Effects of Thioglycolic Acid on Progesterone-Induced Maturation of Xenopus Oocytes

REFERENCES

• Abrieu, A., Doree, M., and Fisher, D., 2001. The interplay between cyclin-B-Cdc2 kinase (MPF) and MAP kinase during maturation of oocytes, J. Cell Sci. 114 (2001), pp. 257–267.
   PubMed Web of Science ®Google Scholar
• Andersen, S. S., Buendia, B., Dominguez, J. E., Sawyer, A., and Karsenti, E., 1994. Effect on microtubule dynamics of XMAP230, a microtubule-associated protein present in Xenopus laevis eggs and dividing cells, J. Cell Biol. 127 (1994), pp. 1289–1299.
   PubMed Web of Science ®Google Scholar
• Becker, B. E., and Gard, D. L., 2006. Visualization of the cytoskeleton in Xenopus oocytes and eggs by confocal immunofluorescence microscopy, Methods Mol. Biol. 322 (2006), pp. 69–86.
   PubMedGoogle Scholar
• Bodart, J. F., Gutierrez, D. V., Nebreda, A. R., Buckner, B. D., Resau, J. R., and Duesbery, N. S., 2002. Characterization of MPF and MAPK activities during meiotic maturation of Xenopus tropicalis oocytes, Dev. Biol. 245 (2002), pp. 348–361.
   PubMed Web of Science ®Google Scholar
• Brunet, S., and Maro, B., 2005. Cytoskeleton and cell cycle control during meiotic maturation of the mouse oocyte: Integrating time and space, Reproduction 130 (2005), pp. 801–811.
   PubMed Web of Science ®Google Scholar
• Castro, A., Peter, M., Lorca, T., and Mandart, E., 2001. c-Mos and cyclin B/cdc2 connections during Xenopus oocyte maturation, Biol. Cell 93 (2001), pp. 15–25.
   PubMed Web of Science ®Google Scholar
• Cha, B., Cassimeris, L., and Gard, D. L., 1999. XMAP230 is required for normal spindle assembly in vivo and in vitro, J. Cell Sci. 112 (1999), pp. 4337–4346.
   PubMed Web of Science ®Google Scholar
• Dumont, J. N., 1972. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals, J. Morphol. 136 (1972), pp. 153–179.
   PubMed Web of Science ®Google Scholar
• Dunphy, W. G., Brizuela, L., Beach, D., and Newport, J., 1988. The Xenopus cdc2 protein is a component of MPF, a cytoplasmic regulator of mitosis, Cell 54 (1988), pp. 423–431.
   PubMed Web of Science ®Google Scholar
• Eliscovich, C., Peset, I., Vernos, I., and Mendez, R., 2008. Spindle-localized CPE-mediated translation controls meiotic chromosome segregation, Nat. Cell Biol. 10 (2008), pp. 858–865.
   PubMed Web of Science ®Google Scholar
• Ferrell, J. E., 1999. Xenopus oocyte maturation: New lessons from a good egg, Bioessays 21 (1999), pp. 833–842.
   PubMed Web of Science ®Google Scholar
• Ferrell, J. E., and Machleder, E. M., 1998. The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes, Science 280 (1998), pp. 895–898.
   PubMed Web of Science ®Google Scholar
• Fisher, D. L., Brassac, T., Galas, S., and Doree, M., 1999. Dissociation of MAP kinase activation and MPF activation in hormone-stimulated maturation of Xenopus oocytes, Development 126 (1999), pp. 4537–4546.
   PubMed Web of Science ®Google Scholar
• Frank-Vaillant, M., Jessus, C., Ozon, R., Maller, J. L., and Haccard, O., 1999. Two distinct mechanisms control the accumulation of cyclin B1 and Mos in Xenopus oocytes in response to progesterone, Mol. Biol. Cell 10 (1999), pp. 3279–3288.
   PubMed Web of Science ®Google Scholar
• Furuno, N., Nishizawa, M., Okazaki, K., Tanaka, H., Iwashita, J., Nakajo, N., Ogawa, Y., and Sagata, N., 1994. Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes, EMBO J. 13 (1994), pp. 2399–2410.
   PubMed Web of Science ®Google Scholar
• Gaffre, M., Dupre, A., Valuckaite, R., Suziedelis, K., Jessus, C., and Haccard, O., 2006. Deciphering the H-Ras pathway in Xenopus oocyte, Oncogene. 25 (2006), pp. 5155–5162.
   PubMed Web of Science ®Google Scholar
• Gan, H. F., Meng, X. S., Song, C. H., and Li, B. X., 2003. A survey on health effects in a human population exposed to permanent-waving solution containing thioglycolic acid, J. Occup. Health 45 (2003), pp. 400–404.
   PubMed Web of Science ®Google Scholar
• Gard, D. L., Cha, B. J., and King, E., 1997. The organization and animal-vegetal asymmetry of cytokeratin filaments in stage VI Xenopus oocytes is dependent upon F-actin and microtubules, Dev. Biol. 184 (1997), pp. 95–114.
   PubMed Web of Science ®Google Scholar
• Gautier, J., and Maller, J. L., 1991. Cyclin B in Xenopus oocytes: Implications for the mechanism of pre-MPF activation, EMBO J. 10 (1991), pp. 177–182.
   PubMed Web of Science ®Google Scholar
• Gotoh, Y., Masuyama, N., Dell, K., Shirakabe, K., and Nishida, E., 1995. Initiation of Xenopus oocyte maturation by activation of the mitogen-activated protein kinase cascade, J. Biol. Chem. 270 (1995), pp. 25898–25904.
   PubMed Web of Science ®Google Scholar
• Haccard, O., Lewellyn, A., Hartley, R. S., Erikson, E., and Maller, J. L., 1995. Induction of Xenopus oocyte meiotic maturation by MAP kinase, Dev. Biol. 168 (1995), pp. 677–682.
   PubMed Web of Science ®Google Scholar
• Hill, W. G., Southern, N. M., MacIver, B., Potter, E., Apodaca, G., Smith, C. P., and Zeidel, M. L., 2005. Isolation and characterization of the Xenopus oocyte plasma membrane: A new method for studying activity of water and solute transporters, Am. J. Physiol. Renal Physiol. 289 (2005), pp. F217–F224.
   PubMed Web of Science ®Google Scholar
• Hirshfield, A. N., 1997. Overview of ovarian follicular development: considerations for the toxicologist, Environ. Mol. Mutagen. 29 (1997), pp. 10–15.
   PubMed Web of Science ®Google Scholar
• Hou, S. Y., Zhang, L., Xia, L., and Wu, K., 2008. Thioglycolic acid inhibits mouse oocyte maturation and affects chromosomal arrangement and spindle configuration, Toxicol. Ind. Health 24 (2008), pp. 227–234.
   PubMed Web of Science ®Google Scholar
• Jin, X. Y., Yin, X. H., and Jin, F. L., 1999. Survey and intervention analysis of hairdressers, J. Hyg. Res. 28 (1999), pp. 25–26.
   Google Scholar
• Kersemaekers, W. M., Roeleveld, N., and Zielhuis, G. A., 1995. Reproductive disorders due to chemical exposure among hairdressers, Scand. J. Work Environ. Health 21 (1995), pp. 325–334.
   PubMed Web of Science ®Google Scholar
• Kersemaekers, W. M., Roeleveld, N., and Zielhuis, G. A., 1997. Reproductive disorders among hairdressers, Epidemiology 8 (1997), pp. 396–401.
   PubMed Web of Science ®Google Scholar
• Klymkowsky, M. W., and Maynell, L. A., 1989. MPF-induced breakdown of cytokeratin filament organization in the maturing Xenopus oocyte depends upon the translation of maternal mRNAs, Dev Biol. 134 (1989), pp. 479–485.
   PubMed Web of Science ®Google Scholar
• Kobayashi, H., Minshull, J., Ford, C., Golsteyn, R., Poon, R., and Hunt, T., 1991. On the synthesis and destruction of A- and B-type cyclins during oogenesis and meiotic maturation in Xenopus laevis, J. Cell Biol. 114 (1991), pp. 755–765.
   PubMed Web of Science ®Google Scholar
• Ma, C., Benink, H. A., Cheng, D., Montplaisir, V., Wang, L., Xi, Y., Zheng, P. P., Bement, W. M., and Liu, X. J., 2006. Cdc42 activation couples spindle positioning to first polar body formation in oocyte maturation, Curr Biol. 16 (2006), pp. 214–220.
   PubMed Web of Science ®Google Scholar
• Maller, J. L., Schwab, M. S., Roberts, B. T., Gross, S. D., Taieb, F. E., and Tunquist, B. J., 2001. The pathway of MAP kinase mediation of CSF arrest in Xenopus oocytes, Biol. Cell. 93 (2001), pp. 27–33.
   PubMed Web of Science ®Google Scholar
• Masui, Y., 2001. From oocyte maturation to the in vitro cell cycle: The history of discoveries of maturation-promoting factor (MPF) and cytostatic factor (CSF), Differentiation 69 (2001), pp. 1–17.
   PubMed Web of Science ®Google Scholar
• Minshull, J., Sun, H., Tonks, N. K., and Murray, A. W., 1994. A MAP kinase-dependent spindle assembly checkpoint in Xenopus egg extracts, Cell 79 (1994), pp. 475–486.
   PubMed Web of Science ®Google Scholar
• Palmer, A., Gavin, A. C., and Nebreda, A. R., 1998. A link between MAP kinase and p34(cdc2)/cyclin B during oocyte maturation: p90(rsk) phosphorylates and inactivates the p34(cdc2) inhibitory kinase Myt1, EMBO J. 17 (1998), pp. 5037–5047, .
   PubMed Web of Science ®Google Scholar
• Peter, M., Castro, A., Lorca, T., Le Peuch, C., Magnaghi-Jaulin, L., Doree, M., and Labbe, J. C., 2001. The APC is dispensable for first meiotic anaphase in Xenopus oocytes, Nat. Cell Biol. 3 (2001), pp. 83–87.
   PubMed Web of Science ®Google Scholar
• Peter, M., Labbe, J. C., Doree, M., and Mandart, E., 2002. A new role for Mos in Xenopus oocyte maturation: Targeting Myt1 independently of MAPK, Development 129 (2002), pp. 2129–2139.
   PubMed Web of Science ®Google Scholar
• Qian, Y. W., Erikson, E., Taieb, F. E., and Maller, J. L., 2001. The polo-like kinase Plx1 is required for activation of the phosphatase Cdc25C and cyclin B-Cdc2 in Xenopus oocytes, Mol. Biol. Cell. 12 (2001), pp. 1791–1799.
   PubMed Web of Science ®Google Scholar
• Roy, L. M., Haccard, O., Izumi, T., Lattes, B. G., Lewellyn, A. L., and Maller, J. L., 1996. Mos proto-oncogene function during oocyte maturation in Xenopus, Oncogene 12 (1996), pp. 2203–2211.
   PubMed Web of Science ®Google Scholar
• Rylander, L., Axmon, A., Toren, K., and Albin, M., 2002. Reproductive outcome among female hairdressers, Occup. Environ. Med. 59 (2002), pp. 517–522.
   PubMed Web of Science ®Google Scholar
• Shiina, N., Moriguchi, T., Ohta, K., Gotoh, Y., and Nishida, E., 1992. Regulation of a major microtubule-associated protein by MPF and MAP kinase, EMBO J. 11 (1992), pp. 3977–3984.
   PubMed Web of Science ®Google Scholar
• Song, C. H., and Gan, H. F., 1990. A study on toxicity and mutagenicity of thioglycolic acid through percutaneous administration, Ind Health Occup Dis 16 (1990), pp. 145–148.
   Google Scholar
• Stebbins-Boaz, B., Fortner, K., Frazier, J., Piluso, S., Pullen, S., Rasar, M., Reid, W., Sinclair, K., and Winger, E., 2004. Oocyte maturation in Xenopus laevis is blocked by the hormonal herbicide, 2,4-dichlorophenoxy acetic acid, Mol. Reprod. Dev. 67 (2004), pp. 233–242.
   PubMed Web of Science ®Google Scholar
• Taieb, F. E., Gross, S. D., Lewellyn, A. L., and Maller, J. L., 2001. Activation of the anaphase-promoting complex and degradation of cyclin B is not required for progression from Meiosis I to II in Xenopus oocytes, Curr Biol. 11 (2001), pp. 508–513.
   PubMed Web of Science ®Google Scholar
• Takenaka, K., Gotoh, Y., and Nishida, E., 1997. MAP kinase is required for the spindle assembly checkpoint but is dispensable for the normal M phase entry and exit in Xenopus egg cell cycle extracts, J. Cell Biol. 136 (1997), pp. 1091–1097.
   PubMed Web of Science ®Google Scholar
• Zhang, G., and Song, C. H., 1990. Effect of TGA on pathology and ultrastructure of testes and ovaries in rats by smearing on skin, J. Health Toxicol. 4 (1990), pp. 89–91.
   Google Scholar