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Mol. Cell. Biol., 04 1996, 1794-1804, Vol 16, No. 4
KS Hatton, K Mahon, L Chin, FC Chiu, HW Lee, D Peng, SD Morgenbesser, J Horner and RA DePinho
To determine the role of L-Myc in normal mammalian development and its
functional relationship to other members of the Myc family, we determined
the normal patterns of L-myc gene expression in the developing mouse by RNA
in situ hybridization and assessed the phenotypic impact of L-Myc
deficiency produced through standard gene targeting methodology. L-myc
transcripts were detected in the developing kidney and lung as well as in
both the proliferative and the differentiative zones of the brain and
neural tube. Despite significant expression of L-myc in developing mouse
tissue, homozygous null L-myc mice were found to be viable, reproductively
competent, and represented in expected frequencies from heterozygous
matings. A detailed histological survey of embryonic and adult tissues,
characterization of an embryonic neuronal marker, and measurement of
cellular proliferation in situ did not reveal any congenital abnormalities.
The lack of an apparent phenotype associated with L-Myc deficiency
indicates that L- Myc is dispensable for gross morphological development
and argues against a unique role for L-Myc in early central nervous system
development as had been previously suggested. Although overlapping
expression patterns among myc family members raise the possibility of
complementation of L-Myc deficiency by other Myc oncoproteins, compensatory
changes in the levels of c- and/or N-myc transcripts were not detected in
homozygous null L-myc mice.
Copyright © 1996, American Society for Microbiology
Expression and activity of L-Myc in normal mouse development
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
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