Genetic analysis of cerebellar folial pattern in crosses of C57BL/6J and DBA/2J inbred mice

Paul E. Neumann, John D. Garretson, George P. Skabardonis, Gary G. Mueller

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25 Citations (Scopus)

Abstract

Variation in the cerebellar folial pattern of mice is influenced by genetic elements [Inouye, M. and Oda, S., J. Comp. Neurol., 190 (1980) 357-362]. In crosses of C57BL/6J and DBA/2J inbred mice, the presence or absence of a specific fissure, the intraculminate fissure, is largely determined by a single genetic locus (Cfp-1), which is located on distal Chromosome 4 [Neumann et al., Brain Res., 524 (1990) 85-89]. In the present study, the mid-sagittal cerebellar folial pattern has been examined in crosses of C57BL/6J and DBA/2J mice and in BXD recombinant inbred strains. At least three loci, including Cfp-1, are involved in variation in vermian pattern formation. Genetic variation in thyroid hormone function may be involved in the inheritance of folial pattern. A locus (Cfp-2) that appears to be partially responsible for this negative genetic correlation in mice may be linked to Afp on Chromosome 5. This hypothesis was suggested by the negative correlation between neonatal serum T4 level and the number of folia in rats given neonatal injections of thyroxine or propylthiouracil [Lauder, J.M. et al., Brain Res., 76 (1974) 33-40].

Original languageEnglish
Pages (from-to)81-88
Number of pages8
JournalBrain Research
Volume619
Issue number1-2
DOIs
Publication statusPublished - Aug 13 1993
Externally publishedYes

Bibliographical note

Funding Information:
Acknowledgements. This manuscript is dedicated to Dr. Charles Barlow on the occasion of his retirement from the Bronson Crothers Professorship (Harvard Medical School) for his support of this project. The authors thank Dr. Wim E. Crusio for providing a traditional quantitative genetic analysis of the classical cross data and Drs. Donald Bailey, Larry Benowitz, Merton Bernfield, Robert Collins, Wim Crnsio, Scott Pomeroy, Lydia Villa-Komaroff and Lewis Wolpert for critical readings of various drafts of the manuscript. The work was supported in part by Children's Hospital and the Public Health Service (N01-HD-02912, P30-HD18655, P30-HD-27805 and UO1-HD-28882). Children's Hospital is fully accredited by the American Association for Accreditation of Laboratory Animal Care.

ASJC Scopus Subject Areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

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