Literature DB >> 21445960

The spatio-temporal expression of ProSAP/shank family members and their interaction partner LAPSER1 during Xenopus laevis development.

Susanne Gessert1, Michael J Schmeisser, Si Tao, Tobias M Boeckers, Michael Kühl.   

Abstract

Members of the ProSAP/Shank family are important scaffolding proteins of the postsynaptic density (PSD). We investigated for the first time the expression of the three family members named Shank1, ProSAP1/Shank2, and ProSAP2/Shank3 during Xenopus laevis development. Shank1 is expressed in the neural tube, the retina, and the cranial ganglions. In contrast, ProSAP1/Shank2 transcripts could be visualized in the otic vesicle, the pronephros, the liver, the neural tube, and the retina. ProSAP2/Shank3 could be detected in the cardiovascular network, the neural tube, the pronephros, and the retina. Furthermore, we showed that LAPSER1 interacts with all three ProSAP/Shank family members in Xenopus embryos and co-localizes with ProSAP/Shank in a cell-based assay. In Xenopus, LAPSER1 is expressed in somites, brain, proctodeum, pronephros, and in some cranial ganglions. Thus, we suggest that members of the ProSAP/Shank family and LAPSER1 not only play a role in PSD formation and plasticity, but also during embryonic development.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21445960     DOI: 10.1002/dvdy.22613

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  7 in total

1.  Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.

Authors:  Robert A Kozol; Holly N Cukier; Bing Zou; Vera Mayo; Silvia De Rubeis; Guiqing Cai; Anthony J Griswold; Patrice L Whitehead; Jonathan L Haines; John R Gilbert; Michael L Cuccaro; Eden R Martin; James D Baker; Joseph D Buxbaum; Margaret A Pericak-Vance; Julia E Dallman
Journal:  Hum Mol Genet       Date:  2015-04-16       Impact factor: 6.150

2.  Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.

Authors:  Daniela M Cochoy; Alexander Kolevzon; Yuji Kajiwara; Michael Schoen; Maria Pascual-Lucas; Stacey Lurie; Joseph D Buxbaum; Tobias M Boeckers; Michael J Schmeisser
Journal:  Mol Autism       Date:  2015-04-29       Impact factor: 7.509

3.  Stem cell-derived neurons from autistic individuals with SHANK3 mutation show morphogenetic abnormalities during early development.

Authors:  A Kathuria; P Nowosiad; R Jagasia; S Aigner; R D Taylor; L C Andreae; N J F Gatford; W Lucchesi; D P Srivastava; J Price
Journal:  Mol Psychiatry       Date:  2017-09-26       Impact factor: 15.992

4.  Expression of SH3 and Multiple Ankyrin Repeat Domains Protein 3 in Mouse Retina.

Authors:  Yue Xu; Ya'nan Wang; Guang'an Tong; Lin Li; Juan Cheng; Lesha Zhang; Qi Xu; Liecheng Wang; Pingping Zhang
Journal:  Front Cell Neurosci       Date:  2022-03-25       Impact factor: 5.505

5.  Association of shank 1A scaffolding protein with cone photoreceptor terminals in the mammalian retina.

Authors:  Salvatore L Stella; Alejandro Vila; Albert Y Hung; Michael E Rome; Uyenchi Huynh; Morgan Sheng; Hans-Juergen Kreienkamp; Nicholas C Brecha
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

Review 6.  Modeling human neurodevelopmental disorders in the Xenopus tadpole: from mechanisms to therapeutic targets.

Authors:  Kara G Pratt; Arseny S Khakhalin
Journal:  Dis Model Mech       Date:  2013-08-07       Impact factor: 5.758

7.  The Nedd4-binding protein 3 (N4BP3) is crucial for axonal and dendritic branching in developing neurons.

Authors:  Michael J Schmeisser; Susanne J Kühl; Michael Schoen; Nathalie H Beth; Tobias M Weis; Andreas M Grabrucker; Michael Kühl; Tobias M Boeckers
Journal:  Neural Dev       Date:  2013-09-17       Impact factor: 3.842

  7 in total

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