Glucocorticoid Inhibition of RNA Synthesis Responsible for Cleft Palate in Mice: A Model
Author(s) -
Ernest F. Zimmerman,
F. D. Andrew,
Harold Kalter
Publication year - 1970
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.67.2.779
Subject(s) - cycloheximide , protein biosynthesis , glucocorticoid , triamcinolone acetonide , messenger rna , rna , endocrinology , medicine , chemistry , microbiology and biotechnology , biology , biochemistry , immunology , gene
A study was undertaken to elucidate the molecular mechanisms by which glucocorticoids induce cleft palate in mice. It was hypothesized that a compound such as triamcinolone acetonide inhibits mRNA synthesis; that this results later in depressed protein synthesis; and that the latter is ultimately responsible for slowed palate formation and cleft palate. Support for the model derives from the fact that the palatine shelves rise and fuse 3-4 days after the most sensitive time of administration of steroid; RNA synthesis was markedly inhibited 6-24 hr after its administration; and coadministration of cycloheximide partially reversed the tendency toward cleft palate formation.
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