Eichinger D J, Boeke J D
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Cell. 1988 Sep 23;54(7):955-66. doi: 10.1016/0092-8674(88)90110-9.
Yeast Ty1 elements are retrotransposons that transpose via an RNA intermediate found in a virus-like particle (Ty-VLP). A Ty-encoded reverse transcriptase activity found inside the particles is capable of giving rise to full-length reverse transcripts. The predominant form of these reverse transcripts is a full-length linear duplex DNA. We have developed a cell-free system for transposition of Ty1 DNA molecules into a bacteriophage lambda target. Purified Ty-VLPs and target DNA are the only macromolecular components required for the transposition reaction. A TYB-encoded protein, p90-TYB, contains amino acid sequences that are similar to those of retroviral integrase proteins. Mutations in the integrase coding region abolish transposition both in vivo and in vitro.
酵母Ty1元件是逆转座子,通过存在于病毒样颗粒(Ty-VLP)中的RNA中间体进行转座。在颗粒内部发现的一种由Ty编码的逆转录酶活性能够产生全长逆转录产物。这些逆转录产物的主要形式是全长线性双链DNA。我们已经开发了一种无细胞系统,用于将Ty1 DNA分子转座到噬菌体λ靶标中。纯化的Ty-VLP和靶标DNA是转座反应所需的仅有的大分子成分。一种由TYB编码的蛋白质p90-TYB,其氨基酸序列与逆转录病毒整合酶蛋白的序列相似。整合酶编码区的突变在体内和体外均消除转座。