Literature DB >> 3429842

Spasmodic, a mutation on chromosome 11 in the mouse.

P W Lane1, A L Ganser, A L Kerner, W F White.   

Abstract

A new recessive mutation, spasmodic (spd), producing behavior that mimics that of the neurological mutation spastic (spa) with rapid tremors, stiff posture, and difficulty in righting, arose spontaneously in strain A/HeJ at the Jackson Laboratory in 1979. It is not an allele of spa and linkage tests show that this mutation is located close to vestigial tail (vt) near the center of chromosome 11. Additional genetic tests show that it is not an allele of trembler (Tr), shaker-2 (sh-2), nor vibrator (vb), all neurological mutations located in the same region of chromosome 11. No differences were observed in the levels of the major CNS and PNS myelin proteins or lipids of spd/spd mice versus littermate controls, suggesting that, unlike several closely linked mutations, the spd mutation does not affect myelination. Pharmacological studies reported here show that aminooxyacetic acid improves the behavioral abnormalities of affected spd/spd mice in the same way it improves the behavior of affected spa/spa mice. However, unlike the spa/spa mice, there are no changes in the postsynaptic receptors for glycine, GABA, or benzodiazepines in spd/spd mice.

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Year:  1987        PMID: 3429842     DOI: 10.1093/oxfordjournals.jhered.a110414

Source DB:  PubMed          Journal:  J Hered        ISSN: 0022-1503            Impact factor:   2.645


  11 in total

Review 1.  Mouse chromosome 11.

Authors:  A M Buchberg; M S Buckwalter; S A Camper
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 11.

Authors:  A M Buchberg; J J Moskow; M S Buckwalter; S A Camper
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Probing glycine receptor stoichiometry in superficial dorsal horn neurones using the spasmodic mouse.

Authors:  B A Graham; M A Tadros; P R Schofield; R J Callister
Journal:  J Physiol       Date:  2011-03-08       Impact factor: 5.182

4.  Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.

Authors:  P Gregor; R H Reeves; E W Jabs; X Yang; W Dackowski; J M Rochelle; R H Brown; J L Haines; B F O'Hara; G R Uhl
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-01       Impact factor: 11.205

5.  Molecular cloning and chromosomal localization of one of the human glutamate receptor genes.

Authors:  C Puckett; C M Gomez; J R Korenberg; H Tung; T J Meier; X N Chen; L Hood
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

6.  Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.

Authors:  D H Ledbetter; S A Ledbetter; P vanTuinen; K M Summers; T J Robinson; Y Nakamura; R Wolff; R White; D F Barker; M R Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

7.  Single-channel study of the spasmodic mutation alpha1A52S in recombinant rat glycine receptors.

Authors:  Andrew J R Plested; Paul J Groot-Kormelink; David Colquhoun; Lucia G Sivilotti
Journal:  J Physiol       Date:  2007-03-01       Impact factor: 5.182

8.  Glycine receptor mutants of the mouse: what are possible routes of inhibitory compensation?

Authors:  Natascha Schaefer; Nicolas Vogel; Carmen Villmann
Journal:  Front Mol Neurosci       Date:  2012-10-31       Impact factor: 5.639

9.  Murine startle mutant Nmf11 affects the structural stability of the glycine receptor and increases deactivation.

Authors:  Megan E Wilkins; Alex Caley; Marc C Gielen; Robert J Harvey; Trevor G Smart
Journal:  J Physiol       Date:  2016-05-10       Impact factor: 5.182

Review 10.  Synaptopathies: synaptic dysfunction in neurological disorders - A review from students to students.

Authors:  Katarzyna Lepeta; Mychael V Lourenco; Barbara C Schweitzer; Pamela V Martino Adami; Priyanjalee Banerjee; Silvina Catuara-Solarz; Mario de La Fuente Revenga; Alain Marc Guillem; Mouna Haidar; Omamuyovwi M Ijomone; Bettina Nadorp; Lin Qi; Nirma D Perera; Louise K Refsgaard; Kimberley M Reid; Mariam Sabbar; Arghyadip Sahoo; Natascha Schaefer; Rebecca K Sheean; Anna Suska; Rajkumar Verma; Cinzia Vicidomini; Dean Wright; Xing-Ding Zhang; Constanze Seidenbecher
Journal:  J Neurochem       Date:  2016-09-08       Impact factor: 5.372

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