Oligophrenin-1, a Rho GTPase-activating protein (RhoGAP) involved in X-linked mental retardation, is expressed in the enteric nervous system.

Oligophrenin-1 is a RhoGTPase-activating protein (RhoGAP) that is involved in the regulation of shape changes in dendritic spines, and outgrowth of axons and dendrites in the brain. These changes in neuronal morphology are central to the mechanisms of plasticity, learning, and memory. Although the enteric nervous system also exhibits long-term changes in neuronal function, the expression and involvement of oligophrenin-1 has not previously been investigated. We show by RT-PCR analysis that oligophrenin-1 mRNA is expressed in the myenteric plexus (MP) of the guinea pig ileum. Sequencing of RT-PCR products showed that guinea pig oligophrenin-1 mRNA is 98% and 87% homologous to human and mouse oligophrenin-1, respectively, except that a 42 bp sequence is absent from the guinea pig mRNA. This 42 bp sequence codes for a sequence of 14 amino acids located near the carboxy-terminal end of the RhoGAP domain in the human sequence. An antibody that recognizes human oligophrenin-1 identified a 91 kDa protein band in rat and mouse brain lysates and in guinea pig sciatic nerve, and a 36 kDa protein band in both purified enteric ganglion cell and brain lysate from guinea pig. Oligophrenin-1 is localized specifically to neurons and varicose axons in the MPs and submucosal plexuses (SMPs) of the guinea pig and rat, but is not detectable in glial cells, smooth muscle, or other cell types. These findings indicate that oligophrenin-1 is expressed in the enteric nervous system, where it may regulate morphological changes in axons and dendrites, and thus modulate neuronal connectivity.

[1]  Z. Lin,et al.  Immunoreactivity of Hu proteins facilitates identification of myenteric neurones in guinea‐pig small intestine , 2002, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

[2]  Ger J. A. Ramakers,et al.  Rho proteins, mental retardation and the cellular basis of cognition , 2002, Trends in Neurosciences.

[3]  O. Caballero,et al.  Significant overexpression of oligophrenin-1 in colorectal tumors detected by cDNA microarray analysis. , 2001, Cancer letters.

[4]  N. M. Khazenzon,et al.  Gene expression abnormalities in human glial tumors identified by gene array. , 2001, International journal of oncology.

[5]  L. Luo RHO GTPASES in neuronal morphogenesis , 2000, Nature Reviews Neuroscience.

[6]  P. Billuart,et al.  Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation. , 2000, Annales de genetique.

[7]  F. Ponti,et al.  Plasticity in the enteric nervous system. , 1999, Gastroenterology.

[8]  H. Willard,et al.  Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia , 1999, European Journal of Human Genetics.

[9]  P. Holzer Implications of Tachykinins and Calcitonin Gene-Related Peptide in Inflammatory Bowel Disease , 1998, Digestion.

[10]  H. R. Crollius,et al.  Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation , 1998, Nature.

[11]  A. Hall,et al.  Rho GTPases and the actin cytoskeleton. , 1998, Science.

[12]  C. Kenyon,et al.  Role of a New Rho Family Member in Cell Migration and Axon Guidance in C. elegans , 1997, Cell.

[13]  Richard Threadgill,et al.  Regulation of Dendritic Growth and Remodeling by Rho, Rac, and Cdc42 , 1997, Neuron.

[14]  R. Stevenson,et al.  Study of X-linked mental retardation (XLMR): summary of 61 families in the Miami/Greenwood Study. , 1996, American journal of medical genetics.

[15]  Y. Jan,et al.  Differential effects of the Rac GTPase on Purkinje cell axons and dendritic trunks and spines , 1996, Nature.

[16]  Y. Jan,et al.  Distinct morphogenetic functions of similar small GTPases: Drosophila Drac1 is involved in axonal outgrowth and myoblast fusion. , 1994, Genes & development.

[17]  J. Rostas,et al.  Protein phosphorylation in guinea-pig myenteric ganglia and brain: Presence of calmodulin kinase II, protein kinase C and cyclic AMP kinase and characterization of major phosphoproteins , 1991, Neuroscience.

[18]  G. Gabella On the plasticity of form and structure of enteric ganglia. , 1990, Journal of the autonomic nervous system.

[19]  J. Galligan,et al.  Substance P mediates neurogenic vasodilatation in extrinsically denervated guinea‐pig submucosal arterioles. , 1990, The Journal of physiology.

[20]  M. Costa,et al.  Migration of the myoelectric complex after interruption of the myenteric plexus: intestinal transection and regeneration of enteric nerves in the guinea pig. , 1989, Gastroenterology.

[21]  G. Gabella Size of neurons and glial cells in the intramural ganglia of the hypertrophic intestine of the guinea-pig , 1984, Journal of neurocytology.

[22]  S. Sarna,et al.  Enteric mechanisms of initiation of migrating myoelectric complexes in dogs. , 1983, Gastroenterology.