Molecular basis of the little mouse phenotype and Implications for cell type-specific growth
- 1 July 1993
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 364 (6434) , 208-213
- https://doi.org/10.1038/364208a0
Abstract
The molecular basis for the little (lit) mouse phenotype, characterized by a hypoplastic anterior pituitary gland, is the mutation of a single nucleotide that alters Asp 60 to Gly in the growth hormone releasing factor receptor. Detailed analysis of the lit mouse anterior pituitary reveals spatially distinct proliferative zones of growth hormone-producing stem cells and mature somatotrophs, each regulated by a different trophic factor. This sequential growth factor requirement for a specific cell type may exemplify a common strategy for regulating cellular proliferation in other mammalian organs.Keywords
This publication has 49 references indexed in Scilit:
- Anterior pituitary development: Short tales from dwarf miceCell, 1992
- Pituitary hyperplasia and gigantism in mice caused by a cholera toxin transgeneNature, 1991
- Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1Nature, 1990
- A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotypeCell, 1988
- The pituitary-specific transcription factor GHF-1 is a homeobox-containing proteinCell, 1988
- MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populationsGenomics, 1987
- Binding sites for growth hormone releasing factor on rat anterior pituitary cellsNature, 1985
- Stimulation by thyrotropin and cyclic AMP of the proliferation of quiescent canine thyroid cells cultured in a defined medium containing insulinFEBS Letters, 1983
- Immunohistological study of the anterior pituitary gland ? pars distalis and pars intermedia ? in dwarf miceCell and tissue research, 1982
- A possible role for cyclic AMP in the initiation of DNA synthesis by isoproterenol‐activated parotid gland cellsJournal of Cellular Physiology, 1980