Dina D
Proc Natl Acad Sci U S A. 1978 Jun;75(6):2694-8. doi: 10.1073/pnas.75.6.2694.
Labeled, purified 30S RNA from Moloney murine sarcoma virus was annealed to an excess of Moloney murine leukemia virus complementary DNA. Upon treatment of the resulting DNA.RNA hybrids with RNase H followed by sucrose gradient sedimentation, and undigested 18S RNA molecule was recovered. This RNA molecule was shown to represent the "sarcoma-specific" region of the virus. The unintegrated linear DNA provirus of murine sarcoma virus 124 was isolated from newly infected cells and a physical map of the sarcoma-specific region was obtained. First, unintegrated full-length linear proviral DNA molecules were cleaved by several restriction endonucleases. The reciprocal position and orientation with respect to the viral RNA of the resulting fragments were established. The location of the sarcoma-specific region was determined by competition-hybridization with 125I-labeled viral genomic RNAs and proviral DNA fragments. A 1500-base-pair fragment was obtained by cleavage with HindIII + Bgl II. This fragment mapped between 750 and 2250 base pairs from the right end of the proviral DNA (corresponding th the 3' terminus of the viral RNA) and contained the whole set of the sarcoma-specific information. This murine sarcoma virus proviral restriction fragment is approximately of the same size and map position as the isolated 18S sarcoma-specific RNA.
将来自莫洛尼氏鼠肉瘤病毒的经标记和纯化的30S RNA与过量的莫洛尼氏鼠白血病病毒互补DNA进行退火处理。用核糖核酸酶H处理所得的DNA-RNA杂交体,随后进行蔗糖梯度沉降,回收未消化的18S RNA分子。该RNA分子被证明代表病毒的“肉瘤特异性”区域。从新感染的细胞中分离出鼠肉瘤病毒124的未整合线性DNA前病毒,并获得了肉瘤特异性区域的物理图谱。首先,用几种限制性内切酶切割未整合的全长线性前病毒DNA分子。确定了所得片段相对于病毒RNA的相互位置和方向。通过与125I标记的病毒基因组RNA和前病毒DNA片段进行竞争杂交来确定肉瘤特异性区域的位置。用HindIII + Bgl II切割得到一个1500个碱基对的片段。该片段位于前病毒DNA右端750至2250个碱基对之间(对应于病毒RNA的3'末端),并包含整套肉瘤特异性信息。这个鼠肉瘤病毒前病毒限制性片段的大小和图谱位置与分离出的18S肉瘤特异性RNA大致相同。