Suppr超能文献

RNA肿瘤病毒的基因组组织II. 用限制性内切核酸酶对体外合成的莫洛尼鼠白血病病毒双链DNA的物理图谱

Genome organization of RNA tumor viruses II. Physical maps of in vitro-synthesized Moloney murine leukemia virus double-stranded DNA by restriction endonucleases.

作者信息

Verma I M, McKennett M A

出版信息

J Virol. 1978 Jun;26(3):630-45. doi: 10.1128/JVI.26.3.630-645.1978.

Abstract

Physical maps of the genome of Moloney murine leukemia virus (M-MLV) DNA were constructed by using bacterial restriction endonucleases. The in vitro-synthesized M-MLV double-stranded DNA was used as the source of the viral DNA. Restriction endonucleases Sal I and Hind III cleave viral DNA at only one site and, thus, generate two DNA fragments. The two DNA fragments generated by Sal I are Sal IA (molecular weight, 3.5 x 10(6)) and Sal IB (molecular weight, 2.4 x 10(6)) and by Hind III are Hind IIIA (molecular weight, 3.6 x 10(6) and Hind IIIB (molecular weight, 2.3 x 10(6)). Restriction endonuclease Bam I generates four fragments of molecular weights of 2.1 x 10(6) (Bam IA), 2 X 10(6) (Bam IB), 1.25 X 10(6) (Bam IC), and 0.24 x 10(6) (Bam ID), whereas restriction endonuclease Hpa I cleaves the M-MLV double-stranded DNA twice to give three fragments of molecular weights of 4.4 x 10(6) (Hpa IA), 0.84 X 10(6) (Hpa IB), and 0.74 x 10(6) (Hpa IC). Digestion of M-MLV double-stranded DNA with restriction endonuclease Sma I produces four fragments of molecular weights of 3.9 x 10(6) (Sma IA), 1.3 X 10(6) (Sma IB), 0.28 X 10(6) (Sma IC), and 0.21 x 10(6) (Sma ID). A mixture of restriction endonucleases Bgl I and Bgl II (Bgl I + II) cleaves the viral DNA at four sites generating five fragments of approximate molecular weights of 2 x 10(6) (Bgl + IIA), 1.75 X 10(6) (Bgl I + IIB), 1.25 X 10(6) (Bgl I + IIC), 0.40 X 10(6) (Bgl I + IID), and 0.31 x 10(6) (Bgl I + IIE). The order of the fragments in relation to the 5' end and 3' end of the genome was determined either by using fractional-length M-MLV double-stranded DNA for digestion by restriction endonucleases or by redigestion of Sal IA, Sal IB, Hind IIIA, and Hind IIIB fragments with other restriction endonucleases. In addition, a number of other restriction endonucleases that cleave in vitro-synthesized M-MLV double-stranded DNA have also been listed.

摘要

利用细菌限制性内切酶构建了莫洛尼鼠白血病病毒(M-MLV)DNA的物理图谱。体外合成的M-MLV双链DNA用作病毒DNA的来源。限制性内切酶Sal I和Hind III仅在一个位点切割病毒DNA,因此产生两个DNA片段。Sal I产生的两个DNA片段是Sal IA(分子量为3.5×10⁶)和Sal IB(分子量为2.4×10⁶),Hind III产生的是Hind IIIA(分子量为3.6×10⁶)和Hind IIIB(分子量为2.3×10⁶)。限制性内切酶Bam I产生四个分子量分别为2.1×10⁶(Bam IA)、2×10⁶(Bam IB)、1.25×10⁶(Bam IC)和0.24×10⁶(Bam ID)的片段,而限制性内切酶Hpa I将M-MLV双链DNA切割两次,产生三个分子量分别为4.4×10⁶(Hpa IA)、0.84×10⁶(Hpa IB)和0.74×10⁶(Hpa IC)的片段。用限制性内切酶Sma I消化M-MLV双链DNA产生四个分子量分别为3.9×10⁶(Sma IA)、1.3×10⁶(Sma IB)、0.28×10⁶(Sma IC)和0.21×10⁶(Sma ID)的片段。限制性内切酶Bgl I和Bgl II的混合物(Bgl I + II)在四个位点切割病毒DNA,产生五个近似分子量分别为2×10⁶(Bgl + IIA)、1.75×10⁶(Bgl I + IIB)、1.25×10⁶(Bgl I + IIC)、0.40×10⁶(Bgl I + IID)和0.31×10⁶(Bgl I + IIE)的片段。通过使用部分长度的M-MLV双链DNA进行限制性内切酶消化,或通过用其他限制性内切酶对Sal IA、Sal IB、Hind IIIA和Hind IIIB片段进行再消化,确定了片段相对于基因组5'端和3'端的顺序。此外,还列出了一些能切割体外合成的M-MLV双链DNA的其他限制性内切酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70e2/525888/cacbd23b81f7/jvirol00198-0094-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验