Literature DB >> 12384283

Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Ivan Conte1, Marta Lestingi, Anneke den Hollander, Maria Giuseppina Miano, Giovanna Alfano, Diego Circolo, Mariarosaria Pugliese, Francesco Testa, Francesca Simonelli, Ernesto Rinaldi, Montserrat Baiget, Sandro Banfi, Alfredo Ciccodicola.   

Abstract

Membrane-associated guanylate kinase (MAGUK) proteins are cell-cell contact organizing molecules that mediate targeting, clustering and anchoring of proteins at synapses and other cell junctions. MAGUK proteins may contain multiple protein-protein interaction motifs including PDZ, SH3 and guanylate kinase (GuK) domains. In this study, we performed a detailed analysis of the expression pattern of MPP4, a recently described member of the MAGUK protein family. We confirmed that this gene is highly expressed in retina, and demonstrate that it is also present, at lower levels, in brain. We identified a new retina specific isoform encoding a predicted protein lacking 71 amino acids. This protein region contains a newly identified L27 domain, another module playing a role in protein-protein interaction. By RNA in situ hybridization, Mpp4 expression was found to be localized to photoreceptor cells in postnatal retina. The MPP4 gene is localized to chromosome 2, in band 2q31-33, where a locus for autosomal recessive retinitis pigmentosa (RP26) has been mapped. Mutation analysis of the entire open reading frame of the MPP4 gene in a RP26 family revealed no pathologic mutations. In addition, we did not identify mutations in a panel of 300 unrelated patients with retinitis pigmentosa.

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Year:  2002        PMID: 12384283     DOI: 10.1016/s0378-1119(02)00872-7

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  5 in total

1.  Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.

Authors:  A Melamud; G-Q Shen; D Chung; Q Xi; E Simpson; L Li; N S Peachey; H Zegarra; S A Hagstrom; Q K Wang; E I Traboulsi
Journal:  J Med Genet       Date:  2006-06       Impact factor: 6.318

2.  The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy.

Authors:  Marcella Neri; Emanuele Valli; Giovanna Alfano; Matteo Bovolenta; Pietro Spitali; Claudio Rapezzi; Francesco Muntoni; Sandro Banfi; Giovanni Perini; Francesca Gualandi; Alessandra Ferlini
Journal:  BMC Med Genet       Date:  2012-03-28       Impact factor: 2.103

3.  Demethylation of miR-34a upregulates expression of membrane palmitoylated proteins and promotes the apoptosis of liver cancer cells.

Authors:  Fu-Yong Li; Ting-Yong Fan; Hao Zhang; Yu-Min Sun
Journal:  World J Gastroenterol       Date:  2021-02-14       Impact factor: 5.742

4.  The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.

Authors:  Ivana Peluso; Ivan Conte; Francesco Testa; Gopuraja Dharmalingam; Mariateresa Pizzo; Rob W J Collin; Nicola Meola; Sara Barbato; Margherita Mutarelli; Carmela Ziviello; Anna Maria Barbarulo; Vincenzo Nigro; Mariarosa A B Melone; Francesca Simonelli; Sandro Banfi
Journal:  Orphanet J Rare Dis       Date:  2013-01-28       Impact factor: 4.123

5.  On the role of the MAGUK proteins encoded by Drosophila varicose during embryonic and postembryonic development.

Authors:  André Bachmann; Margarete Draga; Ferdi Grawe; Elisabeth Knust
Journal:  BMC Dev Biol       Date:  2008-05-18       Impact factor: 1.978

  5 in total

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