Roundabout (gene family)

roundabout
Identifiers
Organism Drosophila melanogaster
Symbol robo
Alt. symbols robo1
Entrez 37603
RefSeq (mRNA) NM_057551.3
RefSeq (Prot) NP_476899.1
UniProt Q7KVK3
Other data
Chromosome 2R: 18.58 - 18.59 Mb
leak
Identifiers
Organism Drosophila melanogaster
Symbol lea
Alt. symbols robo2
Entrez 44522
RefSeq (mRNA) NM_080531.3
RefSeq (Prot) NP_536792.2
UniProt Q9VQ08
Other data
Chromosome 2L: 1.37 - 1.43 Mb
robo3
Identifiers
Organism Drosophila melanogaster
Symbol robo3
Alt. symbols robo3
Entrez 33314
RefSeq (mRNA) NM_134748.2
RefSeq (Prot) NP_608592.2
UniProt Q9VPZ7
Other data
Chromosome 2L: 1.25 - 1.3 Mb
roundabout homolog 1
Identifiers
Symbol ROBO1
Entrez 6091
HUGO 10249
OMIM 602430
RefSeq NM_002941
UniProt Q9Y6N7
Other data
Locus Chr. 3 p12.3
roundabout homolog 2
Identifiers
Symbol ROBO2
Entrez 6092
HUGO 10250
OMIM 602431
RefSeq XM_031246
UniProt Q9HCK4
Other data
Locus Chr. 3 p12.3
roundabout homolog 3
Identifiers
Symbol ROBO3
Entrez 64221
HUGO 13433
OMIM Q96MS0
RefSeq XM_370663
UniProt Q96MS0
Other data
Locus Chr. 11 q24
roundabout homolog 4
Identifiers
Symbol ROBO4
Entrez 54538
HUGO 17985
OMIM 607528
RefSeq NM_019055
UniProt Q8WZ75
Other data
Locus Chr. 11 q24.2

The Roundabout (Robo) family of proteins are single-pass transmembrane receptors that are highly conserved across many branches of the animal kingdom, from C. elegans to humans.[1] They were first discovered in Drosophila, through a mutant screen for genes involved in axon guidance. The Drosophila roundabout mutant was named after its phenotype, which resembled the circular traffic junctions (see roundabout).[2] The Robo receptors are most well known for their role in the development of the nervous system, where they have been shown to respond to secreted Slit ligands.[2][3][4] One well-studied example is the requirement for Slit-Robo signaling in regulation of axonal midline crossing. Slit-Robo signaling is also critical for many neurodevelopmental processes including formation of the olfactory tract, the optic nerve, and motor axon fasciculation.[5][6] In addition, Slit-Robo signaling contributes to cell migration and the development of other tissues such as the lung, kidney, liver, muscle and breast.[7][8] Mutations in Robo genes have been linked to multiple neurodevelopmental disorders in humans.

Discovery

A large-scale screen of the Drosophila genome for mutants that exhibited axon guidance defects led to the discovery of the roundabout (robo) mutation.[9] In robo mutants, axons were observed to inappropriately cross and recross the midline. It was subsequently found that the secreted protein Slit was the ligand for the Roundabout receptor.[10] Vertebrate Slit proteins were identified shortly after, and were shown to bind both vertebrate and Drosophila Robo receptors and to mediate axonal repulsion of spinal cord explants.[4] It was several more years before a functional analysis of the vertebrate Slit and Robo mutants was performed; this analysis demonstrated that Slit-Robo signaling regulates commissural axon guidance in vertebrates as well.[11] Interestingly, while the vertebrate receptors Robo1 and Robo2 signal repulsion in response to Slit to prevent inappropriate midline crossing, a novel function for Robo3/Rig1 was discovered; unlike the other Robo receptors, it is required to promote midline crossing. [12]

Evolution of the family members

Phylogenetic analysis reveals that all Robo receptors have evolved from a common ancestral protein, with many subsequent diversification events occurring independently in different lineages.[1] The Robo gene was initially identified in Drosophila and has since been cloned in various species including mice and humans.[13] Drosophila have three Robo receptors: Robo1, Robo2, and Robo3.[14][15] In vertebrates, four Robo receptors have been identified: Robo1, Robo2, Robo3/Rig-1, and Robo4/Magic Roundabout.[16]

Genes

Location

In humans, Robo1 and Robo2 are located on chromosome 3p12.3, while Robo3 and Robo4 are found on chromosome 11p24.2. In mice, the corresponding Robo genes 1 and 2 are found on chromosome 16 and Robo genes 3 and 4 are located on chromosome 9.

Alternative splicing

In vertebrates, Robo1 undergoes complex alternative splicing, generating several isoforms including DUTT1, a variant that has been identified as a tumor suppressor gene.[17] Vertebrate Robo3/Rig1 is also alternatively spliced; its two splice products are expressed at different times during commisural axon guidance, and have opposing activities.[18]

Tissue distribution

In humans, Robo1 is expressed generally throughout the central nervous system.[17] Robo2 is enriched in most regions of the adult and fetal brain, as well as in the adult ovary. Intermediate expression of Robo2 is seen in the fetal liver and adult lung, kidney, spleen, testes, and spinal cord.[19] Robo3/Rig1 is found in the hindbrain and spinal cord.[20] Robo4 is expressed in the heart, liver, lungs, kidney, muscle, small intestine, endothelial cells, and largely in the placenta.[21]

Protein structure

Each member of the Robo family has a similar structure, consisting of five immunoglobulin-like domains, three fibronectin type III (FN3) repeats, a transmembrane domain, and a cytoplasmic domain with up to four conserved motifs (CC0-3). In all identified Robo receptors except for vertebrate Robo4, the Ig1 and Ig2 domains have been evolutionarily conserved and are crucial for binding to Slit ligands. Robo4 is unusual as it only contains two Ig and FN3 domains. However, recent research proposes that the vertebrate Slit2 protein can in fact bind to Robo4.[22]

Function

Robo-Slit Interactions and Axonal Midline Guidance

Axonal guidance

In bilaterian animals, including insects and mammals, most axons in the CNS cross the midline during nervous system development. The Robo proteins are critical regulators of midline crossing across species. In Drosophila embryos, Robo1 and Robo2 are required to keep ipsilaterally projecting axons from inappropriately crossing the midline, and to prevent contralateral axons from remaining stuck at the midline. Robo3, while it also binds Slit, does not appear to play a major role in regulating midline crossing. Instead, it is required for the lateral pathway selection of axons after crossing.[14] Robo2 also contributes to lateral pathway formation.

In the vertebrate spinal cord, Robo1 and Robo2 are expressed on commissural axons and act as repulsive receptors for the Slit ligands expressed by floor plate cells located at the midline.[11] In contrast, Robo3/Rig1 is required for midline crossing, and acts in part by antagonizing Slit-mediated repulsion by Robo1 and Robo2.[23]

Robo receptors have also been shown to be crucial regulators of many other axon pathfinding decisions during development, including the projection of axons in the optic tract and in the olfactory epithelium.[5][6]

Mutant Robo Receptors and Axonal Midline Crossing

Guidance of non-neural cells

The Robo gene family contributes to the guidance and migration of non-neural cells, including neuronal precursor cells, muscle cells, tracheal cells, Langerhans cells, and vascular smooth muscle cells.

Glioma invasion and migration inhibition

Robo1 is thought to play a role in the inhibition of glioma invasion and migration. Glioblastoma cells grow away from areas that contain high concentrations of Slit2 and its receptor Robo1, suggesting that the Robo1/Slit2 complex can serve as a chemorepellent for glioma cells, inhibiting the invasion and migration of the tumor cells.

Actin cytoskeleton regulation

The binding of Slit to Robo receptors leads to reorganization of the actin cytoskeleton. Actin polymerization is regulated by several adaptor proteins that can bind to the cytoplasmic motifs of the Robo receptors. In Drosophila, several signaling proteins downstream of Robo1 have been identified, including Enabled, Son of Sevenless (SOS), Rac, and Dock.[24][25][26] It is thought that activation of Robo1 by Slit leads to increased depolymerization of actin, resulting in growth cone collapse. It remains unclear how Drosophila Robo2 and Robo3 signal, although multiple studies suggest that they have distinct signaling capabilities that cannot be recapitulated by Robo1.[27][28]

Midline attraction and Robo3

The vertebrate Robo3/Rig1 homolog is a more distant relative of the Robo gene family, and is thought to play a distinct role in axonal guidance.[16][29] Robo3/Rig1 is alternatively spliced to generate a protein that inhibits Robo1/2-mediated repulsion, effectively leading to the promotion of midline crossing.[23] The exact mechanism by which Robo3 achieves this anti-repulsive activity is unknown.[29]

Clinical applications and areas of research

Angiogenesis and tumor suppression

The Robo4 receptor has been linked to angiogenesis in both mice and zebrafish. It is also present in human microvascular endothelial cells (HMVEC) and human umbilical vein endothelial cells (HUVEC). Exposure of Robo4 to Slit2 inhibits angiogenesis. However, exposure to a protein that inhibits Slit2 also inhibits angiogenesis.[30] Due to these inconclusive results, the role of Robo4 in blood vessel growth is not completely understood.

Robo1 has been linked to cancerous tumor growth and suppression. The Slit2/Robo1 pathway has been associated with tumor angiogenesis, leading to subsequent tumor growth. Slit2 proteins have been identified in several varieties of tumors, including melanoma, breast cancer, small cell lung cancer, and bladder cancer. Furthermore, inhibition of the Slit2/Robo1 pathway via R5 and RoboN reduced tumor mass and volume, while also reducing microvessel density.[31] However, Slit2 proteins have not been identified in all kinds of tumors, and other research suggests that Slit-2 expression may suppress tumors in small cell lung cancer and breast cancer.[30]

Dyslexia

The Robo1 protein is thought to be associated with dyslexia, possibly through chromosomal translocation.[32] The role of Robo1 in regards to dyslexia is not fully understood at this time.

Psychopathy

Recently, a genome-wide linkage study by Viding and colleagues (2010)reported that the Robo2 gene could be involved in developmental disorders such as psychopathy.

Robo3/Rig1 and HGPPS

A defect in the Robo3/Rig1 protein results in horizontal gaze palsy with progressive scoliosis (HGPPS), a rare genetic disorder. HGPPS is characterized by a lack of horizontal eye movement within the socket (although vertical movement remains unaffected) and the gradual curvature of the spine throughout development.[33][34] The disorder is caused by a genetic mutation on chromosome 11, and is autosomal recessive.[35] During normal brain development, Robo3/Rig1 decreases sensitivity of Robo1 to Slit proteins, allowing the axon to grow past the midline.[34] This process allows axons to cross to the other side of the brain, which is crucial for motor function as well as sensory processing. In patients with HGPPS, the absence of Robo3/Rig1 prevents axons in the corticospinal tract and the trochlear nerve[33] from growing past the midline. This abnormal growth of the hindbrain and spinal cord manifests itself as the symptoms associated with HGPPS.

References

  1. 1 2 Evans TA, Bashaw GJ (March 2012). "Slit/Robo-mediated axon guidance in Tribolium and Drosophila: divergent genetic programs build insect nervous systems". Dev. Biol. 363 (1): 266–78. doi:10.1016/j.ydbio.2011.12.046. PMID 22245052.
  2. 1 2 Kidd T, Brose K, Mitchell KJ, Fetter RD, Tessier-Lavigne M, Goodman CS, Tear G (January 1998). "Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors". Cell 92 (2): 205–15. doi:10.1016/S0092-8674(00)80915-0. PMID 9458045.
  3. ↑ Battye R, Stevens A, Jacobs JR (June 1999). "Axon repulsion from the midline of the Drosophila CNS requires slit function". Development 126 (11): 2475–81. PMID 10226006.
  4. 1 2 Brose K, Bland KS, Wang KH, Arnott D, Henzel W, Goodman CS, Tessier-Lavigne M, Kidd T (March 1999). "Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance". Cell 96 (6): 795–806. doi:10.1016/S0092-8674(00)80590-5. PMID 10102268.
  5. 1 2 Li HS, Chen JH, Wu W, Fagaly T, Zhou L, Yuan W, Dupuis S, Jiang ZH, Nash W, Gick C, Ornitz DM, Wu JY, Rao Y (March 1999). "Vertebrate slit, a secreted ligand for the transmembrane protein roundabout, is a repellent for olfactory bulb axons". Cell 96 (6): 807–18. doi:10.1016/S0092-8674(00)80591-7. PMID 10102269.
  6. 1 2 Fricke C, Lee JS, Geiger-Rudolph S, Bonhoeffer F, Chien CB (April 2001). "astray, a zebrafish roundabout homolog required for retinal axon guidance". Science 292 (5516): 507–10. doi:10.1126/science.1059496. PMID 11313496.
  7. ↑ Englund C, Steneberg P, Falileeva L, Xylourgidis N, Samakovlis C (November 2002). "Attractive and repulsive functions of Slit are mediated by different receptors in the Drosophila trachea". Development 129 (21): 4941–51. PMID 12397103.
  8. ↑ Kramer SG, Kidd T, Simpson JH, Goodman CS (April 2001). "Switching repulsion to attraction: changing responses to slit during transition in mesoderm migration". Science 292 (5517): 737–40. doi:10.1126/science.1058766. PMID 11326102.
  9. ↑ Seeger M, Tear G, Ferres-Marco D, Goodman CS (March 1993). "Mutations affecting growth cone guidance in Drosophila: genes necessary for guidance toward or away from the midline". Neuron 10 (3): 409–26. doi:10.1016/0896-6273(93)90330-T. PMID 8461134.
  10. ↑ Kidd T, Bland KS, Goodman CS (March 1999). "Slit is the midline repellent for the robo receptor in Drosophila". Cell 96 (6): 785–94. doi:10.1016/S0092-8674(00)80589-9. PMID 10102267.
  11. 1 2 Long H, Sabatier C, Ma L, Plump A, Yuan W, Ornitz DM, Tamada A, Murakami F, Goodman CS, Tessier-Lavigne M (April 2004). "Conserved roles for Slit and Robo proteins in midline commisural axon guidance". Neuron 42 (2): 213–23. doi:10.1016/S0896-6273(04)00179-5. PMID 15091338.
  12. ↑ Sabatier C, Plump A, Ma L, Brose K, Tamada A, Murakami F, Lee E, Tessier-Lavigne M (April 2004). "The divergent Robo family protein rig-1/Robo3 is a negative regulator of Slit responsiveness required for midline crossing by commisural axons". Cell 117 (2): 157–69. doi:10.1016/S0092-8674(04)00303-4. PMID 15084255.
  13. ↑ Fujiwara M, Ghazizadeh M, Kawanami O (May 2006). "Potential role of the Slit/Robo signal pathway in angiogenesis". Vasc Med 11 (2): 115–21. doi:10.1191/1358863x06vm658ra. PMID 16886842.
  14. 1 2 Simpson JH, Bland KS, Fetter RD, Goodman CS (December 2000). "Short-range and long-range guidance by Slit and its Robo receptors: a combinatorial code of Robo receptors controls lateral position". Cell 103 (7): 1019–32. doi:10.1016/S0092-8674(00)00206-3. PMID 11163179.
  15. ↑ Rajagopalan S, Vivancos V, Nicolas E, Dickson BJ (December 2000). "Selecting a longitudinal pathway: Robo receptors specify the lateral position of axons in the Drosophila CNS". Cell 103 (7): 1033–45. doi:10.1016/S0092-8674(00)00207-5. PMID 11163180.
  16. 1 2 Xu Y, Li WL, Fu L, Gu F, Ma YJ (December 2010). "Slit2/Robo1 signaling in glioma migration and invasion". Neurosci Bull 26 (6): 474–8. doi:10.1007/s12264-010-0730-9. PMID 21113198.
  17. 1 2 Online 'Mendelian Inheritance in Man' (OMIM) 602430
  18. ↑ Chen S, Gore BB, Long H, Ma L, Tessier-Lavigne M (May 2008). "Alternative splicing of the Robo3 axon guidance receptor governs the midline switch from attraction to repulsion". Neuron 58 (3): 325–32. doi:10.1016/j.neuron.2008.02.016. PMID 18466743.
  19. ↑ Online 'Mendelian Inheritance in Man' (OMIM) 602431
  20. ↑ Online 'Mendelian Inheritance in Man' (OMIM) 608630
  21. ↑ Online 'Mendelian Inheritance in Man' (OMIM) 607528
  22. ↑ Dickinson, R. E; Duncan, W C. (25 January 2010). "The SLIT-ROBO pathway: a regulator of cell function with implications for the reproductive system". Reproduction 139 (4): 697–704. doi:10.1530/REP-10-0017. PMC 2971463. PMID 20100881.
  23. 1 2 Marillat V, Sabatier C, Failli V, Matsunaga E, Sotelo C, Tessier-Lavigne M, Chédotal A (July 2004). "The slit receptor Rig-1/Robo3 controls midline crossing by hindbrain precerebellar neurons and axons". Neuron 43 (1): 69–79. doi:10.1016/j.neuron.2004.06.018. PMID 15233918.
  24. ↑ Bashaw GJ, Kidd T, Murray D, Pawson T, Goodman CS (June 2000). "Repulsive axon guidance: Abelson and Enabled play opposing roles downstream of the roundabout receptor". Cell 101 (7): 703–15. doi:10.1016/S0092-8674(00)80883-1. PMID 10892742.
  25. ↑ Fan X, Labrador JP, Hing H, Bashaw GJ (September 2003). "Slit stimulation recruits Dock and Pak to the roundabout receptor and increases Rac activity to regulate axon repulsion at the CNS midline". Neuron 40 (1): 113–27. doi:10.1016/S0896-6273(03)00591-9. PMID 14527437.
  26. ↑ Hu H, Li M, Labrador JP, McEwen J, Lai EC, Goodman CS, Bashaw GJ (March 2005). "Cross GTPase-activating protein (CrossGAP)/Vilse links the Roundabout receptor to Rac to regulate midline repulsion". Proc. Natl. Acad. Sci. U.S.A. 102 (12): 4613–8. doi:10.1073/pnas.0409325102. PMC 555501. PMID 15755809.
  27. ↑ Spitzweck B, Brankatschk M, Dickson BJ (February 2010). "Distinct protein domains and expression patterns confer divergent axon guidance functions for Drosophila Robo receptors". Cell 140 (3): 409–20. doi:10.1016/j.cell.2010.01.002. PMID 20144763.
  28. ↑ Evans TA, Bashaw GJ (March 2010). "Functional diversity of Robo receptor immunoglobulin domains promotes distinct axon guidance decisions". Curr. Biol. 20 (6): 567–72. doi:10.1016/j.cub.2010.02.021. PMID 20206526.
  29. 1 2 Guthrie S (August 2004). "Axon guidance: mice and men need Rig and Robo". Curr. Biol. 14 (15): R632–4. doi:10.1016/j.cub.2004.07.050. PMID 15296783.
  30. 1 2 Klagsbrun M, Eichmann A (2005). "A role for axon guidance receptors and ligands in blood vessel development and tumor angiogenesis". Cytokine Growth Factor Rev. 16 (4–5): 535–48. doi:10.1016/j.cytogfr.2005.05.002. PMID 15979925.
  31. ↑ Wang B, Xiao Y, Ding BB, Zhang N, Yuan X, Gui L, Qian KX, Duan S, Chen Z, Rao Y, Geng JG (July 2003). "Induction of tumor angiogenesis by Slit-Robo signaling and inhibition of cancer growth by blocking Robo activity". Cancer Cell 4 (1): 19–29. doi:10.1016/S1535-6108(03)00164-8. PMID 12892710.
  32. ↑ Galaburda AM, LoTurco J, Ramus F, Fitch RH, Rosen GD (October 2006). "From genes to behavior in developmental dyslexia". Nat. Neurosci. 9 (10): 1213–7. doi:10.1038/nn1772. PMID 17001339.
  33. 1 2 Purves D (2011). Neuroscience. Sunderland, Mass: Sinauer Associates, Inc. ISBN 0-87893-695-5.
  34. 1 2 Butcher J (June 2004). "Mutations in ROBO3 cause HGPPS". Lancet Neurol 3 (6): 328. doi:10.1016/S1474-4422(04)00786-0. PMID 15176408.
  35. ↑ "Horizontal gaze palsy with progressive scoliosis". Retrieved 2012-04-17.
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