Shih C K, Linial M, Goodenow M M, Hayward W S
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4697-701. doi: 10.1073/pnas.81.15.4697.
We have determined the nucleotide sequence of the 2.2-kilobase-pair region upstream of the chicken c-myc coding exons. Using RNA blot analysis, we have localized a noncoding exon to a region that is separated from the c-myc coding sequences by an intron of 700-800 base pairs. In most avian leukosis virus-induced lymphomas proviral integration has occurred within, or downstream of, the first exon, thus presumably displacing the regulatory sequences that normally control c-myc expression. More than 70% of the integration sites were clustered in a 250-base-pair region in the first intron, immediately preceding the coding sequences. Sequences from the upstream noncoding exon were absent from the myc transcripts in these lymphomas; RNA transcripts from the normal c-myc allele were not expressed at detectable levels.
我们已经确定了鸡c-myc编码外显子上游2.2千碱基对区域的核苷酸序列。通过RNA印迹分析,我们将一个非编码外显子定位到了一个区域,该区域与c-myc编码序列之间被一个700 - 800个碱基对的内含子隔开。在大多数禽白血病病毒诱导的淋巴瘤中,前病毒整合发生在第一个外显子内部或下游,因此可能取代了正常控制c-myc表达的调控序列。超过70%的整合位点聚集在第一个内含子中紧接编码序列之前的一个250个碱基对的区域。在这些淋巴瘤的myc转录本中没有上游非编码外显子的序列;正常c-myc等位基因的RNA转录本未检测到表达。