van der Kuyl A C, Neeleman L, Bol J F
Gorlaeus Laboratories, Leiden University, The Netherlands.
Virology. 1991 Aug;183(2):731-8. doi: 10.1016/0042-6822(91)91002-x.
Deletions were made in an infectious cDNA clone of alfalfa mosaic virus (AIMV) RNA3 and the replication of RNA transcripts of these cDNAs was studied in tobacco plants transformed with AIMV replicase genes (P12 plants). Previously, we found that deletions in the P3 gene did not affect accumulation of RNA3 in P12 protoplasts whereas deletions in the coat protein (CP) gene reduced accumulation 100-fold (A. C. van der Kuyl, L. Neeleman, and J. F. Bol, 1991, Virology 183, 687-694). In P12 plants deletions in the P3 gene reduced accumulation by about 200-fold and accumulation of CP deletion mutants was not detectable. When P12 plants were inoculated with a mixture of P3- and CP-deletion mutants, both mutants replicated efficiently and various amounts of full-length RNA3 molecules were formed by recombination. The observation that some P3 and CP mutants did not recombine at a detectable level after several passages in P12 plants demonstrated that mutations in the AIMV P3 and CP genes can be complemented in trans.
对苜蓿花叶病毒(AIMV)RNA3的感染性cDNA克隆进行了缺失突变,并在转AIMV复制酶基因的烟草植株(P12植株)中研究了这些cDNA的RNA转录本的复制情况。此前,我们发现P3基因的缺失不影响RNA3在P12原生质体中的积累,而外壳蛋白(CP)基因的缺失则使积累量降低了100倍(A.C.范德·奎尔、L.内勒曼和J.F.博尔,1991年,《病毒学》183卷,687 - 694页)。在P12植株中,P3基因的缺失使积累量降低了约200倍,而CP缺失突变体的积累量则无法检测到。当用P3和CP缺失突变体的混合物接种P12植株时,两种突变体都能高效复制,并且通过重组形成了各种数量的全长RNA3分子。在P12植株中传代几次后,一些P3和CP突变体未在可检测水平上发生重组,这一观察结果表明AIMV P3和CP基因中的突变可以通过反式互补。