Literature DB >> 7550318

Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice.

M Toth1, J Grimsby, G Buzsaki, G P Donovan.   

Abstract

Epidemiological data and genetic studies indicate that certain forms of human epilepsy are inherited. Based on the similarity between the human and mouse genomes, mouse models of epilepsy could facilitate the discovery of genes associated with epilepsy syndromes. Here, we report an insertional murine mutation that inactivates a novel gene and results in whole body jerks, generalized clonic seizures, and epileptic brain activity in transgenic mice. The gene, named jerky, encodes a putative 41.7 kD protein displaying homology to a number of nuclear regulatory proteins, suggesting that perhaps the jerky protein is able to bind DNA.

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Year:  1995        PMID: 7550318     DOI: 10.1038/ng0995-71

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  28 in total

1.  The RNA binding domain of Jerky consists of tandemly arranged helix-turn-helix/homeodomain-like motifs and binds specific sets of mRNAs.

Authors:  Wencheng Liu; Jeremy Seto; Etienne Sibille; Miklos Toth
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

Review 2.  Transposable elements as drivers of genomic and biological diversity in vertebrates.

Authors:  Astrid Böhne; Frédéric Brunet; Delphine Galiana-Arnoux; Christina Schultheis; Jean-Nicolas Volff
Journal:  Chromosome Res       Date:  2008       Impact factor: 5.239

3.  Jerky, a protein deficient in a mouse epilepsy model, is associated with translationally inactive mRNA in neurons.

Authors:  Wencheng Liu; Jeremy Seto; Gerald Donovan; Miklos Toth
Journal:  J Neurosci       Date:  2002-01-01       Impact factor: 6.167

4.  Members of the pogo superfamily of DNA-mediated transposons in the human genome.

Authors:  H M Robertson
Journal:  Mol Gen Genet       Date:  1996-10-28

5.  Functional redundancies, distinct localizations and interactions among three fission yeast homologs of centromere protein-B.

Authors:  J T Irelan; G I Gutkin; L Clarke
Journal:  Genetics       Date:  2001-03       Impact factor: 4.562

Review 6.  Deficiency in protein L-isoaspartyl methyltransferase results in a fatal progressive epilepsy.

Authors:  A Yamamoto; H Takagi; D Kitamura; H Tatsuoka; H Nakano; H Kawano; H Kuroyanagi; Y Yahagi; S Kobayashi; K Koizumi; T Sakai; K Saito; T Chiba; K Kawamura; K Suzuki; T Watanabe; H Mori; T Shirasawa
Journal:  J Neurosci       Date:  1998-03-15       Impact factor: 6.167

7.  Fission yeast homologs of human CENP-B have redundant functions affecting cell growth and chromosome segregation.

Authors:  M Baum; L Clarke
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

8.  Disturbed Prefrontal Cortex Activity in the Absence of Schizophrenia-Like Behavioral Dysfunction in Arc/Arg3.1 Deficient Mice.

Authors:  Xiaoyan Gao; Jasper Grendel; Mary Muhia; Sergio Castro-Gomez; Ute Süsens; Dirk Isbrandt; Matthias Kneussel; Dietmar Kuhl; Ora Ohana
Journal:  J Neurosci       Date:  2019-09-05       Impact factor: 6.167

9.  PCNA binding proteins in Drosophila melanogaster : the analysis of a conserved PCNA binding domain.

Authors:  E Warbrick; W Heatherington; D P Lane; D M Glover
Journal:  Nucleic Acids Res       Date:  1998-09-01       Impact factor: 16.971

10.  Inherent promoter bidirectionality facilitates maintenance of sequence integrity and transcription of parasitic DNA in mammalian genomes.

Authors:  Paul Kalitsis; Richard Saffery
Journal:  BMC Genomics       Date:  2009-10-27       Impact factor: 3.969

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