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海星卵母细胞和胚胎中的二氢叶酸还原酶:甲氨蝶呤对其抑制的发育后果:(海星/二氢叶酸还原酶/甲氨蝶呤/DNA合成/早期发育)

Dihydrofolate Reductase in Starfish Oocytes and Embryos: Developmental Consequences of Its Inhibition by Methotrexate : (starfish/dihydrofolate reductase/methotrexate/DNA synthesis/early development).

作者信息

Ikegami Susumu, Imayoshi Junji, Takahashi Nobuo, Nagano Hiroshi

机构信息

Department of Applied Biochemistry, Hiroshima University, Fukuyama-shi, Hiroshima 720.

Department of Physiological Chemistry and Nutrition, Faculty of Medicine, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113, Japan.

出版信息

Dev Growth Differ. 1985;27(3):393-403. doi: 10.1111/j.1440-169X.1985.00393.x.

DOI:10.1111/j.1440-169X.1985.00393.x
PMID:37282145
Abstract

Dihydrofolate reductase in immature oocytes of the starfish, Asterina pectinifera, is estimated to be 12 pg per oocyte. After completion of meiosis, the quantity of the enzyme is approximately 20 pg per egg. The content of the enzyme in the egg is kept nearly constant at this value from fertilization to the beginning of blastulation. Methotrexate, an analogue of dihydrofolate, at 20 μM did not affect meiotic maturational process and fertilization, but inhibited embryonic development at the 512-cell stage which corresponds to the beginning of blastulation. Incorporation of externally supplied deoxy[ H]uridine into DNA of the embryos cultured in the continuous presence of 20 μM of methotrexate stopped at the 256-cell stage, suggesting that the cessassion of development of the embryo at the 512-cell stage was caused by inhibition of DNA synthesis at the preceding stage. Uptake of [ H]methotrexate was low at early cleavage stages but increased just before blastulation. Externally supplied 1 mM of thymidine counteracted the inhibitory effect of methotrexate at 20 μM, suggesting that the starvation of the methotrexate-treated embryo for thymidine nucleotides halted DNA synthesis at the beginning of blastulation.

摘要

海星(pectinifera海燕)未成熟卵母细胞中的二氢叶酸还原酶估计为每个卵母细胞12皮克。减数分裂完成后,每个卵子中该酶的量约为20皮克。从受精到囊胚形成开始,卵子中该酶的含量几乎保持在这个值不变。二氢叶酸类似物甲氨蝶呤在20 μM时不影响减数分裂成熟过程和受精,但在对应于囊胚形成开始的512细胞阶段抑制胚胎发育。在持续存在20 μM甲氨蝶呤的情况下培养的胚胎中,外部供应的脱氧[H]尿苷掺入DNA在256细胞阶段停止,这表明胚胎在512细胞阶段的发育停止是由前一阶段DNA合成的抑制引起的。在早期卵裂阶段,[H]甲氨蝶呤的摄取量较低,但在囊胚形成前增加。外部供应1 mM胸苷可抵消20 μM甲氨蝶呤的抑制作用,这表明经甲氨蝶呤处理的胚胎对胸苷核苷酸的缺乏在囊胚形成开始时停止了DNA合成。

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