Literature DB >> 10671314

General or cell type-specific deletion and replacement of connexin-coding DNA in the mouse.

M Theis1, T M Magin, A Plum, K Willecke.   

Abstract

Here we describe several gene targeting approaches currently used in our laboratory for the generation of deletion or replacement mutants of connexin genes in the mouse and discuss the advantage of the double-replacement strategy for the generation of conditional mutants. For the analysis of complementary functions of connexins, it will be necessary to generate mice with mutations in several connexin genes. We also report how this can be effectively accomplished. The replacement of targeted connexin-coding DNA with a reporter gene, to mimic expression of the deleted gene product, is currently being used in several laboratories. The use of different reporter genes or their differently localized gene products could allow distinction of promoter activity in double or triple connexin mutant mice. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10671314     DOI: 10.1006/meth.1999.0938

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  10 in total

1.  Deletion of connexin45 in mouse retinal neurons disrupts the rod/cone signaling pathway between AII amacrine and ON cone bipolar cells and leads to impaired visual transmission.

Authors:  Stephan Maxeiner; Karin Dedek; Ulrike Janssen-Bienhold; Josef Ammermüller; Hendrik Brune; Taryn Kirsch; Mario Pieper; Joachim Degen; Olaf Krüger; Klaus Willecke; Reto Weiler
Journal:  J Neurosci       Date:  2005-01-19       Impact factor: 6.167

2.  Visual transmission deficits in mice with targeted disruption of the gap junction gene connexin36.

Authors:  M Güldenagel; J Ammermüller; A Feigenspan; B Teubner; J Degen; G Söhl; K Willecke; R Weiler
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

3.  The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.

Authors:  Melanie Schütz; Pietro Scimemi; Paromita Majumder; Romolo Daniele De Siati; Giulia Crispino; Laura Rodriguez; Mario Bortolozzi; Rosamaria Santarelli; Anke Seydel; Stephan Sonntag; Neil Ingham; Karen P Steel; Klaus Willecke; Fabio Mammano
Journal:  Hum Mol Genet       Date:  2010-09-21       Impact factor: 6.150

4.  The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.

Authors:  Radoslaw Dobrowolski; Philipp Sasse; Jan W Schrickel; Marcus Watkins; Jung-Sun Kim; Mindaugas Rackauskas; Clemens Troatz; Alexander Ghanem; Klaus Tiemann; Joachim Degen; Feliksas F Bukauskas; Roberto Civitelli; Thorsten Lewalter; Bernd K Fleischmann; Klaus Willecke
Journal:  Hum Mol Genet       Date:  2007-11-13       Impact factor: 6.150

5.  A sertoli cell-specific knockout of connexin43 prevents initiation of spermatogenesis.

Authors:  Ralph Brehm; Martina Zeiler; Christina Rüttinger; Katja Herde; Mark Kibschull; Elke Winterhager; Klaus Willecke; Florian Guillou; Charlotte Lécureuil; Klaus Steger; Lutz Konrad; Katharina Biermann; Klaus Failing; Martin Bergmann
Journal:  Am J Pathol       Date:  2007-07       Impact factor: 4.307

6.  Effects of a murine germ cell-specific knockout of Connexin 43 on Connexin expression in testis and fertility.

Authors:  Sabine Günther; Daniela Fietz; Karola Weider; Martin Bergmann; Ralph Brehm
Journal:  Transgenic Res       Date:  2012-11-28       Impact factor: 2.788

7.  Localization of neurones expressing the gap junction protein Connexin45 within the adult spinal dorsal horn: a study using Cx45-eGFP reporter mice.

Authors:  R J Chapman; V K Lall; S Maxeiner; K Willecke; J Deuchars; A E King
Journal:  Brain Struct Funct       Date:  2012-05-26       Impact factor: 3.270

8.  Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.

Authors:  Oliver Tress; Marta Maglione; Armin Zlomuzica; Dennis May; Nikolai Dicke; Joachim Degen; Ekrem Dere; Helmut Kettenmann; Dieter Hartmann; Klaus Willecke
Journal:  PLoS Genet       Date:  2011-07-07       Impact factor: 5.917

9.  Establishment and functional characterization of a murine primary Sertoli cell line deficient of connexin43.

Authors:  Jonathan Gerber; Kristina Rode; Nina Hambruch; Marion Langeheine; Nadine Schnepel; Ralph Brehm
Journal:  Cell Tissue Res       Date:  2020-04-23       Impact factor: 5.249

10.  Loss of Cx43 in Murine Sertoli Cells Leads to Altered Prepubertal Sertoli Cell Maturation and Impairment of the Mitosis-Meiosis Switch.

Authors:  Erika Hilbold; Ottmar Distl; Martina Hoedemaker; Sandra Wilkening; Rüdiger Behr; Aleksandar Rajkovic; Marion Langeheine; Kristina Rode; Klaus Jung; Julia Metzger; Ralph H J Brehm
Journal:  Cells       Date:  2020-03-10       Impact factor: 6.600

  10 in total

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