Identification of mRNAs that are up-regulated after fertilization in the murine zygote by suppression subtractive hybridization

Biochemical and Biophysical Research Communications

Volumn 304, Issue 1, 2003, Pages 60-66

  Yao, Yuan Qing ^a,b   Xu, Jia Sen ^a   Lee, Will M ^a   Yeung, William S B ^a   Lee, Kai Fai ^a  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Mouse embryos; Oocyte; Preimplantation; Suppression subtractive hybridization; Zygotic gene activation

Indexed keywords

MESSENGER RNA; PROTEIN BP75; PROTEIN DERIVATIVE; PROTEOGLYCAN CORE PROTEIN; RADIXIN; SERGLYCIN; SPINDLIN; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; CELL DIVISION; CONTROLLED STUDY; DATA BASE; DNA SEQUENCE; DOT HYBRIDIZATION; EMBRYO; FEMALE; FERTILIZATION; GENE; GENE ACTIVATION; GENE EXPRESSION; GENE FUNCTION; GENE ISOLATION; GENOME; HYBRIDIZATION; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PITUITARY TUMOR TRANSFORMING GENE; PRIORITY JOURNAL; PROTEIN ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SUPPRESSION SUBTRACTIVE HYBRIDIZATION; UPREGULATION; ZYGOTE;

MURINAE;

EID: 0037466457     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-291X(03)00537-0     Document Type: Article

References (44)

1. Pedersen R.A., Burdsal G.A. Mammalian embryogenesis. Knobil E., Neill D. The Physiology of Reproduction. second ed. 1994;319-390 Raven Press, New York.
2. Nothias J.Y., Majumder S., Kaneko K.J.et al. Regulation of gene expression at the beginning of mammalian development. J. Biol. Chem. 270:1995;22077-22080.
3. Flach G., Johnson M.H., Braude P.R.et al. The transition from maternal to embryonic control in the 2-cell mouse embryo. EMBO J. 1:1982;681-686.
4. Braude P., Bolton V., Moore S. Human gene expression first occurs between the four- and eight-cell stage of preimplantation development. Nature. 332:1988;459-461.
5. Camous S., Kopecny V., Flechon J.E. Autoradiographic detection of the earliest stage of 3H-uridine incorporation into the cow embryo. Biol. Cell. 58:1986;195-200.
6. Telford T.A., Watson A.J., Schultz G.A. Transition from maternal to embryonic control in early mammalian development: a comparison of several species. Mol. Reprod. Dev. 26:1990;90-100.
7. Ram P.T., Schultz R.M. Reporter gene expression in G2 of the 1-cell mouse embryo. Dev. Biol. 156:1993;552-556.
8. Latham K.E. Mechanisms and control of embryonic genome activation in mammalian embryos. Int. Rev. Cytol. 193:1999;71-124.
9. Gagne M., Pothier F., Sirard M.A. Foreign gene expression in activated oocytes and bovine embryos following pAGS-lacZ plasmid microinjection. Theriogenology. 39:1993;223.
10. Christians E., Rao V.H., Renard J.P. Sequential acquisition of transcriptional control during early embryonic development in the rabbit. Dev. Biol. 164:1994;160-172.
11. Lee K.F., Chow J.F.C., Xu J.S.et al. A comparative study of gene expression in murine embryos developed in vivo, cultured in vitro and cocultured with human oviductal cells using messenger ribonucleic acid differential display. Biol. Reprod. 64:2001;910-917.
12. Chow J.F.C., Lee K.F., Chan S.T.H.et al. Quantification of transforming growth factor β1 (TGF β1) mRNA expression in mouse peimplantation embryos and determination of TGFβ receptor (type I and type II) expression in mouse embryos and reproductive tract. Mol. Hum. Reprod. 7:2001;1047-1056.
13. Lee K.F., Kwok K.L., Yeung W.S.B. Suppression subtractive hybridization identifies genes expression in oviduct during mouse preimplantation period. Biochem. Biophys. Res. Commun. 277:2000;680-685.
14. Lee K.F., Yao Y.Q., Kwok K.L.et al. Early developing embryos affect the gene expression patterns in the mouse oviduct. Biochem. Biophys. Res. Commun. 292:2002;564-670.
15. Altschul S.F., Gish W., Miller W., Myers E.W., Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 215:1990;403-410.
16. Howlett S.K., Bolton V.N. Sequence and regulation of morphological and molecular events during the first cell cycle of mouse embryogenesis. J. Embryol. Exp. Morphol. 87:1985;175-206.
17. Latham K.E., Solter D., Schultz R.M. Acquisition of transcriptionally permissive state during the one-cell stage of mouse embryogenesis. Dev. Biol. 149:1992;457-462.
18. Ferreira J., Carmo-Fonseca M. Genome replication in early mouse embryos follows a defined temporal and spatial order. J. Cell Sci. 110:1997;889-897.
19. Aoki F., Worrad D.M., Schultz R.M. Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo. Dev. Biol. 181:1997;296-307.
20. Wiekowski M., Miranda M., Nothias J.Y.et al. Changes in histone synthesis and modification at the beginning of mouse development correlate with the establishment of chromatin mediated repression of transcription. J. Cell Sci. 110:1997;1147-1158.
21. Fiddler M., Abdel-Rahman B., Rappolee D.A.et al. Expression of SRY transcripts in preimplantation human embryos. Am. J. Med. Genet. 55:1995;80-84.
22. Ao A., Erickson R.P., Winston R.M.et al. Transcription of paternal Y-linked genes in the human zygote as early as the pronucleate stage. Zygote. 2:1994;281-288.
23. PeiL L., Melmed S. Isolation and characterization of a pituitary tumor-transforming gene (PTTG). Mol. Endocrinol. 11:1997;433-441.
24. Dominguez A., Ramos-Morales F., Romero F.et al. Hpttg a human homologue of rat pttg, is overexpressed in hematopoietic neoplasms. Evidence for a transcriptional activation function of hPTTG. Oncogene. 17:1998;2187-2193.
25. Zhang X., Horwitz G.A., Prezant T.R.et al. Structure, expression, and function of human pituitary tumor-transforming gene (PTTG). Mol. Endocrinol. 13:1999;156-166.
26. Chien W., Pei L. A novel binding factor facilitates nuclear translocation and transcriptional activation function of the pituitary tumor-transforming gene product. J. Biol. Chem. 275:2000;19422-19427.
27. Pei L. Identification of c-myc as a down-stream target for pituitary tumor-transforming gene. J. Biol. Chem. 276:2001;8484-8491.
28. Pei L. Activation of mitogen-activated protein kinase cascade regulates pituitary tumor-transforming gene transactivation function. J. Biol. Chem. 275:2000;31191-31198.
29. Pei L. Genomic organization and identification of an enhancer element containing binding sites for multiple proteins in rat pituitary tumor-transforming gene. J. Biol. Chem. 273:1998;5219-5225.
30. Dynan W.S., Sazer S., Tjian R.et al. Transcription factor Sp1 recognizes a DNA sequence in the mouse dihydrofolate reductase promoter. Nature. 319:1986;246-248.
31. Kadonaga J.T., Tjian R. Affinity purification of sequence-specific DNA binding proteins. Proc. Natl. Acad. Sci. USA. 83:1986;5889-5893.
32. Worrad D.M., Ram P.T., Schultz R.M. Regulation of gene expression in the mouse oocyte and early preimplantation embryo: developmental changes in Sp1 and TATA box-binding protein, TBP. Development. 120:1994;2347-2357.
33. Pei L. Pituitary tumor-transforming gene protein associates with ribosomal protein S10 and a novel human homologue of Dna J in testicular cells. J. Biol. Chem. 274:1999;3151-3158.
34. Oh B., Hwang S.Y., McLaughlin J.et al. Timely transiation during the mouse oocyte-to-embryo transition. Development. 127:2000;3795-3803.
35. Oh B., Hwang S.Y., Solter D.et al. Spindlin, a major maternal transcript expressed in the mouse during the transition from oocyte to embryo. Development. 124:1997;493-503.
36. Haynes S.R., Dollard C., Winston F.et al. The bromodomain: a conserved sequence found in human, Drosophila and yeast proteins. Nucleic Acids Res. 20:1992;2603.
37. Jeanmougin F., Wurtz J., Le Douarin B.et al. The bromodomain revisited. Trends Biochem. Sci. 22:1997;151-153.
38. Cuppen E., van Ham M., Pepers B.et al. Identification and molecular characterization of BP75, a novel bromodomain-containing protein. FEBS Lett. 459:1999;291-298.
39. Chishti A.H., Kim A.C., Marfatia S.M.et al. The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane. Trends Biochem. Sci. 23:1998;281-282.
40. Sato N., Funayama N., Nagafuchi A.et al. A gene family consisting of ezrin, radixin and moesin. Its specific localization at actin filament/plasma membrane association sites. J. Cell Sci. 103:1992;131-143.
41. Tsukita S., Yonemura S. Cortical actin organization: lessons from ERM (ezrin/radixin/moesin) proteins. J. Biol. Chem. 274:1999;34507-34510.
42. Angerth T., Huang R.Y., Aveskogh M.et al. Cloning and structural analysis of a gene encoding a mouse mastocytoma proteoglycan core protein; analysis of its evolutionary relation to three cross hybridizing regions in the mouse genome. Gene. 93:1990;235-240.
43. Sali A., Matsumoto R., McNeil H.P.et al. Three-dimensional models of four mouse mast cell chymases: identification of proteoglycan binding regions and protease-specific antigenic epitopes. J. Biol. Chem. 268:1993;9023-9034.
44. Ho H.C., McGrath K.E., Brodbeck K.C.et al. Serglycin proteoglycan synthesis in the murine uterine decidua and early embryo. Biol. Reprod. 62:2001;1667-1676.