in the human . Mammalian Genome . 10 . 9 . 913–5 . Sep 1999 . 10441744 . 10.1007/s003359901113 . 35384190 .
  2. Brand T . The Popeye domain-containing gene family . . 43 . 1 . 95–103 . 2005 . 16043887 . 10.1385/CBB:43:1:095 . 13142874 .
  3. Osler ME, Smith TK, Bader DM . Bves, a member of the Popeye domain-containing gene family . Developmental Dynamics . 235 . 3 . 586–93 . Mar 2006 . 16444674 . 2849751 . 10.1002/dvdy.20688 .
  4. Hager HA, Bader DM . Bves: ten years after . Histology and Histopathology . 24 . 6 . 777–87 . Jun 2009 . 19337975 . 2853719 .
  5. Hager HA, Roberts RJ, Cross EE, Proux-Gillardeaux V, Bader DM . Identification of a novel Bves function: regulation of vesicular transport . The EMBO Journal . 29 . 3 . 532–45 . Feb 2010 . 20057356 . 2830705 . 10.1038/emboj.2009.379 .
  6. Osler ME, Chang MS, Bader DM . Bves modulates epithelial integrity through an interaction at the tight junction . Journal of Cell Science . 118 . Pt 20 . 4667–78 . Oct 2005 . 16188940 . 10.1242/jcs.02588 . free .
  7. Ripley AN, Osler ME, Wright CV, Bader D . Xbves is a regulator of epithelial movement during early Xenopus laevis development . Proceedings of the National Academy of Sciences of the United States of America . 103 . 3 . 614–9 . Jan 2006 . 16407138 . 1334639 . 10.1073/pnas.0506095103 . 2006PNAS..103..614R . free .
  8. Smith TK, Hager HA, Francis R, Kilkenny DM, Lo CW, Bader DM . Bves directly interacts with GEFT, and controls cell shape and movement through regulation of Rac1/Cdc42 activity . Proceedings of the National Academy of Sciences of the United States of America . 105 . 24 . 8298–303 . Jun 2008 . 18541910 . 2423412 . 10.1073/pnas.0802345105 . 2008PNAS..105.8298S . free .
  9. Andrée B, Hillemann T, Kessler-Icekson G, Schmitt-John T, Jockusch H, Arnold HH, Brand T . Isolation and characterization of the novel popeye gene family expressed in skeletal muscle and heart . Developmental Biology . 223 . 2 . 371–82 . Jul 2000 . 10882522 . 10.1006/dbio.2000.9751 . free .
  10. Reese DE, Zavaljevski M, Streiff NL, Bader D . bves: A novel gene expressed during coronary blood vessel development . Developmental Biology . 209 . 1 . 159–71 . May 1999 . 10208750 . 10.1006/dbio.1999.9246 . free .
  11. Knight RF, Bader DM, Backstrom JR . Membrane topology of Bves/Pop1A, a cell adhesion molecule that displays dynamic changes in cellular distribution during development . The Journal of Biological Chemistry . 278 . 35 . 32872–9 . Aug 2003 . 12815060 . 10.1074/jbc.M301961200 . free .
  12. Kawaguchi M, Hager HA, Wada A, Koyama T, Chang MS, Bader DM . Identification of a novel intracellular interaction domain essential for Bves function . PLOS ONE . 3 . 5 . e2261 . 2008 . 18493308 . 2373926 . 10.1371/journal.pone.0002261 . 2008PLoSO...3.2261K . free .
  13. Osler ME, Bader DM . Bves expression during avian embryogenesis . Developmental Dynamics . 229 . 3 . 658–67 . Mar 2004 . 14991721 . 10.1002/dvdy.10490 . 12458928 . free .
  14. McMahon HT, Ushkaryov YA, Edelmann L, Link E, Binz T, Niemann H, Jahn R, Südhof TC . Cellubrevin is a ubiquitous tetanus-toxin substrate homologous to a putative synaptic vesicle fusion protein . Nature . 364 . 6435 . 346–9 . Jul 1993 . 8332193 . 10.1038/364346a0 . 1993Natur.364..346M . 4324845 .
  15. Proux-Gillardeaux V, Gavard J, Irinopoulou T, Mège RM, Galli T . Tetanus neurotoxin-mediated cleavage of cellubrevin impairs epithelial cell migration and integrin-dependent cell adhesion . Proceedings of the National Academy of Sciences of the United States of America . 102 . 18 . 6362–7 . May 2005 . 15851685 . 1088364 . 10.1073/pnas.0409613102 . 2005PNAS..102.6362P . free .
  16. Skalski M, Coppolino MG . SNARE-mediated trafficking of alpha5beta1 integrin is required for spreading in CHO cells . Biochemical and Biophysical Research Communications . 335 . 4 . 1199–210 . Oct 2005 . 16112083 . 10.1016/j.bbrc.2005.07.195 .
  17. Tayeb MA, Skalski M, Cha MC, Kean MJ, Scaife M, Coppolino MG . Inhibition of SNARE-mediated membrane traffic impairs cell migration . Experimental Cell Research . 305 . 1 . 63–73 . Apr 2005 . 15777788 . 10.1016/j.yexcr.2004.12.004 .
  18. Luftman K, Hasan N, Day P, Hardee D, Hu C . Silencing of VAMP3 inhibits cell migration and integrin-mediated adhesion . Biochemical and Biophysical Research Communications . 380 . 1 . 65–70 . Feb 2009 . 19159614 . 2716655 . 10.1016/j.bbrc.2009.01.036 .