Skip to main content
Log in

Rho-linked genes and neurological disorders

  • Invited Review
  • Published:
Pflügers Archiv - European Journal of Physiology Aims and scope Submit manuscript

Abstract

Mental retardation (MR) is a common cause of intellectual disability and affects approximately 2 to 3% of children and young adults. Many forms of MR are associated with abnormalities in dendritic structure and/or dendritic spine morphology. Given that dendritic spine morphology has been tightly linked to synaptic activity, altered spine morphology has been suggested to underlie or contribute to the cognitive disabilities associated with MR. The structure and dynamics of dendritic spines is determined by its underlying actin cytoskeleton. Signaling molecules and cascades important for cytoskeletal regulation have therefore attracted a great deal of attention. As key regulators of both the actin and microtubule cytoskeletons, it is not surprising that the Rho GTPases have emerged as important regulators of dendrite and spine structural plasticity. Significantly, mutations in regulators and effectors of Rho GTPases have been associated with diseases affecting the nervous system, including MR and amyotropic lateral sclerosis (ALS). Here, we will discuss Rho GTPase-related genes and their signaling pathways involved in MR and ALS.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Abbreviations

AD:

Alzheimer disease

ALS:

amyotropic lateral sclerosis

AMPAR:

α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor

ARHGEF6:

Rho guanine–nucleotide exchange factor 6

Arp2/3:

actin-related proteins 2 and 3

Aβ:

amyloid β

CREB:

cAMP-responsive element-binding protein

CYFIP:

cytoplasmic FMR1 interacting protein

FMRP:

fragile-X mental retardation protein

FMR1:

fragile-X mental retardation-1 gene

FRAXA:

fragile-X syndrome

GAP:

GTPase activating proteins

GDI:

guanine–nucleotide dissociation inhibitor

GEF:

guanine–nucleotide exchange factor

LIM:

Lin-11, Isl-1, and Mec-3 kinase

LTD:

long-term depression

LTP:

long-term potentiation

MEGAP:

mental disorder-associated GAP protein

mGluR:

metabotropic glutamate receptor

MLC:

myosin light chain

MLCK:

myosin light chain kinase

MLCP:

myosin light chain phosphatase

MR:

mental retardation

MRX:

non-syndromic X-linked mental retardation

MRXS:

syndromic X-linked mental retardation

OPHN1:

oligophrenin-1

PAK:

p21-activated kinases

ROCK:

Rho-Kinase

WASP:

Wiskott–Aldrich syndrome protein

WAVE:

WASP family Verprolin-homologous protein

WS:

Williams–Beuren syndrome

XLMR:

X-linked mental retardation

References

  1. Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA (1998) PAK3 mutation in nonsyndromic X-linked mental retardation. Nat Genet 20:25–30

    Article  PubMed  CAS  Google Scholar 

  2. Ang LH, Chen W, Yao Y, Ozawa R, Tao E, Yonekura J, Uemura T, Keshishian H, Hing H (2006) Lim kinase regulates the development of olfactory and neuromuscular synapses. Dev Biol 293:178–190

    Article  PubMed  CAS  Google Scholar 

  3. Arber S, Barbayannis FA, Hanser H, Schneider C, Stanyon CA, Bernard O, Caroni P (1998) Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase. Nature 393:805–809

    Article  PubMed  CAS  Google Scholar 

  4. Bear MF, Huber KM, Warren ST (2004) The mGluR theory of fragile X mental retardation. Trends Neurosci 27:370–377

    Article  PubMed  CAS  Google Scholar 

  5. Bergmann C, Zerres K, Senderek J, Rudnik-Schoneborn S, Eggermann T, Hausler M, Mull M, Ramaekers VT (2003) Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia. Brain 126:1537–1544

    Article  PubMed  Google Scholar 

  6. Bienvenu T, Der-Sarkissian H, Billuart P, Tissot M, Des Portes V, Bruls T, Chabrolle JP, Chauveau P, Cherry M, Kahn A, Cohen D, Beldjord C, Chelly J, Cherif D (1997) Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation. Eur J Hum Genet 5:105–109

    PubMed  CAS  Google Scholar 

  7. Bienvenu T, des Portes V, McDonell N, Carrie A, Zemni R, Couvert P, Ropers Chelly J, Beldjord C (2000) Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. Am J Med Genet 93:294–298

    Article  PubMed  CAS  Google Scholar 

  8. Billuart P, Bienvenu T, Ronce N, des Portes V, Vinet MC, Zemni R, Roest Crollius H, Carrie A, Fauchereau F, Cherry M, Briault S, Hamel B, Fryns JP, Beldjord C, Kahn A, Moraine C, Chelly J (1998) Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. Nature 392:923–926

    Article  PubMed  CAS  Google Scholar 

  9. Boda B, Alberi S, Nikonenko I, Node-Langlois R, Jourdain P, Moosmayer M, Parisi-Jourdain L, Muller D (2004) The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus. J Neurosci 24:10816–10825

    Article  PubMed  CAS  Google Scholar 

  10. Bokoch GM (2003) Biology of the p21-activated kinases. Annu Rev Biochem 72:743–781

    Article  PubMed  CAS  Google Scholar 

  11. Bruijn LI, Miller TM, Cleveland DW (2004) Unraveling the mechanisms involved in motor neuron degeneration in ALS. Annu Rev Neurosci 27:723–749

    Article  PubMed  CAS  Google Scholar 

  12. Cai H, Lin X, Xie C, Laird FM, Lai C, Wen H, Chiang HC, Shim H, Farah MH, Hoke A, Price DL, Wong PC (2005) Loss of ALS2 function is insufficient to trigger motor neuron degeneration in knock-out mice but predisposes neurons to oxidative stress. J Neurosci 25:7567–7574

    Article  PubMed  CAS  Google Scholar 

  13. Carlisle HJ, Kennedy MB (2005) Spine architecture and synaptic plasticity. Trends Neurosci 28:182–187

    Article  PubMed  CAS  Google Scholar 

  14. Castets M, Schaeffer C, Bechara E, Schenck A, Khandjian EW, Luche S, Moine H, Rabilloud T, Mandel JL, Bardoni B (2005) FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts. Hum Mol Genet 14:835–844

    Article  PubMed  CAS  Google Scholar 

  15. Chelly J, Mandel JL (2001) Monogenic causes of X-linked mental retardation. Nat Rev Genet 2:669–680

    Article  PubMed  CAS  Google Scholar 

  16. Cleveland DW, Rothstein JD (2001) From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS. Nat Rev Neurosci 2:806–819

    Article  PubMed  CAS  Google Scholar 

  17. Comery TA, Harris JB, Willems PJ, Oostra BA, Irwin SA, Weiler IJ, Greenough WT (1997) Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits. Proc Natl Acad Sci USA 94:5401–5404

    Article  PubMed  CAS  Google Scholar 

  18. Daniels RH, Zenke FT, Bokoch GM (1999) alphaPix stimulates p21-activated kinase activity through exchange factor-dependent and -independent mechanisms. J Biol Chem 274:6047–6050

    Article  PubMed  CAS  Google Scholar 

  19. Devon RS, Orban PC, Gerrow K, Barbieri MA, Schwab C, Cao LP, Helm JR, Bissada N, Cruz-Aguado R, Davidson TL, Witmer J, Metzler M, Lam CK, Tetzlaff W, Simpson EM, McCaffery JM, El-Husseini AE, Leavitt BR, Hayden MR (2006) Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci USA 103:9595–9600

    Article  PubMed  CAS  Google Scholar 

  20. Eden S, Rohatgi R, Podtelejnikov AV, Mann M, Kirschner MW (2002) Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck. Nature 418:790–793

    Article  PubMed  CAS  Google Scholar 

  21. Endris V, Wogatzky B, Leimer U, Bartsch D, Zatyka M, Latif F, Maher ER, Tariverdian G, Kirsch S, Karch D, Rappold GA (2002) The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation. Proc Natl Acad Sci U S A 99:11754–11759

    Article  PubMed  CAS  Google Scholar 

  22. Etienne-Manneville S, Hall A (2002) Rho GTPases in cell biology. Nature 420:629–635

    Article  PubMed  CAS  Google Scholar 

  23. Fagni L, Worley PF, Ango F (2002) Homer as both a scaffold and transduction molecule. Sci STKE 2002:RE8

    Article  PubMed  Google Scholar 

  24. Fauchereau F, Herbrand U, Chafey P, Eberth A, Koulakoff A, Vinet MC, Ahmadian MR, Chelly J, Billuart P (2003) The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain. Mol Cell Neurosci 23:574–586

    Article  PubMed  CAS  Google Scholar 

  25. Fiala JC, Spacek J, Harris KM (2002) Dendritic spine pathology: cause or consequence of neurological disorders? Brain Res Brain Res Rev 39:29–54

    Article  PubMed  Google Scholar 

  26. Foa L, Jensen K, Rajan I, Bronson K, Gasperini R, Worley PF, Tu JC, Cline HT (2005) Homer expression in the Xenopus tadpole nervous system. J Comp Neurol 487:42–53

    Article  PubMed  CAS  Google Scholar 

  27. Garber K, Smith KT, Reines D, Warren ST (2006) Transcription, translation and fragile X syndrome. Curr Opin Genet Dev 16:270–275

    Article  PubMed  CAS  Google Scholar 

  28. Gecz J (2004) The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain. Front Biosci 9:1–7

    Article  PubMed  CAS  Google Scholar 

  29. Gedeon AK, Nelson J, Gecz J, Mulley JC (2003) X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3. Am J Med Genet A 120:509–517

    Article  PubMed  Google Scholar 

  30. Govek EE, Newey SE, Akerman CJ, Cross JR, Van der Veken L, Van Aelst L (2004) The X-linked mental retardation protein oligophrenin-1 is required for dendritic spine morphogenesis. Nat Neurosci 7:364–372

    Article  PubMed  CAS  Google Scholar 

  31. Govek EE, Newey SE, Van Aelst L (2005) The role of the Rho GTPases in neuronal development. Genes Dev 19:1–49

    Article  PubMed  CAS  Google Scholar 

  32. Grossman AW, Aldridge GM, Weiler IJ, Greenough WT (2006) Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond. J Neurosci 26:7151–7155

    Article  PubMed  CAS  Google Scholar 

  33. Gundersen GG, Gomes ER, Wen Y (2004) Cortical control of microtubule stability and polarization. Curr Opin Cell Biol 16:106–112

    Article  PubMed  CAS  Google Scholar 

  34. Hadano S, Benn SC, Kakuta S, Otomo A, Sudo K, Kunita R, Suzuki-Utsunomiya K, Mizumura H, Shefner JM, Cox GA, Iwakura Y, Brown RH Jr., Ikeda JE (2006) Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking. Hum Mol Genet 15:233–250

    Article  PubMed  CAS  Google Scholar 

  35. Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr., Scherer SW, Rouleau GA, Hayden MR, Ikeda JE (2001) A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat Genet 29:166–173

    Article  PubMed  CAS  Google Scholar 

  36. Hayashi ML, Choi SY, Rao BS, Jung HY, Lee HK, Zhang D, Chattarji S, Kirkwood A, Tonegawa S (2004) Altered cortical synaptic morphology and impaired memory consolidation in forebrain-specific dominant-negative PAK transgenic mice. Neuron 42:773–787

    Article  PubMed  CAS  Google Scholar 

  37. Heredia L, Helguera P, de Olmos S, Kedikian G, Sola Vigo F, LaFerla F, Staufenbiel M, de Olmos J, Busciglio J, Caceres A, Lorenzo A (2006) Phosphorylation of actin-depolymerizing factor/cofilin by LIM-kinase mediates amyloid beta-induced degeneration: a potential mechanism of neuronal dystrophy in Alzheimer’s disease. J Neurosci 26:6533–6542

    Article  PubMed  CAS  Google Scholar 

  38. Hering H, Sheng M (2001) Dendritic spines: structure, dynamics and regulation. Nat Rev Neurosci 2:880–888

    Article  PubMed  CAS  Google Scholar 

  39. Irwin SA, Patel B, Idupulapati M, Harris JB, Crisostomo RA, Larsen BP, Kooy F, Willems PJ, Cras P, Kozlowski PB, Swain RA, Weiler IJ, Greenough WT (2001) Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination. Am J Med Genet 98:161–167

    Article  PubMed  CAS  Google Scholar 

  40. Jacquier A, Buhler E, Schafer MK, Bohl D, Blanchard S, Beclin C, Haase G (2006) Alsin/Rac1 signaling controls survival and growth of spinal motoneurons. Ann Neurol 60:105–117

    Article  PubMed  CAS  Google Scholar 

  41. Jaffer ZM, Chernoff J (2002) p21-activated kinases: three more join the Pak. Int J Biochem Cell Biol 34:713–717

    Article  PubMed  CAS  Google Scholar 

  42. Kandel ER (2001) The molecular biology of memory storage: a dialogue between genes and synapses. Science 294:1030–1038

    Article  PubMed  CAS  Google Scholar 

  43. Kanekura K, Hashimoto Y, Kita Y, Sasabe J, Aiso S, Nishimoto I, Matsuoka M (2005) A Rac1/phosphatidylinositol 3-kinase/Akt3 anti-apoptotic pathway, triggered by AlsinLF, the product of the ALS2 gene, antagonizes Cu/Zn- superoxide dismutase (SOD1) mutant-induced motoneuronal cell death. J Biol Chem 280:4532–4543

    Article  PubMed  CAS  Google Scholar 

  44. Kasai H, Matsuzaki M, Noguchi J, Yasumatsu N, Nakahara H (2003) Structure–stability–function relationships of dendritic spines. Trends Neurosci 26:360–368

    Article  PubMed  CAS  Google Scholar 

  45. Kaufmann WE, Moser HW (2000) Dendritic anomalies in disorders associated with mental retardation. Cereb Cortex 10:981–991

    Article  PubMed  CAS  Google Scholar 

  46. Kennedy MB, Beale HC, Carlisle HJ, Washburn LR (2005) Integration of biochemical signalling in spines. Nat Rev Neurosci 6:423–434

    Article  PubMed  CAS  Google Scholar 

  47. Khelfaoui M, Denis C, van Galen E, de Bock F, Schmitt A, Houbron C, Morice E, Giros B, Ramakers G, Fagni L, Chelly J, Nosten-Bertrand M, Billuart P (2007) Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity. J Neurosci 27:9439–9450

    Article  PubMed  CAS  Google Scholar 

  48. Kim Y, Sung JY, Ceglia I, Lee KW, Ahn JH, Halford JM, Kim AM, Kwak SP, Park JB, Ho Ryu S, Schenck A, Bardoni B, Scott JD, Nairn AC, Greengard P (2006) Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology. Nature 442:814–817

    Article  PubMed  CAS  Google Scholar 

  49. Kobayashi K, Kuroda S, Fukata M, Nakamura T, Nagase T, Nomura N, Matsuura Y, Yoshida-Kubomura N, Iwamatsu A, Kaibuchi K (1998) p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase. J Biol Chem 273:291–295

    Article  PubMed  CAS  Google Scholar 

  50. Kopec CD, Li B, Wei W, Boehm J, Malinow R (2006) Glutamate receptor exocytosis and spine enlargement during chemically induced long-term potentiation. J Neurosci 26:2000–2009

    Article  PubMed  CAS  Google Scholar 

  51. Kutsche K, Yntema H, Brandt A, Jantke I, Nothwang HG, Orth U, Boavida MG, David D, Chelly J, Fryns JP, Moraine C, Ropers HH, Hamel BC, van Bokhoven H, Gal A (2000) Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation. Nat Genet 26:247–250

    Article  PubMed  CAS  Google Scholar 

  52. LaFerla FM, Oddo S (2005) Alzheimer’s disease: abeta, tau and synaptic dysfunction. Trends Mol Med 11:170–176

    Article  PubMed  CAS  Google Scholar 

  53. Lamprecht R, LeDoux J (2004) Structural plasticity and memory. Nat Rev Neurosci 5:45–54

    Article  PubMed  CAS  Google Scholar 

  54. Lee A, Li W, Xu K, Bogert BA, Su K, Gao FB (2003) Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1. Development 130:5543–5552

    Article  PubMed  CAS  Google Scholar 

  55. Lonze BE, Ginty DD (2002) Function and regulation of CREB family transcription factors in the nervous system. Neuron 35:605–623

    Article  PubMed  CAS  Google Scholar 

  56. Malinow R, Malenka RC (2002) AMPA receptor trafficking and synaptic plasticity. Annu Rev Neurosci 25:103–126

    Article  PubMed  CAS  Google Scholar 

  57. Mandel JL, Chelly J (2004) Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations. Eur J Hum Genet 12:689–693

    Article  PubMed  CAS  Google Scholar 

  58. Meng J, Meng Y, Hanna A, Janus C, Jia Z (2005) Abnormal long-lasting synaptic plasticity and cognition in mice lacking the mental retardation gene Pak3. J Neurosci 25:6641–6650

    Article  PubMed  CAS  Google Scholar 

  59. Meng Y, Zhang Y, Tregoubov V, Janus C, Cruz L, Jackson M, Lu WY, MacDonald JF, Wang JY, Falls DL, Jia Z (2002) Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice. Neuron 35:121–133

    Article  PubMed  CAS  Google Scholar 

  60. Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL (1993) Clinical and molecular analyses of deletion 3p25-pter syndrome. Am J Med Genet 46:623–629

    Article  PubMed  CAS  Google Scholar 

  61. Newey SE, Velamoor V, Govek EE, Van Aelst L (2005) Rho GTPases, dendritic structure, and mental retardation. J Neurobiol 64:58–74

    Article  PubMed  CAS  Google Scholar 

  62. Nimchinsky EA, Oberlander AM, Svoboda K (2001) Abnormal development of dendritic spines in FMR1 knock-out mice. J Neurosci 21:5139–5146

    PubMed  CAS  Google Scholar 

  63. Node-Langlois R, Muller D, Boda B (2006) Sequential implication of the mental retardation proteins ARHGEF6 and PAK3 in spine morphogenesis. J Cell Sci 119:4986–4993

    Article  PubMed  CAS  Google Scholar 

  64. Okamoto K, Nagai T, Miyawaki A, Hayashi Y (2004) Rapid and persistent modulation of actin dynamics regulates postsynaptic reorganization underlying bidirectional plasticity. Nat Neurosci 7:1104–1112

    Article  PubMed  CAS  Google Scholar 

  65. Otomo A, Hadano S, Okada T, Mizumura H, Kunita R, Nishijima H, Showguchi- Miyata J, Yanagisawa Y, Kohiki E, Suga E, Yasuda M, Osuga H, Nishimoto T, Narumiya S, Ikeda JE (2003) ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics. Hum Mol Genet 12:1671–1687

    Article  PubMed  CAS  Google Scholar 

  66. Pasinelli P, Brown RH (2006) Molecular biology of amyotrophic lateral sclerosis: insights from genetics. Nat Rev Neurosci 7:710–723

    Article  PubMed  CAS  Google Scholar 

  67. Philip N, Chabrol B, Lossi AM, Cardoso C, Guerrini R, Dobyns WB, Raybaud C, Villard L (2003) Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. J Med Genet 40:441–446

    Article  PubMed  CAS  Google Scholar 

  68. Purpura DP (1974) Dendritic spine “dysgenesis” and mental retardation. Science 186:1126–1128

    Article  PubMed  CAS  Google Scholar 

  69. Ramakers GJ (2002) Rho proteins, mental retardation and the cellular basis of cognition. Trends Neurosci 25:191–199

    Article  PubMed  CAS  Google Scholar 

  70. Riento K, Ridley AJ (2003) Rocks: multifunctional kinases in cell behaviour. Nat Rev Mol Cell Biol 4:446–456

    Article  PubMed  CAS  Google Scholar 

  71. Ropers HH, Hamel BC (2005) X-linked mental retardation. Nat Rev Genet 6:46–57

    Article  PubMed  CAS  Google Scholar 

  72. Sala C, Futai K, Yamamoto K, Worley PF, Hayashi Y, Sheng M (2003) Inhibition of dendritic spine morphogenesis and synaptic transmission by activity-inducible protein Homer1a. J Neurosci 23:6327–6337

    PubMed  CAS  Google Scholar 

  73. Sala C, Roussignol G, Meldolesi J, Fagni L (2005) Key role of the postsynaptic density scaffold proteins Shank and Homer in the functional architecture of Ca2+ homeostasis at dendritic spines in hippocampal neurons. J Neurosci 25:4587–4592

    Article  PubMed  CAS  Google Scholar 

  74. Schenck A, Bardoni B, Langmann C, Harden N, Mandel JL, Giangrande A (2003) CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein. Neuron 38:887–898

    Article  PubMed  CAS  Google Scholar 

  75. Soderling SH, Binns KL, Wayman GA, Davee SM, Ong SH, Pawson T, Scott JD (2002) The WRP component of the WAVE-1 complex attenuates Rac-mediated signalling. Nat Cell Biol 4:970–975

    Article  PubMed  CAS  Google Scholar 

  76. Soderling SH, Langeberg LK, Soderling JA, Davee SM, Simerly R, Raber J, Scott JD (2003) Loss of WAVE-1 causes sensorimotor retardation and reduced learning and memory in mice. Proc Natl Acad Sci USA 100:1723–1728

    Article  PubMed  CAS  Google Scholar 

  77. Takahashi H, Sekino Y, Tanaka S, Mizui T, Kishi S, Shirao T (2003) Drebrin-dependent actin clustering in dendritic filopodia governs synaptic targeting of postsynaptic density-95 and dendritic spine morphogenesis. J Neurosci 23:6586–6595

    PubMed  CAS  Google Scholar 

  78. Tashiro A, Yuste R (2004) Regulation of dendritic spine motility and stability by Rac1 and Rho kinase: evidence for two forms of spine motility. Mol Cell Neurosci 26:429–440

    Article  PubMed  CAS  Google Scholar 

  79. Tassabehji M, Metcalfe K, Fergusson WD, Carette MJ, Dore JK, Donnai D, Read AP, Proschel C, Gutowski NJ, Mao X, Sheer D (1996) LIM-kinase deleted in Williams syndrome. Nat Genet 13:272–273

    Article  PubMed  CAS  Google Scholar 

  80. Tentler D, Gustavsson P, Leisti J, Schueler M, Chelly J, Timonen E, Anneren G, Willard HF, Dahl N (1999) Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia. Eur J Hum Genet 7:541–548

    Article  PubMed  CAS  Google Scholar 

  81. Topp JD, Gray NW, Gerard RD, Horazdovsky BF (2004) Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor. J Biol Chem 279:24612–24623

    Article  PubMed  CAS  Google Scholar 

  82. Tudor EL, Perkinton MS, Schmidt A, Ackerley S, Brownlees J, Jacobsen NJ, Byers HL, Ward M, Hall A, Leigh PN, Shaw CE, McLoughlin DM, Miller CC (2005) ALS2/Alsin regulates Rac-PAK signaling and neurite outgrowth. J Biol Chem 280:34735–34740

    Article  PubMed  CAS  Google Scholar 

  83. Van Aelst L, D’Souza-Schorey C (1997) Rho GTPases and signaling networks. Genes Dev 11:2295–2322

    PubMed  Google Scholar 

  84. van Galen EJ, Ramakers GJ (2005) Rho proteins, mental retardation and the neurobiological basis of intelligence. Prog Brain Res 147:295–317

    Article  PubMed  CAS  Google Scholar 

  85. Wong K, Ren XR, Huang YZ, Xie Y, Liu G, Saito H, Tang H, Wen L, Brady- Kalnay SM, Mei L, Wu JY, Xiong WC, Rao Y (2001) Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway. Cell 107:209–221

    Article  PubMed  CAS  Google Scholar 

  86. Xiao B, Tu JC, Worley PF (2000) Homer: a link between neural activity and glutamate receptor function. Curr Opin Neurobiol 10:370–374

    Article  PubMed  CAS  Google Scholar 

  87. Yamanaka K, Vande Velde C, Eymard-Pierre E, Bertini E, Boespflug-Tanguy O, Cleveland DW (2003) Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease. Proc Natl Acad Sci USA 100:16041–16046

    Article  PubMed  CAS  Google Scholar 

  88. Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, Hentati F, Siddique T (2001) The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet 29:160–165

    Article  PubMed  CAS  Google Scholar 

  89. Yang Y, Marcello M, Endris V, Saffrich R, Fischer R, Trendelenburg MF, Sprengel R, Rappold G (2006) MEGAP impedes cell migration via regulating actin and microtubule dynamics and focal complex formation. Exp Cell Res 312:2379–2393

    Article  PubMed  CAS  Google Scholar 

  90. Yuste R, Bonhoeffer T (2001) Morphological changes in dendritic spines associated with long-term synaptic plasticity. Annu Rev Neurosci 24:1071–1089

    Article  PubMed  CAS  Google Scholar 

  91. Zanni G, Saillour Y, Nagara M, Billuart P, Castelnau L, Moraine C, Faivre L, Bertini E, Durr A, Guichet A, Rodriguez D, des Portes V, Beldjord C, Chelly J (2005) Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia. Neurology 65:1364–1369

    Article  PubMed  CAS  Google Scholar 

  92. Zhang H, Webb DJ, Asmussen H, Niu S, Horwitz AF (2005) A GIT1/PIX/Rac/PAK signaling module regulates spine morphogenesis and synapse formation through MLC. J Neurosci 25:3379–3388

    Article  PubMed  CAS  Google Scholar 

  93. Zhao L, Ma QL, Calon F, Harris-White ME, Yang F, Lim GP, Morihara T, Ubeda OJ, Ambegaokar S, Hansen JE, Weisbart RH, Teter B, Frautschy SA, Cole GM (2006) Role of p21-activated kinase pathway defects in the cognitive deficits of Alzheimer disease. Nat Neurosci 9:234–242

    Article  PubMed  CAS  Google Scholar 

  94. Zheng Y (2004) G protein control of microtubule assembly. Annu Rev Cell Dev Biol 20:867–894

    Article  PubMed  CAS  Google Scholar 

  95. Zito K, Knott G, Shepherd GM, Shenolikar S, Svoboda K (2004) Induction of spine growth and synapse formation by regulation of the spine actin cytoskeleton. Neuron 44:321–334

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

L.V.A is supported by the National Institutes of Health, National Science Foundation, and National Alliance for Autism Research. N.N.K is a postdoctoral fellow from the Fund for Scientific Research Flanders and is supported by the Human Frontiers Science Program.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Linda Van Aelst.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nadif Kasri, N., Van Aelst, L. Rho-linked genes and neurological disorders. Pflugers Arch - Eur J Physiol 455, 787–797 (2008). https://doi.org/10.1007/s00424-007-0385-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00424-007-0385-1

Keywords

Navigation