Pochart P, Agoutin B, Rousset S, Chanet R, Doroszkiewicz V, Heyman T
Institut Curie-Biologie, URA 1342 CNRS, Orsay, France.
Nucleic Acids Res. 1993 Jul 25;21(15):3513-20. doi: 10.1093/nar/21.15.3513.
Transposition of Saccharomyces cerevisiae Ty1 retroelements has been shown to involve reverse transcription in intracytoplasmic virus-like particles (Ty-VLPs). Ty DNA present in the particles specified by Ty1-H3 element was found to consist of the full-length genomic DNA as well as incomplete cDNAs mainly of plus polarity. Our results indicate that identical sequences (TGGGTGGTA) are used as primers for the synthesis of plus strand cDNA, generating cDNAs of 0.345 kb (analogous to the retroviral strong-stop plus cDNA) and of 2.1 kb. Electron microscopic analyses of Ty1-VLP DNA revealed two distinct classes, one full-length and the other corresponding to 0.34 kbp molecules, the size of a LTR sequence. The full-length molecules are either completely double-stranded or only partially double- stranded at one end or at both ends. These double-stranded regions are of a length corresponding to those of incomplete plus strands detected by biochemical techniques. Double-stranded circular molecules mainly of a length corresponding to that of two-LTR circles were also detected on electron micrographs. These analyses allowed us to propose a scheme for reverse transcription in Ty particles.
酿酒酵母Ty1逆转录元件的转座已被证明涉及在胞质内病毒样颗粒(Ty-VLPs)中的逆转录过程。由Ty1-H3元件指定的颗粒中存在的Ty DNA被发现由全长基因组DNA以及主要为正链极性的不完整cDNA组成。我们的结果表明,相同序列(TGGGTGGTA)被用作合成正链cDNA的引物,产生0.345 kb(类似于逆转录病毒强终止正链cDNA)和2.1 kb的cDNA。对Ty1-VLP DNA的电子显微镜分析揭示了两种不同类型,一种是全长的,另一种对应于0.34 kbp的分子,即LTR序列的大小。全长分子要么完全是双链的,要么在一端或两端只是部分双链的。这些双链区域的长度与通过生化技术检测到的不完整正链的长度相对应。在电子显微镜照片上还检测到主要长度对应于两个LTR环的双链环状分子。这些分析使我们能够提出Ty颗粒中逆转录的方案。