Quantification of housekeeping transcript levels during the development of bovine preimplantation embryos

Biology of Reproduction

Volumn 67, Issue 5, 2002, Pages 1465-1472

  Robert, Claude ^a   McGraw, Serge ^a   Massicotte, Lyne ^a   Pravetoni, Marco ^a   Gandolfi, Fulvio ^a   Sirard, Marc André ^a  

^a UNIVERSITÉ LAVAL   (Canada)

Author keywords

Developmental biology; Early development; Embryo; Oocyte development; Ovum

Indexed keywords

ANALYTIC METHOD; ANIMAL TISSUE; ARTICLE; COMPETITIVE INHIBITION; DEVELOPMENTAL BIOLOGY; DNA TEMPLATE; EMBRYO DEVELOPMENT; GENE EXPRESSION REGULATION; GENETIC TRANSCRIPTION; HOUSEKEEPING GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; PROMOTER REGION; SECOND MESSENGER; TRANSCRIPTION REGULATION; ANIMAL; BLASTOCYST; CATTLE; FEMALE; GENETICS; METABOLISM; METHODOLOGY; NUCLEIC ACID PROBE; PHYSIOLOGY; PREGNANCY; STANDARD;

ANIMALIA; BOVINAE; MAMMALIA;

ACTIN; HISTONE; LAMIN B; MESSENGER RNA; RNA 18S; SMALL NUCLEAR RNA; TUBULIN; U2 SMALL NUCLEAR RNA; UBIQUITIN;

ACTINS; ANIMALS; ANTISENSE ELEMENTS (GENETICS); BLASTOCYST; CATTLE; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HISTONES; LAMIN TYPE B; POLYMERASE CHAIN REACTION; PREGNANCY; PROMOTER REGIONS (GENETICS); RNA, MESSENGER; RNA, RIBOSOMAL, 18S; RNA, SMALL NUCLEAR; TRANSCRIPTION, GENETIC; TUBULIN; UBIQUITIN;

EID: 0036839114     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod.102.006320     Document Type: Article

References (43)

1. Watson AJ, Wiemer KE, Arcellana-Panlilio M, Schultz GA. U2 small nuclear RNA localization and expression during bovine preimplantation development. Mol Reprod Dev 1992; 31:231-240.
2. Bilodeau-Goeseels S, Schultz GA. Changes in the relative abundance of various housekeeping gene transcripts in in vitro-produced early bovine embryos. Mol Reprod Dev 1997; 47:413-420.
3. Gaudette MF, Cao QP, Crain WR. Quantitative analysis of specific messenger RNAs in small numbers of preimplantation embryos. Methods Enzymol 1993; 225:328-344.
4. Watson AJ, Hogan A, Hahnel A, Wiemer KE, Schultz GA. Expression of growth factor ligand and receptor genes in the preimplantation bovine embryo. Mol Reprod Dev 1992; 31:87-95.
5. Gutierrez-Adan A, Behboodi E, Murray JD, Anderson GB. Early transcription of the SRY gene by bovine preimplantation embryos. Mol Reprod Dev 1997; 48:246-250.
6. Lighten AD, Hardy K, Winston RM, Moore GE. Expression of mRNA for the insulin-like growth factors and their receptors in human preimplantation embryos. Mol Reprod Dev 1997; 47:134-139.
7. Zhang X, Kidder GM, Zhang C, Khamsi F, Armstrong DT. Expression of plasminogen activator genes and enzymatic activities in rat preimplantation embryos. J Reprod Fertil 1994; 101:235-240.
8. Roelen BA, Van Eijk MJ, Van Rooijen MA, Bevers MM, Larson JH, Lewin HA, Mummery CL. Molecular cloning, genetic mapping, and developmental expression of a bovine transforming growth factor beta (TGF-beta) type I receptor. Mol Reprod Dev 1998; 49:1-9.
9. Wrenzycki C, Herrmann D, Carnwath JW, Niemann H. Expression of RNA from developmentally important genes in preimplantation bovine embryos produced in TCM supplemented with BSA. J Reprod Fertil 1998; 112:387-398.
10. Edashige K, Sakamoto M, Kasai M. Expression of mRNAs of the aquaporin family in mouse oocytes and embryos. Cryobiology 2000; 40:171-175.
11. Izadyar F, Zhao J, Van Tol HT, Colenbrander B, Bevers MM. Messenger RNA expression and protein localization of growth hormone in bovine ovarian tissue and in cumulus oocyte complexes (COCs) during in vitro maturation. Mol Reprod Dev 1999; 53:398-406.
12. Taylor DM, Ray PF, Ao A, Winston RM, Handyside AH. Paternal transcripts for glucose-6-phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the three- to four-cell stage. Mol Reprod Dev 1997; 48:442-448.
13. Lequarre AS, Grisart B, Moreau B, Schuurbiers N, Massip A, Dessy F. Glucose metabolism during bovine preimplantation development: Analysis of gene expression in single oocytes and embryos. Mol Reprod Dev 1997; 48:216-226.
14. Temeles GL, Ram PT, Rothstein JL, Schultz RM. Expression patterns of novel genes during mouse preimplantation embryogenesis. Mol Reprod Dev 1994; 37:121-129.
15. Davis W Jr, De Sousa PA, Schultz RM. Transient expression of translation initiation factor eIF-4C during the 2-cell stage of the preimplantation mouse embryo: Identification by mRNA differential display and the role of DNA replication in zygotic gene activation. Dev Biol 1996; 174:190-201.
16. De Sousa PA, Westhusin ME, Watson AJ. Analysis of variation in relative mRNA abundance for specific gene transcripts in single bovine oocytes and early embryos. Mol Reprod Dev 1998; 49:119-130.
17. De Sousa PA, Watson AJ, Schultz RM. Transient expression of a translation initiation factor is conservatively associated with embryonic gene activation in murine and bovine embryos. Biol Reprod 1998; 59:969-977.
18. Wrenzycki C, Herrmann D, Carnwath JW, Niemann H. Alterations in the relative abundance of gene transcripts in preimplantation bovine embryos cultured in medium supplemented with either serum or PVA. Mol Reprod Dev 1999; 53:8-18.
19. Ma J, Svoboda P, Schultz RM, Stein P. Regulation of zygotic gene activation in the preimplantation mouse embryo: Global activation and repression of gene expression. Biol Reprod 2001; 64:1713-1721.
20. Riego E, Perez A, Martinez R, Castro FO, Lleonart R, de la Fuente J. Differential constitutive expression of interferon genes in early mouse embryos. Mol Reprod Dev 1995: 41:157-166.
21. Fleming JV, Fontanier N, Harries DN, Rees WD. The growth arrest genes gas5, gas6, and CHOP-10 (gadd153) are expressed in the mouse preimplantation embryo. Mol Reprod Dev 1997; 48:310-316.
22. Fontanier-Razzaq N, McEvoy TG, Robinson JJ, Rees WD. DNA damaging agents increase gadd153 (CHOP-10) messenger RNA levels in bovine preimplantation embryos cultured in vitro. Biol Reprod 2001; 64:1386-1391.
23. Bieser B, Stojkovic M, Wolf E, Meyer H, Einspanier R. Growth factors and components for extracellular proteolysis are differentially expressed during in vitro maturation of bovine cumulus-oocyte complexes. Biol Reprod 1998; 59:801-806.
24. Krussel JS, Huang HY, Simon C, Behr B, Pape AR, Wen Y, Bielfeld P, Polan ML. Single blastomeres within human preimplantation embryos express different amounts of messenger ribonucleic acid for beta-actin and interleukin-1 receptor type I. J Clin Endocrinol Metab 1998; 83:953-959.
25. Moley KH, Chi MM, Mueckler MM. Maternal hyperglycemia alters glucose transport and utilization in mouse preimplantation embryos. Am J Physiol 1998; 275:E38-E47.
26. Anderson JE, Matteri RL, Abeydeera LR, Day BN, Prather RS. Cyclin B1 transcript quantitation over the maternal to zygotic transition in both in vivo- and in vitro-derived 4-cell porcine embryos. Biol Reprod 1999; 61:1460-1467.
27. Navarrete Santos A, Augustin R, Lazzari G, Galli C, Sreenan JM, Fischer B. The insulin-dependent glucose transporter isoform 4 is expressed in bovine blastocysts. Biochem Biophys Res Commun 2000; 271:753-760.
28. Bustin SA. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J Mol Endocrinol 2000; 25:169-193.
29. Steuerwald N, Cohen J, Herrera RJ, Brenner CA. Analysis of gene expression in single oocytes and embryos by real-time rapid cycle fluorescence monitored RT-PCR. Mol Hum Reprod 1999; 5:10341039.
30. Steuerwald N, Barritt JA, Adler R, Malter H, Schimmel T, Cohen J, Brenner CA. Quantification of mtDNA in single oocytes, polar bodies and subcellular components by real-time rapid cycle fluorescence monitored PCR. Zygote 2000; 8:209-215.
31. Steuerwald N, Cohen J, Herrera RJ, Brenner CA. Quantification of mRNA in single oocytes and embryos by real-time rapid cycle fluorescence monitored RT-PCR. Mol Hum Reprod 2000; 6:448-453.
32. Blondin P, Sirard MA. Oocyte and follicular morphology as determining characteristics for developmental competence in bovine oocytes. Mol Reprod Dev 1995; 41:54-62.
33. Holm P, Booth PJ, Schmidt MH, Greve T, Callesen H. High bovine blastocyst development in a static in vitro production system using SOFaa medium supplemented with sodium citrate and myo-inositol with or without serum-proteins. Theriogenology 1999; 52:683-700.
34. Ali A, Sirard MA. Effect of the absence or presence of various protein supplements on further development of bovine oocytes during in vitro maturation. Biol Reprod 2002; 66:901-905.
35. Phillips J, Eberwine JH. Antisense RNA amplification: a linear amplification method for analyzing the mRNA population from single living cells. Methods 1996; 10:283-288.
36. Luo L, Salunga RC, Guo H, Bittner A, Joy KC, Galindo JE, Xiao H, Rogers KE, Wan JS, Jackson MR, Erlander MG. Gene expression profiles of laser-captured adjacent neuronal subtypes. Nat Med 1999; 5:117-122.
37. Memili E, Dominko T, First NL. Onset of transcription in bovine oocytes and preimplantation embryos. Mol Reprod Dev 1998; 51:36-41.
38. Bachvarova RF. A maternal tail of poly(A): The long and the short of it. Cell 1992; 69:895-897.
39. Paynton BV, Bachvarova R. Polyadenylation and deadenylation of maternal mRNAs during oocyte growth and maturation in the mouse. Mol Reprod Dev 1994; 37:172-178.
40. Rodman TC, Bachvarova R. RNA synthesis in preovulatory mouse oocytes. J Cell Biol 1976; 70:251-257.
41. Meric F, Searfoss AM, Wormington M, Wolffe AP. Masking and unmasking maternal mRNA. The role of polyadenylation, transcription, splicing, and nuclear history. J Biol Chem 1996; 271:30804-30810.
42. Brevini-Gandolfi TA, Favetta LA, Mauri L, Luciano AM, Cillo F, Gandolfi F. Changes in poly(A) tail length of maternal transcripts during in vitro maturation of bovine oocytes and their relation with developmental competence. Mol Reprod Dev 1999; 52:427-433.
43. Gandolfi TA, Gandolfi F. The maternal legacy to the embryo: Cytoplasmic components and their effects on early development. Theriogenology 2001; 55:1255-1276.