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将已知序列的DNA注射到非洲爪蟾的卵和卵母细胞后进行转录。

Transcription of DNAs of known sequence after injection into eggs and oocytes of Xenopus laevis.

作者信息

Colman A

出版信息

Eur J Biochem. 1975 Sep 1;57(1):85-96. doi: 10.1111/j.1432-1033.1975.tb02279.x.

Abstract
  1. When the synthetic polynucleotide, poly[d(A-T) - d(A-T)] is injected into the eggs and oocytes of Xenopus laevis, a stimulation of RNA synthesis results. Analysis of extracted RNA by high-voltage electrophoresis, shows that this stimulation of RNA synthesis is due to the production of poly[r(A-U)] transcripts. The rate of poly[r(A-U)] synthesis is calculated to be at least ten-fold greater in eggs than in oocytes. The amount of poly[r(A-U)] detectable in injected eggs has reached a maximum by 1.5 h after injection; in oocytes, however, poly[r(A-U)] continues to accumulate between the third and 16th hour after injection. The transcripts range in length from less than 80 nucleotides up to over 2000 nucleotides long. The co-injection of poly[d(A-T)] - d(A-T)] and alpha-amanitin into oocytes, has shown that the synthesis of poly[r(A-U)] is approximately 90% inhibited at a concentration of alpha-amanitin which has no effect on the capacity of the oocyte to synthesize ribosomal and 4-S RNA; thus the nucleoplasmic RNA polymerases IIa and/or IIb, are implicated as playing a major role in poly[r(A-U)] synthesis in oocytes. 2. When poly(dG) - poly(d-C), poly(dA), poly(dA) - poly(dT) and poly[d(I-C) - d(I-C)] are individually injected into eggs only poly[d(I-C) - d(I-C)] is transcribed as efficiently as poly[d(A-T) - d(A-T)]. 3. When calf thymus native or denatured DNA, polyoma, T2, T4 and phiX DNAs are individually injected into eggs only the injection of calf thymus native DNA causes a detectable stimulation of RNA synthesis. 4. The activities of crude preparations of egg and oocyte RNA polymerases are tested in vitro with different DNA templates. In contrast to the situation in vivo, it is found that poly[d(A-T1 - d(A-T)] is as efficiently transcribed in vitro by oocyte polymerase as by egg polymerase. Additionally poly[d(A-T) - d(A-T)] is transcribed ten-fold more efficiently in vitro than calf thymus native DNA. When poly(dA) - poly(dT), poly(dA), phiX, T2, and calf thymus denatured DNA are tested in vitro, only calf thymus denatured DNA is transcribed to a significant extent. The above results are discussed in relation to the known synthetic activities of Xenopus eggs and oocytes.
摘要
  1. 当将合成多聚核苷酸聚[d(A-T)-d(A-T)]注入非洲爪蟾的卵和卵母细胞时,会导致RNA合成受到刺激。通过高压电泳对提取的RNA进行分析表明,这种RNA合成的刺激是由于产生了聚[r(A-U)]转录本。计算得出,卵中聚[r(A-U)]的合成速率比卵母细胞中至少高10倍。在注入后1.5小时,注入卵中可检测到的聚[r(A-U)]量已达到最大值;然而,在卵母细胞中,聚[r(A-U)]在注入后第3小时到第16小时之间持续积累。转录本的长度范围从不到80个核苷酸到超过2000个核苷酸。将聚[d(A-T)-d(A-T)]和α-鹅膏蕈碱共同注入卵母细胞表明,在对卵母细胞合成核糖体RNA和4-S RNA的能力没有影响的α-鹅膏蕈碱浓度下,聚[r(A-U)]的合成约被抑制90%;因此,核质RNA聚合酶IIa和/或IIb被认为在卵母细胞中聚[r(A-U)]的合成中起主要作用。2. 当将聚(dG)-聚(dC)、聚(dA)、聚(dA)-聚(dT)和聚[d(I-C)-d(I-C)]分别注入卵中时,只有聚[d(I-C)-d(I-C)]的转录效率与聚[d(A-T)-d(A-T)]一样高。3. 当将小牛胸腺天然或变性DNA、多瘤病毒、T2、T4和φX DNA分别注入卵中时,只有注入小牛胸腺天然DNA会引起可检测到的RNA合成刺激。4. 用不同的DNA模板在体外测试卵和卵母细胞RNA聚合酶粗制品的活性。与体内情况相反,发现聚[d(A-T)-d(A-T)]在体外被卵母细胞聚合酶转录的效率与被卵聚合酶转录的效率一样高。此外,聚[d(A-T)-d(A-T)]在体外被转录的效率比小牛胸腺天然DNA高10倍。当在体外测试聚(dA)-聚(dT)、聚(dA)、φX、T2和小牛胸腺变性DNA时,只有小牛胸腺变性DNA被大量转录。以上结果结合非洲爪蟾卵和卵母细胞已知的合成活性进行了讨论。

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