Literature DB >> 19224308

Pogo: a novel spontaneous ataxic mutant mouse.

Nam-Seob Lee1, Young-Gil Jeong.   

Abstract

The Pogo (pogo/pogo) mouse is a naturally occurring neurological mutant from a Korean wild-type mouse characterized by loss of balance and motor coordination due to dysfunction of the cerebellum. The Pogo mutation is believed to be an allele of P/Q-type calcium channel mutants such as tottering, leaner, and rolling mouse Nagoya. These mutants have been served as mouse models for a group of neurodegenerative diseases. The overall aim of this minireview is to summarize our current understanding of the ataxic Pogo mouse. To address this issue, we first describe the discovery of Pogo mouse and its morphological and behavioral defects. Then, we focus on the abnormal expression of several molecules in the Pogo cerebellum, including tyrosine hydroxylase, glutamate, corticotrophin-releasing factor, and 5-hydroxytryptamine. Much of this review is concerned with the functional implications of these ectopic molecules in the Pogo cerebellum.

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Year:  2009        PMID: 19224308     DOI: 10.1007/s12311-009-0096-6

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  51 in total

1.  Purkinje cell degeneration, a new neurological mutation in the mouse.

Authors:  R J Mullen; E M Eicher; R L Sidman
Journal:  Proc Natl Acad Sci U S A       Date:  1976-01       Impact factor: 11.205

2.  [Simultaneous resolution and determination of tyrosine, tryptophan and phenylalanine by alternating penalty trilinear decomposition algorithm coupled with 3D emission-excitation matrix fluorometry].

Authors:  Jin Xiao; Feng-lian Ren; Ge Song; Lü Liao; Wen-feng Yu; Tao Zeng
Journal:  Guang Pu Xue Yu Guang Pu Fen Xi       Date:  2007-10       Impact factor: 0.589

3.  Chromosomal localization of the neurological mouse mutations tottering (tg), Purkinje cell degeneration (pcd), and nervous (nr).

Authors:  D B Campbell; E J Hess
Journal:  Brain Res Mol Brain Res       Date:  1996-04

4.  An ultrastructural study of granule cell/Purkinje cell synapses in tottering (tg/tg), leaner (tg(la)/tg(la)) and compound heterozygous tottering/leaner (tg/tg(la)) mice.

Authors:  I J Rhyu; L C Abbott; D B Walker; C Sotelo
Journal:  Neuroscience       Date:  1999-03       Impact factor: 3.590

5.  Promoter elements and second messenger pathways involved in transcriptional activation of tyrosine hydroxylase by ionomycin.

Authors:  B Nankova; B Hiremagalur; A Menezes; R Zeman; E Sabban
Journal:  Brain Res Mol Brain Res       Date:  1996-01

6.  Bidirectional alterations in cerebellar synaptic transmission of tottering and rolling Ca2+ channel mutant mice.

Authors:  Kaori Matsushita; Minoru Wakamori; Im Joo Rhyu; Tatsuo Arii; Sen-Ichi Oda; Yasuo Mori; Keiji Imoto
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

7.  Three syndromes produced by two mutant genes in the mouse. Clinical, pathological, and ultrastructural bases of tottering, leaner, and heterozygous mice.

Authors:  H Meier; A D MacPike
Journal:  J Hered       Date:  1971 Sep-Oct       Impact factor: 2.645

8.  Neurotransmitter abnormality in Rolling mouse Nagoya, an ataxic mutant mouse.

Authors:  O Muramoto; I Kanazawa; K Ando
Journal:  Brain Res       Date:  1981-06-29       Impact factor: 3.252

9.  Cyclin-dependent kinase 5 phosphorylates serine 31 of tyrosine hydroxylase and regulates its stability.

Authors:  Lily Y Moy; Li-Huei Tsai
Journal:  J Biol Chem       Date:  2004-10-07       Impact factor: 5.157

10.  Tyrosine hydroxylase expression and Cdk5 kinase activity in ataxic cerebellum.

Authors:  K-John J Cheung; Jesusa L Rosales; Byung-Chul Lee; Young-Gil Jeong; Ki-Young Lee
Journal:  Mol Cell Biochem       Date:  2008-07-10       Impact factor: 3.396

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  3 in total

1.  Animal models of human cerebellar ataxias: a cornerstone for the therapies of the twenty-first century.

Authors:  Mario Manto; Daniele Marmolino
Journal:  Cerebellum       Date:  2009-09       Impact factor: 3.847

2.  Motor learning of mice lacking cerebellar Purkinje cells.

Authors:  M Elena Porras-García; Rocío Ruiz; Eva M Pérez-Villegas; José Á Armengol
Journal:  Front Neuroanat       Date:  2013-04-23       Impact factor: 3.856

3.  Protein expression pattern in cerebellum of Cav2.1 mutant, tottering-6j mice.

Authors:  Tae Yeon Kim; Kimie Niimi; Eiki Takahashi
Journal:  Exp Anim       Date:  2016-02-17
  3 in total

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