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SV40晚期mRNA剪接的电子显微镜证据。

Electron microscopic evidence for splicing of SV40 late mRNAs.

作者信息

Bratosin S, Horowitz M, Laub O, Aloni Y

出版信息

Cell. 1978 Apr;13(4):783-90. doi: 10.1016/0092-8674(78)90228-3.

Abstract

Poly(A)-containing SV40 cytoplasmic RNA was hybridized with linear double-stranded SV40 DNA and formed RNA displacement loops (R loops). The structures visualized in the electron microscope are consistent with the conclusion that the leader sequences at the 5' ends of the 16S and 19S late mRNAs are not coded immediately adjacent to the main portions of the mRNAs. These data are consistent with either segmentation of the leaders or heterogeneity of their lengths. Measurements carried out on the R loop structures have provided the locations, on the physical map of SV40 DNA, for the bodies and leaders of the 16S and 19S late mRNAs, and the lengths of the bodies, leaders and the corresponding intervening DNA sequences.

摘要

将含有多聚腺苷酸(Poly(A))的SV40细胞质RNA与线性双链SV40 DNA杂交,形成RNA置换环(R环)。在电子显微镜下观察到的结构与以下结论一致:16S和19S晚期mRNA 5'端的前导序列并非紧邻mRNA的主要部分编码。这些数据与前导序列的分段或长度异质性相符。对R环结构进行的测量给出了16S和19S晚期mRNA的主体、前导序列以及相应间隔DNA序列在SV40 DNA物理图谱上的位置,以及主体、前导序列的长度。

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