Positive and negative regulatory elements in the late lactation protein-A gene promoter from the tammar wallaby (Macropus eugenii)

Biochimica et Biophysica Acta - Gene Structure and Expression

Volumn 1728, Issue 1-2, 2005, Pages 65-76

  Trott, Josephine F ^a,c   Adams, Timothy E ^b   Wilson, Michael ^a,d   Nicholas, Kevin R ^a,e  

^a VIC INSTITUTE OF ANIMAL SCIENCE   (Australia)

^b CSIRO   (Australia)

^c UNIVERSITY OF VERMONT   (United States)

^d GLAXOSMITHKLINE   (United Kingdom)

^e UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

Exon structure; Gene regulation; Inhibitor element; Marsupial; Milk protein; Transgenic

Indexed keywords

ALKALINE PHOSPHATASE; LATE LACTATION PROTEIN A; MILK PROTEIN; STAT5 PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; BINDING AFFINITY; CHINESE HAMSTER; CONTROLLED STUDY; DNA FLANKING REGION; DOWN REGULATION; ENZYME RELEASE; EXON; GENE CONSTRUCT; GENE CONTROL; GENE DELETION; GENE EXPRESSION REGULATION; GENE IDENTIFICATION; GENE STRUCTURE; GENOMICS; LACTATION; MACROPUS EUGENII; MARSUPIAL; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE BINDING SITE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN BINDING; REPORTER GENE; TRANSCRIPTION REGULATION; TRANSGENIC MOUSE;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS; MACROPUS EUGENII; METATHERIA; MUS MUSCULUS;

EID: 15744388935     PISSN: 01674781     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbaexp.2005.01.013     Document Type: Article

References (54)

1. C.H. Tyndale-Biscoe, and M.B. Renfree Reproductive physiology of marsupials 1987 Cambridge University Press Cambridge
2. C.H. Tyndale-Biscoe, and P.A. Janssens C.H. Tyndale-Biscoe P.A. Janssens The developing marsupial: models for biomedical research 1988 Springer-Verlag Heidelberg 1 8
3. M. Messer, and B. Green Milk carbohydrates of marsupials: II. Qualitative and quantitative changes in milk carbohydrates during lactation in the tammar wallaby (Macropus eugenii) Aust. J. Biol. Sci. 32 1979 519 531
4. B. Green Composition of milk and energetics of growth in marsupials Symp. Zool. Soc. Lond. 51 1984 369 387
5. B. Green, and J.C. Merchant The composition of marsupial milk C.H. Tyndale-Biscoe P.A. Janssens The developing marsupial: models for biomedical research 1988 Springer-Verlag Heidelberg 41 54
6. K.R. Nicholas, K. Simpson, M. Wilson, J.F. Trott, and D.C. Shaw The tammar wallaby: a model to study putative autocrine-induced changes in milk composition J. Mammary Gland Biol. Neoplasia 2 1997 299 310
7. C. Collet, R. Joseph, and K.R. Nicholas Molecular cloning and characterization of a novel marsupial milk protein gene Biochem. Biophys. Res. Commun. 164 1989 1380 1383
8. O.U. Beg, and D.C. Shaw The complete primary structure of late lactation protein from quokka (Setonix brachyurus) J. Protein. Chem. 13 1994 513 516
9. C.P. Piotte, A.K. Hunter, C.J. Marshall, and M.R. Grigor Phylogenetic analysis of three lipocalins present in the milk of Trichosurus vulpecula (Phalangridae Marsupialia) J. Mol. Evol. 46 1998 361 369
10. J.F. Trott, M.J. Wilson, R.C. Hovey, D.C. Shaw, and K.R. Nicholas Expression of novel lipocalin-like milk protein gene is developmentally- regulated during lactation in the tammar wallaby, Macropus eugenii Gene 283 2002 287 297
11. K.R. Nicholas, M. Messer, C. Elliott, F. Maher, and D.C. Shaw A novel whey protein synthesised only in late lactation by the mammary gland from the tammar (Macropus eugenii) Biochem. J. 241 1987 899 904
12. J. Demmer, S.J. Stasiuk, M.R. Grigor, K.J. Simpson, and K.R. Nicholas Differential expression of the whey acidic protein gene during lactation in the brushtail possum (Trichosurus vulpecula) Biochim. Biophys. Acta 1522 2001 187 194
13. K.R. Nicholas, and C.H. Tyndale-Biscoe Prolactin-dependent accumulation of a-lactalbumin in mammary gland explants from the pregnant tammar wallaby (Macropus eugenii) J. Endocrinol. 106 1985 337 342
14. C. Collet, R. Joseph, and K.R. Nicholas Cloning, cDNA analysis and prolactin-dependent expression of a marsupial a-lactalbumin Reprod. Fertil. Dev. 2 1990 693 701
15. C. Collet, R. Joseph, and K.R. Nicholas A marsupial β-lactoglobulin gene: characterization and prolactin-dependent expression J. Mol. Endocrinol. 6 1991 9 16
16. C. Collet, R. Joseph, and K.R. Nicholas Molecular characterization and in vitro hormonal requirements for expression of two casein genes from a marsupial J. Mol. Endocrinol. 8 1992 13 20
17. K.R. Nicholas, C.J. Wilde, P.H. Bird, K.A.K. Hendry, K. Tregenza, and B. Warner Asynchronous concurrent secretion of milk proteins in the tammar wallaby (Macropus eugenii) C.J. Wilde M. Peaker C.H. Knight Intercellular signalling in the mammary gland 1995 Plenum Press New York 153 170
18. N.E. Hynes, N. Cella, and M. Wartmann Prolactin mediated intracellular signalling in mammary epithelial cells J. Mammary Gland Biol. Neoplasia 2 1997 19 27
19. M. Schmitt-Ney, W. Doppler, R.K. Ball, and B. Groner β-Casein gene promoter activity is regulated by the hormone-mediated relief of transcriptional repression and a mammary gland-specific nuclear factor Mol. Cell. Biol. 11 1991 3745 3755
20. T.G. Burdon, J. Demmer, A.J. Clark, and C.J. Watson The mammary factor MPBF is a prolactin-induced transcriptional regulator which binds to STAT factor recognition sites FEBS Lett. 350 1994 177 182
21. J.N. Ihle STATs: signal transducers and activators of transcription Cell 84 1996 331 334
22. D.W. Lincoln, and M.B. Renfree Mammary gland growth and milk ejection in the agile wallaby, Macropus agilis, displaying concurrent asynchronous lactation J. Reprod. Fertil. 63 1981 193 203
23. K.R. Nicholas Control of milk protein synthesis in the marsupial Macropus eugenii: a model system to study prolactin-dependent development C.H. Tyndale-Biscoe P.A. Janssens The developing marsupial: models for biomedical research 1988 Springer-Verlag Heidelberg 68 85
24. L. Lesueur, M. Edery, J. Paly, P.A. Kelly, and J. Djiane Roles of extracellular and cytoplasmic domains of the prolactin receptor in signal transduction to milk protein genes Mol. Endocrinol. 7 1993 1178 1184
25. J. Djiane, N. Daniel, C. Bignon, J. Paly, M. Waters, P. Vacher, and B. Dufy Prolactin receptor and signal transduction to milk protein genes Proc. Soc. Exp. Biol. Med. 206 1994 299 303
26. H.N. Jabbour, L.A. Clarke, S. Boddy, A. Pezet, M. Edery, and P.A. Kelly Cloning, sequencing and functional analysis of a truncated cDNA encoding red deer prolactin receptor: an alternative tyrosine residue mediates β-casein promoter activation Mol. Cell. Endocrinol. 123 1996 17 26
27. L. Hennighausen The prospects for domesticating milk protein genes J. Cell. Biochem. 49 1992 325 332
28. J. Sambrook, E.F. Fritsch, and T. Maniatis Molecular cloning: a laboratory manual 2nd ed. 1989 Cold Spring Harbor Laboratory Press Cold Spring Harbor, New York
29. S.J. Triezenberg Primer extension F.M. Ausubel R. Brent R.E. Kingston D.D. Moore J.A. Smith J.G. Seidman K. Struhl Current protocols in molecular biology 1996 John Wiley & Sons, Inc. New York
30. E. Schreiber, P. Matthias, M.M. Muller, and W. Schaffner Rapid detection of octamer binding proteins with 'mini-extracts', prepared from a small number of cells Nucleic Acids Res. 17 1989 6418
31. H. Wakao, F. Gouilleux, and B. Groner Mammary gland factor (MGF) is a novel member of the cytokine regulated transcription factor gene family and confers the prolactin response EMBO J. 13 1994 2182 2191
32. J. Feng, B.A. Witthuhn, T. Matsuda, F. Kohlhuber, I.M. Kerr, and J.N. Ihle Activation of Jak2 catalytic activity requires phosphorylation of Y1007 in the kinase activation loop Mol. Cell. Biol. 17 1997 2497 2501
33. C.J. Watson, K.E. Gordon, M. Robertson, and A.J. Clark Interaction of DNA-binding proteins with a milk protein gene promoter in vitro: identification of a mammary gland-specific factor Nucleic Acids Res. 19 1991 6603 6610
34. W. Doppler, B. Groner, and R.K. Ball Prolactin and glucocorticoid hormones synergistically induce expression of transfected rat β-casein gene promoter constructs in a mammary epithelial cell line Proc. Natl. Acad. Sci. U. S. A. 86 1989 104 108
35. K.D. O'Neal, and L.-Y. Yu-Lee Differential signal transduction of the short, Nb2, and long prolactin receptors J. Biol. Chem. 269 1994 26076 26082
36. L. Sankaran A simple quantitative assay for chloramphenicol acetyltransferase by direct extraction of the labelled product into scintillation cocktail Anal. Biochem. 200 1992 180 186
37. P. Bird, K.A.K. Hendry, D. Shaw, C.J. Wilde, and K.R. Nicholas Progressive changes in milk protein gene expression and prolactin binding during lactation in the tammar wallaby (Macropus eugenii) J. Mol. Endocrinol. 13 1994 117 125
38. H.M. Seyfert, C. Pitra, L. Meyer, R.M. Brunner, T.T. Wheeler, A. Molenaar, J.Y. McCracken, J. Herrmann, H.J. Thiesen, and M. Schwerin Molecular characterization of STAT5A- and STAT5B-encoding genes reveals extended intragenic sequence homogeneity in cattle and mouse and different degrees of divergent evolution of various domains J. Mol. Evol. 50 2000 550 561
39. L. Lesueur, M. Edery, J. Paly, J. Clark, P.A. Kelly, and J. Djiane Prolactin stimulates milk protein promoter in CHO cells cotransfected with prolactin receptor cDNA Mol. Cell. Endocrinol. 71 1990 R7 R12
40. L. Lesueur, M. Edery, S. Ali, J. Paly, P.A. Kelly, and J. Djiane Comparison of long and short forms of the prolactin receptor on prolactin-induced milk protein gene transcription Proc. Natl. Acad. Sci. U. S. A. 88 1991 824 828
41. S. Ali, M. Edery, I. Pellegrini, L. Lesueur, J. Paly, J. Djiane, and P.A. Kelly The Nb2 form of prolactin receptor is able to activate a milk protein gene promoter Mol. Endocrinol. 6 1992 1242 1248
42. J. Demmer, T.G. Burdon, J. Djiane, C.J. Watson, and A.J. Clark The proximal milk protein binding factor binding site is required for the prolactin responsiveness of the sheep β-lactoglobulin promoter in Chinese hamster ovary cells Mol. Cell. Endocrinol. 107 1995 113 121
43. C.B. Whitelaw, S. Grolli, P. Accornero, G. Donofrio, E. Farini, and J. Webster Matrix attachment region regulates basal beta-lactoglobulin transgene expression Gene 244 2000 73 80
44. S. Pierre, G. Jolivet, E. Devinoy, M.C. Théron, R. Maliénou-N'Gassa, C. Puissant, and L.-M. Houdebine A distal region enhances the prolactin promoter activity of the rabbit as1-casein gene Mol. Cell. Endocrinol. 87 1992 147 156
45. S. Pierre, G. Jolivet, E. Devinoy, and L.-M. Houdebine A combination of distal and proximal regions is required for efficient prolactin regulation of transfected rabbit as1-casein chloramphenicol acetyltransferase constructs Mol. Endocrinol. 8 1994 1720 1730
46. M.I. Morasso, K.A. Mahon, and T.D. Sargent A Xenopus distal-less gene in transgenic mice: conserved regulation in distal limb epidermis and other sites of epithelial-mesenchymal interaction Proc. Natl. Acad. Sci. U. S. A. 92 1995 3968 3972
47. A.R. Buchman, W.J. Kimmerly, J. Rine, and R.D. Kornberg Two DNA-binding factors recognize specific sequences at silencers, upstream activating sequences, autonomously replicating sequences, and telomeres from Saccharomyces cerevisiae Mol. Cell. Biol. 8 1988 210 225
48. S.X. Cao, P.D. Gutman, H.P.G. Dave, and A.N. Schechter Identification of a transcriptional silencer in the 5′-flanking region of the human e-globin gene Proc. Natl. Acad. Sci. U. S. A. 86 1989 5306 5309
49. D.P. Ramji, M.H. Tadros, E.M. Hardon, and R. Cortese The transcription factor LF-A1 interacts with bipartite recognition sequence in the promoter regions of several liver-specific genes Nucleic Acids Res. 19 1991 1139 1146
50. J. Kim, M.-H. Yu, and K. Kim Repression participates in mammary tissue-specific activation of the caprine β-lactoglobulin promoter Mol. Cell. Endocrinol. 133 1997 161 168
51. L.S. Coles, P. Diamond, L. Lambrusco, J. Hunter, J. Burrows, M.A. Vadas, and G.J. Goodall A novel mechanism of repression of the vascular endothelial growth factor promoter, by single strand DNA binding cold shock domain (Y-box) proteins in normoxic fibroblasts Nucleic Acids Res. 30 2002 4845 4854
52. C. Terraz, D. Toman, M. Delauche, P. Ronco, and J. Rossert Delta Ef1 binds to a far upstream sequence of the mouse pro-alpha 1(I) collagen gene and represses its expression in osteoblasts J. Biol. Chem. 276 2001 37011 37019
53. R. Sekido, K. Murai, J. Funahashi, Y. Kamachi, A. Fujisawa-Sehara, Y. Nabeshima, and H. Kondoh The delta-crystallin enhancer-binding protein delta EF1 is a repressor of E2-box-mediated gene activation Mol. Cell. Biol. 14 1994 5692 5700
54. K.R. Sensenbaugh, and M.M. Sanders Multiple promoter elements including a novel repressor site modulate expression of the chick ovalbumin gene DNA Cell Biol. 18 1999 147 156