Literature DB >> 12379762

The myelin vacuolation (mv) rat with a null mutation in the attractin gene.

Mitsuru Kuwamura1, Masaya Maeda, Takashi Kuramoto, Kazuhiro Kitada, Toshiko Kanehara, Mitsuaki Moriyama, Yoshifumi Nakane, Jyoji Yamate, Toshikazu Ushijima, Takao Kotani, Tadao Serikawa.   

Abstract

We recently found a spontaneous tremor mutant in an outbred colony of Sprague-Dawley rats. The tremor behavior was exhibited from around 3 weeks of age and inherited as an autosomal recessive trait. The mutant rats had variously sized vacuoles in the neuropil and white matter throughout the central nervous system, especially in the brain stem, cerebellum, and spinal cord. Ultrastructurally these vacuoles mainly consisted of splitting of myelin lamella both in the periaxonal and intermyelinic spaces. Linkage analysis using intercross progeny between the myelin vacuolation (mv) rat, named after the pathologic characteristics, and normal control rat strains showed that the mv phenotypes were cosegregated with polymorphic markers adjacent to the Atrn (Attractin, formerly zi [zitter]) locus on rat chromosome 3. A test for allelism suggested that the mv mutation was a new allele in ATRN: In comparison with a marked decrease of Atrn(zi)/Arn(zi), Northern blot analysis revealed no expression of Atrn mRNA in the brain of the mv rats. Finally, a genomic deletion including exon 1 of the mv rats was detected by genomic and sequence analyses. Discovery of the rat null mutation Atrn(mv), different from Atrn(zi), provides a new animal model for studying the functions of the attractin protein.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12379762     DOI: 10.1097/01.lab.0000032375.70196.26

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  8 in total

Review 1.  Rat models of human diseases and related phenotypes: a systematic inventory of the causative genes.

Authors:  Claude Szpirer
Journal:  J Biomed Sci       Date:  2020-08-02       Impact factor: 8.410

2.  Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein.

Authors:  Andrea M Haqq; Patricia René; Toshiro Kishi; Kathy Khong; Charlotte E Lee; Hongyan Liu; Jeffrey M Friedman; Joel K Elmquist; Roger D Cone
Journal:  Biochem J       Date:  2003-12-15       Impact factor: 3.857

3.  SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F.

Authors:  Fatma Ayhan; Barbara A Perez; Hannah K Shorrock; Tao Zu; Monica Banez-Coronel; Tammy Reid; Hirokazu Furuya; H Brent Clark; Juan C Troncoso; Christopher A Ross; S H Subramony; Tetsuo Ashizawa; Eric T Wang; Anthony T Yachnis; Laura Pw Ranum
Journal:  EMBO J       Date:  2018-09-11       Impact factor: 11.598

4.  Attractin gene deficiency contributes to testis vacuolization and sperm dysfunction in male mice.

Authors:  Jie Li; Shiqi Wang; Shiyun Huang; Dan Cheng; Shiliang Shen; Chengliang Xiong
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2009-12-29

5.  Enhanced Expression of Trib3 during the Development of Myelin Breakdown in dmy Myelin Mutant Rats.

Authors:  Yukako Shimotsuma; Miyuu Tanaka; Takeshi Izawa; Jyoji Yamate; Mitsuru Kuwamura
Journal:  PLoS One       Date:  2016-12-15       Impact factor: 3.240

6.  Post-developmental extracellular proteoglycan maintenance in attractin-deficient mice.

Authors:  Abdallah Azouz; Jonathan S Duke-Cohan
Journal:  BMC Res Notes       Date:  2020-06-24

7.  Non-cell autonomous impairment of oligodendrocyte differentiation precedes CNS degeneration in the Zitter rat: implications of macrophage/microglial activation in the pathogenesis.

Authors:  Shin-ichi Sakakibara; Kazuhiko Nakadate; Shigeo Ookawara; Shuichi Ueda
Journal:  BMC Neurosci       Date:  2008-04-05       Impact factor: 3.288

Review 8.  Inherited and acquired disorders of myelin: The underlying myelin pathology.

Authors:  Ian D Duncan; Abigail B Radcliff
Journal:  Exp Neurol       Date:  2016-04-09       Impact factor: 5.330

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.