Ghysdael J, Hubert E, Trávnícek M, Bolognesi D P, Burny A, Cleuter Y, Huez G, Kettmann R, Marbaix G, Portetelle D, Chantrenne H
Proc Natl Acad Sci U S A. 1977 Aug;74(8):3230-4. doi: 10.1073/pnas.74.8.3230.
After microinjection of Xenopus laevis oocytes with RNA from avian myeloblastosis virus, viral structural proteins p27, p19, p15, and p12 are formed by a sequence of posttranslational cleavages of a high-molecular-weight precursor polypeptide. The 60-70S RNA aggregate or its 30-40S RNA subunits obtained by heat or formamide treatment possess the same ability to serve as template in X. laevis oocytes. The processing pattern of virus-specific precursor polypeptides is the same in X. laevis oocytes as in chick embryo fibroblasts infected with avian myeloblastosis virus, but the processing takes place at a much slower rate.
用禽成髓细胞瘤病毒的RNA显微注射非洲爪蟾卵母细胞后,病毒结构蛋白p27、p19、p15和p12是由一种高分子量前体多肽经一系列翻译后切割形成的。通过加热或甲酰胺处理获得的60 - 70S RNA聚集体或其30 - 40S RNA亚基在非洲爪蟾卵母细胞中具有相同的作为模板的能力。病毒特异性前体多肽的加工模式在非洲爪蟾卵母细胞中与感染禽成髓细胞瘤病毒的鸡胚成纤维细胞中相同,但加工速度要慢得多。