Hamlett N V, Lange-Gufstafson B, Rhoades M
J Virol. 1977 Oct;24(1):249-60. doi: 10.1128/JVI.24.1.249-260.1977.
A physical map of the bacteriophage T5 genome was constructed by ordering the fragments produced by cleavage of T5 DNA with the restriction endonucleases SalI (4 fragments), SmaI (4 fragments), BamI (5 fragments), and HpaI (28 fragments). The following techniques were used to order the fragments. (i) Digestion of DNA from T5 heat-stable deletion mutants was used to identify fragments located in the deletable region. (ii) Fragments near the ends of the T5 DNA molecule were located by treating T5 DNA with lambda exonuclease before restriction endonuclease cleavage. (iii) Fragments spanning other restriction endonuclease cleavage sites were identified by combined digestion of T5 DNA with two restriction endonucleases. (iv) The general location of some fragments was determined by isolating individual restriction fragments from agarose gels and redigesting the isolated fragments with a second restriction enzyme. (v) Treatment of restriction digests with lambda exonuclease before digestion with a second restriction enzyme was used to identify fragments near, but not spanning, restriction cleavage sites. (vi) Exonucleases III treatment of T5 DNA before restriction endonuclease cleavage was used to locate fragments spanning or near the natural T5 single-chain interruptions. (vii) Analysis of the products of incomplete restriction endonuclease cleavage was used to identify adjacent fragments.
通过对用限制性内切酶SalI(4个片段)、SmaI(4个片段)、BamI(5个片段)和HpaI(28个片段)切割T5 DNA产生的片段进行排序,构建了噬菌体T5基因组的物理图谱。采用以下技术对片段进行排序。(i)用T5热稳定缺失突变体的DNA消化来鉴定位于可缺失区域的片段。(ii)在限制性内切酶切割之前,用λ外切核酸酶处理T5 DNA,以定位T5 DNA分子末端附近的片段。(iii)通过用两种限制性内切酶联合消化T5 DNA来鉴定跨越其他限制性内切酶切割位点的片段。(iv)通过从琼脂糖凝胶中分离单个限制性片段并用第二种限制性酶重新消化分离的片段,来确定一些片段的大致位置。(v)在用第二种限制性酶消化之前,先用λ外切核酸酶处理限制性消化产物,以鉴定靠近但不跨越限制性切割位点的片段。(vi)在限制性内切酶切割之前,用核酸外切酶III处理T5 DNA,以定位跨越或靠近天然T5单链中断处的片段。(vii)分析不完全限制性内切酶切割的产物,以鉴定相邻片段。