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Research Papers
Eukaryotic Regulatory Biology Program, University of California, San Diego, La Jolla 92093.
Abstract
The anterior pituitary gland provides a model for investigating the molecular basis for the appearance of phenotypically distinct cell types within an organ, a central question in development. The rat prolactin and growth hormone genes are expressed selectively in distinct cell types (lactotrophs and somatotrophs, respectively) of the anterior pituitary gland, reflecting differential mechanisms of gene activation or restriction, as a result of the interactions of multiple factors binding to these genes. We find that when the pituitary-specific 33-kD transcription factor Pit-1, expressed normally in both lactotrophs and somatotrophs, is expressed in either the heterologous HeLa cell line or in bacteria, it binds to and activates transcription from both growth hormone and prolactin promoters in vitro at levels even 10-fold lower than those normally present in pituitary cells. This suggests that a single factor, Pit-1, may be capable of activating the expression of two genes that define different anterior pituitary cell phenotypes. Because a putative lactotroph cell line (235-1) that does not express the growth hormone gene, but only the prolactin gene, appears to contain high levels of functional Pit-1, a mechanism selectively preventing growth hormone gene expression may, in part, account for the lactotroph phenotype.
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S M Lipkin, A M Naar, K A Kalla, R A Sack, and M G Rosenfeld Identification of a novel zinc finger protein binding a conserved element critical for Pit-1-dependent growth hormone gene expression. Genes & Dev., September 1, 1993; 7(9): 1674 - 1687. [Abstract] [PDF] |
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S J Rhodes, R Chen, G E DiMattia, K M Scully, K A Kalla, S C Lin, V C Yu, and M G Rosenfeld A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the pit-1 gene. Genes & Dev., June 1, 1993; 7(6): 913 - 932. [Abstract] [PDF] |
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D Lew, H Brady, K Klausing, K Yaginuma, L E Theill, C Stauber, M Karin, and P L Mellon GHF-1-promoter-targeted immortalization of a somatotropic progenitor cell results in dwarfism in transgenic mice. Genes & Dev., April 1, 1993; 7(4): 683 - 693. [Abstract] [PDF] |
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S. Radovick, M. Nations, Y. Du, L. A. Berg, B. D. Weintraub, and F. E. Wondisford A Mutation in the POU-Homeodomain of Pit-1 Responsible for Combined Pituitary Hormone Deficiency Science, August 21, 1992; 257(5073): 1115 - 1118. [Abstract] [PDF] |
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R. W. Pfaffle, G. E. DiMattia, J. S. Parks, M. R. Brown, J. M. Wit, M. Jansen, H. Van der Nat, J. L. Van den Brande, M. G. Rosenfeld, and H. A. Ingraham Mutation of the POU-Specific Domain of Pit-1 and Hypopituitarism Without Pituitary Hypoplasia Science, August 21, 1992; 257(5073): 1118 - 1121. [Abstract] [PDF] |
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D W Drolet, K M Scully, D M Simmons, M Wegner, K T Chu, L W Swanson, and M G Rosenfeld TEF, a transcription factor expressed specifically in the anterior pituitary during embryogenesis, defines a new class of leucine zipper proteins. Genes & Dev., October 1, 1991; 5(10): 1739 - 1753. [Abstract] [PDF] |
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M. Kapiloff, Y Farkash, M Wegner, and M. Rosenfeld Variable effects of phosphorylation of Pit-1 dictated by the DNA response elements Science, August 16, 1991; 253(5021): 786 - 789. [Abstract] [PDF] |
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A D Reith and A Bernstein Molecular basis of mouse developmental mutants. Genes & Dev., July 1, 1991; 5(7): 1115 - 1123. [PDF] |
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J W Voss, L Wilson, and M G Rosenfeld POU-domain proteins Pit-1 and Oct-1 interact to form a heteromeric complex and can cooperate to induce expression of the prolactin promoter. Genes & Dev., July 1, 1991; 5(7): 1309 - 1320. [Abstract] [PDF] |
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M G Rosenfeld POU-domain transcription factors: pou-er-ful developmental regulators. Genes & Dev., June 1, 1991; 5(6): 897 - 907. [PDF] |
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A Travis, A Amsterdam, C Belanger, and R Grosschedl LEF-1, a gene encoding a lymphoid-specific protein with an HMG domain, regulates T-cell receptor alpha enhancer function [corrected] Genes & Dev., May 1, 1991; 5(5): 880 - 894. [Abstract] [PDF] |
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D M Simmons, J W Voss, H A Ingraham, J M Holloway, R S Broide, M G Rosenfeld, and L W Swanson Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors. Genes & Dev., May 1, 1990; 4(5): 695 - 711. [Abstract] [PDF] |
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C K Tuggle, J Zakany, L Cianetti, C Peschle, and M C Nguyen-Huu Region-specific enhancers near two mammalian homeo box genes define adjacent rostrocaudal domains in the central nervous system. Genes & Dev., February 1, 1990; 4(2): 180 - 189. [Abstract] [PDF] |
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H P Elsholtz, V R Albert, M N Treacy, and M G Rosenfeld A two-base change in a POU factor-binding site switches pituitary-specific to lymphoid-specific gene expression. Genes & Dev., January 1, 1990; 4(1): 43 - 51. [Abstract] [PDF] |
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E B Crenshaw, K Kalla, D M Simmons, L W Swanson, and M G Rosenfeld Cell-specific expression of the prolactin gene in transgenic mice is controlled by synergistic interactions between promoter and enhancer elements. Genes & Dev., July 1, 1989; 3(7): 959 - 972. [Abstract] [PDF] |
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K. K. Jacob and F. M. Stanley Elk-1, C/EBPalpha , and Pit-1 Confer an Insulin-responsive Phenotype on Prolactin Promoter Expression in Chinese Hamster Ovary Cells and Define the Factors Required for Insulin-increased Transcription J. Biol. Chem., June 29, 2001; 276(27): 24931 - 24936. [Abstract] [Full Text] [PDF] |
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