Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors.

Development of the anterior pituitary gland involves proliferation and differentiation of ectodermal cells in Rathke's pouch to generate five distinct cell types that are defined by the trophic hormones they produce. A detailed ontogenetic analysis of specific gene expression has revealed novel aspects of organogenesis in this model system. The expression of transcripts encoding the alpha-subunit common to three pituitary glycoprotein hormones in the single layer of somatic ectoderm on embryonic day 11 established that primordial pituitary cell commitment occurs prior to formation of a definitive Rathke's pouch. Activation of Pit-1 gene expression occurs as an organ-specific event, with Pit-1 transcripts initially detected in anterior pituitary cells on embryonic day 15. Levels of Pit-1 protein closely parallel those of Pit-1 transcripts without a significant lag. Unexpectedly, Pit-1 transcripts remain highly expressed in all five cell types of the mature pituitary gland, but the Pit-1 protein is detected in only three cell types--lactotrophs, somatotrophs, and thyrotrophs and not in gonadotrophs or corticotrophs. The presence of Pit-1 protein in thyrotrophs suggests that combinatorial actions of specific activating and restricting factors act to confine prolactin and growth hormone gene expression to lactotrophs and somatotrophs, respectively. A linkage between the initial appearance of Pit-1 protein and the surprising coactivation of prolactin and growth hormone gene expression is consistent with the model that Pit-1 is responsible for the initial transcriptional activation of both genes. The estrogen receptor, which has been reported to be activated in a stereotypic fashion subsequent to the appearance of Pit-1, appears to be capable, in part, of mediating the progressive increase in prolactin gene expression characteristic of the mature lactotroph phenotype. This is a consequence of synergistic transcriptional effects with Pit-1, on the basis of binding of the estrogen receptor to a response element in the prolactin gene distal enhancer. These data imply that both transcriptional and post-transcriptional regulation of Pit-1 gene expression and combinatorial actions with other classes of transcription factors activated in distinct temporal patterns, are required for the mature physiological patterns of gene expression that define distinct cell types within the anterior pituitary gland.

[1]  M. Treacy,et al.  Characterisation of tissue-specific trans-acting factor binding to a proximal element in the rat growth hormone gene promoter. , 1990, European journal of biochemistry.

[2]  S. R. Fox,et al.  The homeodomain protein, Pit-1/GHF-1, is capable of binding to and activating cell-specific elements of both the growth hormone and prolactin gene promoters. , 1990, Molecular endocrinology.

[3]  R. Rickles,et al.  Regulated polyadenylation controls mRNA translation during meiotic maturation of mouse oocytes. , 1989, Genes & development.

[4]  C. Glass,et al.  Positive and negative regulation of gene transcription by a retinoic acid-thyroid hormone receptor heterodimer , 1989, Cell.

[5]  L. Swanson,et al.  A complete protocol for in situ hybridization of messenger RNAs in brain and other tissues with radi , 1989 .

[6]  J. Roberts,et al.  Analysis of proopiomelanocortin gene expression during prenatal development of the rat pituitary gland. , 1989, Molecular endocrinology.

[7]  M. Hentze,et al.  The iron-responsive element binding protein: a method for the affinity purification of a regulatory RNA-binding protein. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[8]  M. Rebagliati An RNA recognition motif in the bicoid protein , 1989, Cell.

[9]  Barbara Neupert,et al.  A specific mRNA binding factor regulates the iron-dependent stability of cytoplasmic transferrin receptor mRNA , 1989, Cell.

[10]  L. Swanson,et al.  Expression of a large family of POU-domain regulatory genes in mammalian brain development , 1989, Nature.

[11]  K. Westlund,et al.  Characterization of anterior pituitary target cells for arginine vasopressin: including cells that store adrenocorticotropin, thyrotropin-beta, and both hormones. , 1989, Endocrinology.

[12]  M. Rosenfeld,et al.  A pituitary POU domain protein, Pit-1, activates both growth hormone and prolactin promoters transcriptionally. , 1989, Genes & development.

[13]  P. Sawchenko,et al.  Transgenic mice with inducible dwarfism , 1989, Nature.

[14]  M. Karin,et al.  Purification of growth hormone-specific transcription factor GHF-1 containing homeobox. , 1989, Science.

[15]  Larry W. Swanson,et al.  Combination of in Situ Hybridization with Immunohistochemistry and Retrograde Tract-Tracing , 1989 .

[16]  R. Roeder,et al.  A human lymphoid- specific transcription factor that activates immunoglobulin genes is a homoeobox protein , 1988, Nature.

[17]  W. Schaffner,et al.  A cloned octamer transcription factor stimulates transcription from lymphoid–specific promoters in non–B cells , 1988, Nature.

[18]  W. Herr,et al.  The ubiquitous octamer-binding protein Oct-1 contains a POU domain with a homeo box subdomain. , 1988, Genes & development.

[19]  P. Sharp,et al.  The B-cell-specific Oct-2 protein contains POU box- and homeo box-type domains. , 1988, Genes & development.

[20]  G. Ruvkun,et al.  The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products. , 1988, Genes & development.

[21]  M. Rosenfeld,et al.  A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype , 1988, Cell.

[22]  T. Deerinck,et al.  The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein , 1988, Cell.

[23]  A. Sater,et al.  Features of embryonic induction. , 1988, Development.

[24]  L. Staudt,et al.  A human protein specific for the immunoglobulin octamer DNA motif contains a functional homeobox domain , 1988, Cell.

[25]  C. Glass,et al.  The thyroid hormone receptor binds with opposite transcriptional effects to a common sequence motif in thyroid hormone and estrogen response elements , 1988, Cell.

[26]  L. Swanson,et al.  Identification of rat growth hormone genomic sequences targeting pituitary expression in transgenic mice. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[27]  J. Darnell,et al.  A liver-specific DNA-binding protein recognizes multiple nucleotide sites in regulatory regions of transthyretin, alpha 1-antitrypsin, albumin, and simian virus 40 genes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[28]  H. Munro,et al.  Cytoplasmic protein binds in vitro to a highly conserved sequence in the 5' untranslated region of ferritin heavy- and light-subunit mRNAs. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[29]  R. Palmiter,et al.  Dwarf mice produced by genetic ablation of growth hormone-expressing cells. , 1988, Genes & development.

[30]  M. Rosenfeld,et al.  Activation of cell-specific expression of rat growth hormone and prolactin genes by a common transcription factor. , 1988, Science.

[31]  M. Rosenfeld,et al.  Steroid receptor-mediated inhibition of rat prolactin gene expression does not require the receptor DNA-binding domain , 1988, Cell.

[32]  P. Sharp,et al.  Molecular cloning of an enhancer binding protein:Isolation by screening of an expression library with a recognition site DNA , 1988, Cell.

[33]  R. Evans,et al.  A single domain of the estrogen receptor confers deoxyribonucleic acid binding and transcriptional activation of the rat prolactin gene. , 1988, Molecular endocrinology.

[34]  Sean B. Carroll,et al.  The segmentation and homeotic gene network in early Drosophila development , 1987, Cell.

[35]  R. Maurer,et al.  Identification of an estrogen-responsive element from the 5'-flanking region of the rat prolactin gene , 1987, Molecular and cellular biology.

[36]  G. Crabtree,et al.  Interaction of a liver-specific nuclear factor with the fibrinogen and alpha 1-antitrypsin promoters. , 1987, Science.

[37]  R. Maurer Molecular cloning and nucleotide sequence analysis of complementary deoxyribonucleic acid for the beta-subunit of rat follicle stimulating hormone. , 1987, Molecular endocrinology.

[38]  Z. D. Sharp,et al.  Reconstitution of cell-type-specific transcription of the rat prolactin gene in vitro , 1987, Molecular and cellular biology.

[39]  I. Herskowitz Functional inactivation of genes by dominant negative mutations , 1987, Nature.

[40]  E Seifert,et al.  Analysis of Krüppel protein distribution during early Drosophila development reveals posttranscriptional regulation , 1987, Cell.

[41]  R. Hammer,et al.  The rat elastase I regulatory element is an enhancer that directs correct cell specificity and developmental onset of expression in transgenic mice , 1987, Molecular and cellular biology.

[42]  S. Loukin,et al.  Selective transcription and DNase I protection of the rat prolactin gene by GH3 pituitary cell-free extracts. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[43]  M. Karin,et al.  A pituitary-specific trans-acting factor can stimulate transcription from the growth hormone promoter in extracts of nonexpressing cells , 1987, Cell.

[44]  T. Lufkin,et al.  Identification by cell fusion of gene sequences that interact with positive trans-acting factors. , 1987, Science.

[45]  H. Samuels,et al.  Cell- and sequence-specific binding of nuclear proteins to 5'-flanking DNA of the rat growth hormone gene. , 1987, The Journal of biological chemistry.

[46]  J. Baxter,et al.  Interaction of a tissue-specific factor with an essential rat growth hormone gene promoter element , 1987, Molecular and cellular biology.

[47]  K. Wood,et al.  Firefly luciferase gene: structure and expression in mammalian cells , 1987, Molecular and cellular biology.

[48]  R. Krumlauf,et al.  Diversity of alpha-fetoprotein gene expression in mice is generated by a combination of separate enhancer elements. , 1987, Science.

[49]  R. Evans,et al.  Two different cis-active elements transfer the transcriptional effects of both EGF and phorbol esters. , 1986, Science.

[50]  G. Struhl,et al.  A molecular gradient in early Drosophila embryos and its role in specifying the body pattern , 1986, Nature.

[51]  P. Sharp,et al.  A lymphoid-specific protein binding to the octamer motif of immunoglobulin genes , 1986, Nature.

[52]  R. Evans,et al.  Discrete cis-active genomic sequences dictate the pituitary cell type-specific expression of rat prolactin and growth hormone genes , 1986, Nature.

[53]  F. Studier,et al.  Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes. , 1986, Journal of molecular biology.

[54]  M. Ptashne A Genetic Switch , 1986 .

[55]  W. Gehring,et al.  Isolation of caudal, a Drosophila homeo box‐containing gene with maternal expression, whose transcripts form a concentration gradient at the pre‐blastoderm stage , 1985, The EMBO journal.

[56]  N. L. Le Douarin,et al.  Mapping of the early neural primordium in quail-chick chimeras. I. Developmental relationships between placodes, facial ectoderm, and prosencephalon. , 1985, Developmental biology.

[57]  J. Hoeffler,et al.  Ontogeny of prolactin cells in neonatal rats: initial prolactin secretors also release growth hormone. , 1985, Endocrinology.

[58]  G. Rubin,et al.  Human DNA sequences homologous to a protein coding region conserved between homeotic genes of Drosophila , 1984, Cell.

[59]  M. Tepper,et al.  Evidence for Only One β-Luteinizing Hormone and No β-Chorionic Gonadotropin Gene in the Rat* , 1984 .

[60]  H. Horvitz,et al.  The genetic control of cell lineage during nematode development. , 1984, Annual review of genetics.

[61]  W. Rutter,et al.  Cell-specific expression controlled by the 5′-flanking region of insulin and chymotrypsin genes , 1983, Nature.

[62]  J. H. Clark,et al.  Gene Regulation by Steroid Hormones II , 1983, Springer New York.

[63]  Y. Tsuruo,et al.  Ontogenesis of hypothalamic immunoreactive ACTH cells in vivo and in vitro: role of Rathke's pouch. , 1983, Developmental Biology.

[64]  J. Roberts,et al.  Regulation of the pro-opiomelanocortin mRNA levels in rat pituitary by dopaminergic compounds. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[65]  I. Kourides,et al.  Cloning of cDNA encoding the pre-beta subunit of mouse thyrotropin. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[66]  J. Vaughan,et al.  [38] Assay of corticotropin releasing factor , 1983 .

[67]  N. Alessi,et al.  Ontogeny of opioid and related peptides in the rat cns and pituitary: an immunocytochemical study. , 1983, Life sciences.

[68]  J. Habener,et al.  alpha Subunit of rat pituitary glycoprotein hormones. Primary structure of the precursor determined from the nucleotide sequence of cloned cDNAs. , 1982, The Journal of biological chemistry.

[69]  M. Dubois,et al.  Comparative study in vivo and in vitro of the differentiation of immunoreactive corticotropic cells in fetal rat anterior pituitary. , 1982, Neuroendocrinology.

[70]  J. Rutledge,et al.  Ontogeny of growth hormone and prolactin gene expression in mice. , 1982, Endocrinology.

[71]  D. Gash,et al.  Comparison of gonadotroph, thyrotroph and mammotroph development in situ, in transplants and in organ culture. , 1982, Neuroendocrinology.

[72]  S. Daikoku,et al.  Effect of the basal diencephalon on the development of Rathke's pouch in rats: a study in combined organ cultures. , 1982, Developmental biology.

[73]  P. Nakane,et al.  Ontogenesis of adrenocorticotropin-related peptide determinants in the hypothalamus and pituitary gland of the rat. , 1982, Endocrinology.

[74]  L. Swanson,et al.  The Journal of Histochemistry and Cytochemistry Some Fluorescent Counterstains for Neuroanatomical Studies' , 2022 .

[75]  H. Kronenberg,et al.  Nucleotide sequence of the mRNA encoding the pre-alpha-subunit of mouse thyrotropin. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[76]  H. Kawano,et al.  Topographical appearance of adenohypophysial cells with special reference to the development of the portal system. , 1981, Archivum histologicum Japonicum = Nihon soshikigaku kiroku.

[77]  J. Donelson,et al.  Structure of the rat prolactin gene. , 1980, The Journal of biological chemistry.

[78]  C. Oliver,et al.  Developmental changes in brain TRH and in plasma and pituitary TSH and prolactin levels in the rat. , 1980, Biology of the neonate.

[79]  S. Daikoku,et al.  An immunohistochemical study on the cytogenesis of adenohypophysial cells in fetal rats. , 1979, Developmental biology.

[80]  R. L. Holmes,et al.  Cyto-differentiation and portal vascular development in the mouse adenohypophysis. , 1976, Journal of anatomy.

[81]  E. Southern Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.

[82]  J. Schwind The development of the hypophysis cerebri of the albino rat , 1928 .

[83]  H. Adelmann The development of the neural folds and cranial ganglia of the rat , 1925 .