Zinc finger proteins RUSH in where others fear to tread

Biology of Reproduction

Volumn 58, Issue 2, 1998, Pages 285-294

  Chilton, Beverly S ^a   Hewetson, Aveline ^a  

^a TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; PROGESTERONE; PROLACTIN; PROTEIN RUSH 1ALPHA; PROTEIN RUSH 1BETA; UNCLASSIFIED DRUG; UTEROGLOBIN; ZINC FINGER PROTEIN;

ALTERNATIVE RNA SPLICING; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; BASE PAIRING; CARBOXY TERMINAL SEQUENCE; CONFERENCE PAPER; CONTROLLED STUDY; DNA FLANKING REGION; ESTRUS; GENETIC TRANSCRIPTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MULTIGENE FAMILY; NONHUMAN; OVARIECTOMY; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN SECRETION; PROTEIN SYNTHESIS; RABBIT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DNA-BINDING PROTEINS; FEMALE; HUMANS; MOLECULAR SEQUENCE DATA; PREGNANCY; RABBITS; RATS; TRANSCRIPTION FACTORS; ZINC FINGERS;

ANIMALIA; ORYCTOLAGUS CUNICULUS;

EID: 0031885185     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod58.2.285     Document Type: Conference Paper

References (98)

1. Sawadogo M, Sentenac A. RNA polymerase B (II) and general transcription factors. Annu Rev Biochem 1990; 59:711-754.
2. Buratowski S. The basics of basal transcription by RNA polymerase II. Cell 1994; 77:1-3.
3. Tjian R, Maniatis T. Transcriptional activation: a complex puzzle with few easy pieces. Cell 1994; 77:5-8.
4. Angel P, Karin M. The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation. Biochim Biophys Acta 1991; 1072: 129-157.
5. Scott MP, Tamkun JW, Hartzell III BW. The structure and function of the homeodomain. Biochim Biophys Acta 1989; 989:25-48.
6. Vedeckis WV. Nuclear receptors, transcriptional regulation and oncogenesis. Proc Soc Exp Biol Med 1991; 199:1-12.
7. Mitchell PJ, Tjian R. Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins. Science 1989; 245:371-378.
8. Krajewska WM. Regulation of transcription in eukaryotes by DNA-binding proteins. Int J Biochem 1992; 24:1885-1898.
9. Ptashne M. How transcriptional activators work. Nature 1988; 335: 683-689.
10. Courey AJ, Tjian R. Analysis of Sp1 in vivo reveals multiple transcriptional domains, including a novel glutamine-rich activation motif. Cell 1988; 55:887-898.
11. Mermod N, O'Neill EA, Kelly TJ, Tjian R. The proline-rich transcriptional activator of CTF/NF-I is distinct from the replication and DNA binding domain. Cell 1989; 58:741-753.
12. Gronemeyer H. Transcription activation by estrogen and progesterone receptors. Annu Rev Genet 1991; 25:89-123.
13. Mangelsdorf DJ, Thummel C, Beato M, Herrlich P, Schutz G, Umesono K, Blumberg B, Kastner P, Mark M, Chambon P, Evans RM. The nuclear receptor superfamily: the second decade. Cell 1995; 83: 835-839.
14. Horwitz KB, Jackson TA, Bain DL, Richer JK, Takimoto GS, Tung L. Nuclear receptor coactivators and corepressors. Mol Endocrinol 1996; 10:1167-1177.
15. Wilson CJ, Chao DM, Imbalzano AN, Schnitzler GR, Kingston RE, Young RA. RNA polymerase II holoenzyme contains SWI/SNF regulators involved in chromatin remodeling. Cell 1996; 84:235-244.
16. Yoshinaga SK, Peterson CL, Herskowitz I, Yamamoto KR. Roles of SWI1, SWI2, and SWI3 proteins for transcriptional enhancement by steroid receptors. Science 1992; 258:1598-1604.
17. Winston F, Carlson M. Yeast SNF/SWI transcriptional activators and the SPT/SIN chromatin connection. Trends Genet 1992; 8:387-391.
18. Carlson M, Laurent BC. The SNF/SWI family of global transcriptional activators. Curr Opin Cell Biol 1994; 6:396-402.
19. Muchardt C, Yaniv M. A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor. EMBO J 1993; 12: 4279-4290.
20. Khavari PA, Peterson CL, Tamkun JW, Mendel DB, Crabtree GR. BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription. Nature 1993; 366: 170-174.
21. Le Douarin B, Zechel C, Garnier J-M, Lutz Y, Tora L, Pierrat B, Heery D, Gronemeyer H, Chambon P, Losson R. The N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18. EMBO J 1995; 14:2020-2033.
22. Freemont PS, Hanson IM, Trowsdale J. A novel cysteine-rich sequence motif. Cell 1991; 64:483-484.
23. Freemont PS. The RING finger. Ann NY Acad Sci 1993; 684:174-192.
24. Saurin AJ, Borden KLB, Boddy MN, Freemont PS. Does this have a familiar RING? Trends Biochem Sci 1996; 21:208-214.
25. 4 domain by H-nuclear magnetic resonance spectroscopy. J Mol Biol 1994; 237:201-211.
26. Arthur A, Daniel JC Jr. Progesterone regulation of blastokinin production and maintenance of rabbit blastocysts transferred into uteri of castrate recipients. J Fertil Steril 1972; 23:115-122.
27. Roberts RM, Bazer FW. The properties, function and hormonal control of synthesis of uteroferrin, the purple protein of the pig uterus. In: Beato M (ed.), Steroid Induced Uterine Proteins. Elsevier: Developments in Endocrinology; 1980: 8:133-152.
28. Beato M, Chalepakis G, Schauer M, Slater EP. DNA regulatory elements for steroid hormones. J Steroid Biochem 1989; 32:737-748.
29. Popp RA, Foresman KR, Wise LD, Daniel JC Jr. Amino-acid sequence of a progesterone-binding protein. Proc Natl Acad Sci USA 1978; 75:5516-5519.
30. Mukherjee AB, Ulane RE, Agrawal AK. Role of uteroglobin and transglutaminase in masking the antigenicity of implanting rabbit embryos. J Reprod Immunol 1982; 2:135-141.
31. Miele L, Cordella-Miele E, Facchiano A, Mukherjee AB. Novel antiinflammatory peptides from the region of the highest similarity between uteroglobin and lipocortin I. Nature 1988; 355:726-730.
32. Krishnan RS, Daniel JC Jr. "Blastokinin": inducer and regulator of blastocyst development in the rabbit uterus. Science 1967; 158:490-492.
33. Beier HM. Uteroglobin: a hormone-sensitive endometrial protein involved in blastocyst development. Biochim Biophys Acta 1968; 160: 289-291.
34. Peri A, Cowan BD, Bhartiya D, Miele L, Nieman LK, Nwaeze IO, Mukherjee AB. Expression of Clara cell 10-kDa gene in the human endometrium and its relationship to ovarian menstrual cycle. DNA Cell Biol 1994; 13:495-503.
35. Kundu GC, Mantile G, Miele L, Cordella-Mielle E, Mukherjee AB. Recombinant human uteroglobin suppresses cellular invasiveness via a novel class of high affinity cell surface binding site. Proc Natl Acad Sci USA 1996; 93:2915-2919.
36. Cato ACB, Beato M. The hormone regulation of uteroglobin gene expression. Anticancer Res 1985; 5:65-72.
37. 2 inhibitor. Endocr Rev 1987; 8:474-490.
38. Chandra T, Bullock DW, Woo SLC. Hormonally regulated mammalian gene expression: steady-state level and nucleotide sequence of rabbit uteroglobin mRNA. DNA 1981; 1:19-26.
39. Snead R, Day L, Chandra T, Mace M, Bullock DW, Woo SLC. Mosaic structure and mRNA precursors of uteroglobin, a hormone-regulated mammalian gene. J Biol Chem 1981; 256:11911-11916.
40. Shen X-Z, Tsai MJ, Bullock DW, Woo SLC. Hormonal regulation of rabbit uteroglobin gene transcription. Endocrinology 1983; 112:871-876.
41. Bullock DW. In vitro translation of messenger RNA for a uteroglobin-like protein from rabbit lung. Biol Reprod 1977; 17:104-107.
42. Miele L, Cordella-Miele E, Mantile G, Peri A, Mukherjee AB. Uteroglobin and uteroglobin-like proteins: the uteroglobin family of proteins. J Endocrinol Invest 1994; 17:679-692.
43. Kay E, Feigelson M. An estrogen modulated protein in rabbit oviductal fluid. Biochim Biophys Acta 1972; 271:436-441.
44. Urzua MA, Stambaugh R, Flickinger G, Mastroianni L. Uterine and oviduct protein patterns in the rabbit before and after ovulation. Fertil Steril 1970; 21:860-865.
45. Bullock DW, Willen GF. Regulation of a specific uterine protein by estrogen and progesterone in ovariectomized rabbits. Proc Soc Exp Biol Med 1974; 146:294-298.
46. Rahman SS, Billiar RB, Little B. Induction of uteroglobin in rabbits by progesterone, estradiol-17β and ACTH. Biol Reprod 1975; 12: 305-314.
47. Fridlanski F, Milgrom E. Interaction of uteroglobin with progesterone, 5α pregnane-3,20-dione and estrogens. Endocrinology 1976; 99: 1244-1251.
48. Daniel JC Jr. Factors influencing uteroglobin synthesis. In: Beato M (ed.), Steroid Induced Uterine Proteins. Amsterdam: Elsevier/North Holland Biomedical Press; 1980: 87-103.
49. Martinet L, Allais C, Allain D. The role of prolactin and LH in luteal function and blastocyst growth in mink (Mustela vison), J Reprod Fertil Suppl 1981; 29:119-130.
50. Murphy BD, Concannon PW, Travis HF, Hansel W. Prolactin: the hypophyseal factor that terminates embryonic diapause in mink. Biol Reprod 1981; 25:487-491.
51. Daniel JC Jr, Jetton AE, Chilton BS. Prolactin as a factor in the uterine response to progesterone in rabbits. J Reprod Fertil 1984; 72:443-452.
52. Chilton BS, Daniel JC Jr. Influence of prolactin on DNA synthesis and glandular differentiation in rabbit uterine endometrium. In: MacLeod RM, Turner MO, Scapagnini U (eds.), Prolactin Basic and Clinical Correlates. Pavoda, Italy: Liviana Press, Fidia Research Series; 1985: 1:351-359.
53. Chilton BS, Daniel JC Jr. Differences in the rabbit uterine response to progesterone as influenced by growth hormone or prolactin. J Reprod Fertil 1987; 79:581-587.
54. Davies J, Hesseldahl H. Comparative embryology of mammalian blastocysts. In: Blandau RJ (ed.), The Biology of the Blastocyst. London, UK: The University of Chicago Press Ltd.; 1971: 27-48.
55. Goffin V, Shiverick KT, Kelly PA, Martial JA. Sequence-function relationships within the expanding family of prolactin, growth hormone, placental lactogen, and related proteins in mammals. Endocr Rev 1996; 17:385-410.
56. Daniel JC Jr, Juneja SC, Taylor SP, Lonergan PB, Sullivan PK, Chilton BS. Variability in the response of the rabbit uterus to progesterone as influenced by prolactin. J Reprod Fertil 1988; 84:13-21.
57. Chilton BS, Mani SK, Bullock DW. Servomechanism of prolactin and progesterone in regulating uterine gene expression. Mol Endocrinol 1988; 2:1169-1175.
58. Randall GW, Daniel JC Jr, Chilton BS. Prolactin enhances uteroglobin gene expression by uteri of immature rabbits. J Reprod Fertil 1991; 91:249-257.
59. Daniel JC Jr, Juneja SC. Amplification of uteroglobin secretion by alternating prolactin-progesterone administration. J Endocrinol 1989; 122:R5-R6.
60. Muccioli G, Lando D, Bellussi G, Di Carlo R. Physiological and pharmacological variations in rabbit prolactin plasma levels. Life Sci 1983; 32:703-710.
61. Kao LWL, Bullock DW. Rates of uteroglobin synthesis by endometrial explants from different days of early pregnancy in the rabbit. Biol Reprod 1981; 25:820-824.
62. Jantzen K, Fritton KP, Igo-Kemenes T, Espel E, Janich S, Cato CB, Mugele K, Beato M. Partial overlapping of binding sequences for steroid hormone receptors and DNase I hypersensitive sites in the rabbit uteroglobin gene region. Nucleic Acid Res 1987; 15:4535-4552.
63. Slater EP, Redeuihl G, Theis K, Suske G, Beato M. The uteroglobin promoter contains a noncanonical estrogen response element. Mol Endocrinol 1990; 4:604-610.
64. Dennig J, Hagen G, Beato M, Suske G. Members of the Sp transcription factor family control transcription from the uteroglobin promoter. J Biol Chem 1995; 270:12737-12744.
65. Suske G, Lorenz W, Klug J, Gazdar AF, Beato M. Elements in the rabbit uteroglobin promoter mediating its transcription in epithelial cells from the endometrium and lung. Gene Expression 1992; 2:339-353.
66. Hagen G, Muller S, Beato M, Suske G. Cloning by recognition site screening of two novel GT box binding proteins: a family of Sp1 related genes. Nucleic Acids Res 1992; 20:5519-5525.
67. Klug J, Knapp S, Castro I, Beato M. Two distinct factors bind to the rabbit uteroglobin TATA-box region and are required for efficient transcription. Mol Cell Biol 1994; 14:6208-6218.
68. Wolf M, Klug J, Hackenberg R, Gessler M, Grzeschik K-H, Beato M, Suske G. Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines. Hum Mol Genet 1992; 1:371-378.
69. DeMayo FJ, Damak S, Hansen TN, Bullock DW. Expression and regulation of the rabbit uteroglobin gene in transgenic mice. Mol Endocrinol 1991; 5:311-318.
70. Rider V, Bullock DW. Progesterone-dependent binding of a transacting factor to the uteroglobin promoter. Biochem Biophys Res Commun 1988; 156:1368-1375.
71. Rider V, Peterson CJ. Activation of uteroglobin gene expression by progesterone is modulated by uterine-specific promoter-binding proteins. Mol Endocrinol 1991; 5:911-920.
72. Kleis-SanFrancisco S, Hewetson A, Chilton BS. Prolactin augments progesterone-dependent uteroglobin gene expression by modulating promoter-binding proteins. Mol Endocrinol 1993; 7:214-223.
73. Hayward-Lester A, Hewetson A, Beale EG, Oefner PJ, Doris PA, Chilton BS. Cloning, characterization and steroid-dependent posttranscriptional processing of RUSH-1α & β, two uteroglobin promoter binding proteins. Mol Endocrinol 1996; 10:1335-1349.
74. Hayward-Lester A, Oefner PJ, Sabatini S, Doris PA. Accurate and absolute quantitative measurement of gene expression by single-tube RT-PCR and HPLC. Genome Res 1995; 5:494-499.
75. Hayward-Lester A, Oefner PJ, Doris PA. Rapid quantification of gene expression by competitive RT-PCR and ion-pair reversed-phase HPLC. Biotechniques 1996; 20:250-257.
76. Watson CJ, Burdon TG. Prolactin signal transduction mechanisms in the mammary gland: the role of the Jak/Stat pathway. Rev Reprod 1996; 1:1-5.
77. Clevenger CV, Altmann SW, Prystowsky MB. Requirement of nuclear prolactin for interleukin-2-stimulated proliferation of T lymphocytes. Science 1991; 253:77-79.
78. Clevenger CV, Medaglia MV. The protein tyrosine kinase p59fyn is associated with prolactin receptor and is activated by prolactin stimulation of T-lymphocytes. Mol Endocrinol 1994; 8:674-681.
79. Sharp PA. Split genes and RNA splicing. Cell 1994; 77:805-815.
80. Smith CWJ, Patton JG, Nadal-Ginard B. Alternative splicing in the control of gene expression. Annu Rev Genet 1989; 23:527-577.
81. McKeown M. Alternative mRNA splicing. Annu Rev Cell Biol 1992; 8:133-155.
82. Foulkes NS, Sassone-Corsi P. More is better: activators and repressors from the same gene. Cell 1992; 68:411-414.
83. Rio DC. Splicing of pre-mRNA: mechanism, regulation and role in development. Curr Opin Genet Dev 1993; 3:574-584.
84. Jans DA, Hubner S. Regulation of protein transport to the nucleus: central role of phosphorylation. Physiol Rev 1996; 76:651-685.
85. Kuiper GG, Brinkmann AO. Steroid hormone receptor phosphorylation: is there a physiological role? Mol Cell Endocrinol 1994; 100: 103-107.
86. Karin M. Signal transduction from the cell surface to the nucleus through the phosphorylation of transcription factors. Curr Opin Cell Biol 1994; 6:415-424.
87. Robinson CA, Hayward-Lester A, Hewetson A, Oefner PJ, Doris PJ, Chilton BS. Quantification of alternatively spliced RUSH mRNA isoforms by QRT-PCR and IP-RP-HPLC analysis: a new approach to measuring regulated splicing efficiency. Gene 1997; 198:1-4.
88. McKeown M. Regulation of alternative splicing. In: Setlow JK (ed.), Genetic Engineering, Principles and Methods. New York: Plenum; 1990: 12:139-181.
89. Sheridan PL, Schorpp M, Voz ML, Jones KA. Cloning of an SNF2/ SWI2-related protein that binds specifically to the SPH motifs of the SV40 enhancer and to the HIV-I promoter. J Biol Chem 1995; 270: 4574-4587.
90. Li WI, Chen CL, Chou JY. Characterization of a temperature-sensitive β-endorphin-secreting transformed endometrial cell line. Endocrinology 1989; 125:2862-2867.
91. Fliss AE, Michel FJ, Chen C-L, Hofig A, Bazer FW, Chou JY, Simmen RCM. Regulation of the uteroferrin gene promoter in endometrial cells: interactions among estrogen, progesterone, and prolactin. Endocrinology 1991; 129:697-704.
92. Mukherjee AB, Murty LC, Chou JY. Differentiation and uteroglobin gene expression by novel rabbit endometrial cell lines. Mol Cell Endocrinol 1993; 94:R15-R22.
93. Misseyanni A, Klug J, Suske G, Beato M. Novel upstream elements and the TATA-box region mediate preferential transcription from the uteroglobin promoter in endometrial cells. Nucleic Acids Res 1991; 19:2849-2859.
94. Fuchs A-R, Cubile L, Dawood MY. Effects of mating on levels of oxytocin and prolactin in the plasma of male and female rabbits. J Endocrinol 1981; 90:245-253.
95. McNeilly AS, Friesen HG. Prolactin during pregnancy and lactation in the rabbit. Endocrinology 1978; 102:1548-1554.
96. Durand P, Djiane J. Lactogenic activity in the serum of rabbits during pregnancy and early lactation. J Endocrinol 1977; 75:33-42.
97. McNeilly AS, Friesen HG. Heterologous radioimmunoassay for rabbit prolactin. Endocrinology 1978; 102:1539-1547.
98. Seidel HM, Milocco LH, Lamb P, Darnell JE Jr, Stein RB, Rosen J. Spacing of palindromic half sites as a determinant of selective STAT (signal transducers and activators of transcription) DNA binding and transcriptional activity. Proc Natl Acad Sci USA 1995; 92:3041-3045.