首页> 美国卫生研究院文献>Biochemical Journal >Differential sensitization to deoxyribonuclease I of Xenopus vitellogenin and albumin genes during primary and secondary induction of vitellogenesis by oestradiol.
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Differential sensitization to deoxyribonuclease I of Xenopus vitellogenin and albumin genes during primary and secondary induction of vitellogenesis by oestradiol.

机译:在雌二醇对卵黄发生的一次和二次诱导过程中非洲爪蟾卵黄蛋白原和白蛋白基因对脱氧核糖核酸酶I的差异性敏化。

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摘要

The sensitivity to DNAase (deoxyribonuclease) I (which preferentially digests transcribed sequences) of vitellogenin and albumin genes in liver and erythrocytes of male Xenopus after primary and secondary induction of vitellogenesis by oestrogen was measured by hybridization to cDNA (complementary DNA) of the residual DNA after enzymic digestion of isolated nuclei. Vitellogenin sequences were rendered selectively more sensitive to limited DNAase-I digestion (15-20% of DNA rendered acid-soluble) during primary hormonal activation (5 days) of vitellogenin genes in liver, but not erythrocyte, nuclei. Hormone withdrawal (25 days after first injection) did not result in reversion to a pre-activation gene configuration, nor did secondary hormonal stimulation (5 days after second and 25 days after first injection) augment the sensitivity of the genes to digestion by the nuclease. Similar hormone treatment did not affect the sensitivity of the constitutively expressed albumin genes in liver nuclei, nor their insensitivity in erythrocyte nuclei. Under the same conditions, globin genes remained indigestible in liver nuclei. It is concluded that primary induction of vitellogenesis in male Xenopus liver is accompanied by relatively long-lasting (3-4 weeks) change in the configuration of vitellogenin genes in hepatic nuclei which is not reversed or further modified during short-term oestrogen withdrawal or upon secondary stimulation.
机译:通过与残留DNA的cDNA(互补DNA)杂交,测定雄性非洲爪蟾肝细胞和红细胞中卵黄蛋白原和白蛋白基因的DNA酶(脱氧核糖核酸酶)I(优先消化转录的序列)对雄性非洲爪蟾肝脏和红细胞中卵黄蛋白原和白蛋白基因的敏感性。经过酶消化后分离出的细胞核。在肝脏中卵黄蛋白原基因(而非红细胞核)的初次激素激活(5天)期间,使卵黄蛋白原序列选择性地对有限的DNAase-I消化(15-20%的酸呈酸性)更敏感。激素撤药(第一次注射后25天)不会导致恢复到激活前的基因构型,二次激素刺激(第二次注射后5天和第一次注射后25天)也不会增加核酸酶对基因消化的敏感性。类似的激素处理既不影响组成型表达的白蛋白基因在肝核中的敏感性,也不影响它们在红细胞核中的不敏感性。在相同条件下,球蛋白基因在肝核中仍不可消化。结论是,雄性爪蟾肝脏中卵黄蛋白生成的初次诱导伴随着肝核中卵黄蛋白原基因构型的相对长期(3-4周)变化,在雌激素短期撤药时或在撤离后不会逆转或进一步修饰二次刺激。

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