Ohtake Y, Wickner R B
Section of Genetics of Simple Eukaryotes, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892, USA.
Mol Cell Biol. 1995 May;15(5):2772-81. doi: 10.1128/MCB.15.5.2772.
Over 30 MAK (maintenance of killer) genes are necessary for propagation of the killer toxin-encoding M1 satellite double-stranded RNA of the L-A virus. Sequence analysis revealed that MAK7 is RPL4A, one of the two genes encoding ribosomal protein L4 of the 60S subunit. We further found that mutants with mutations in 18 MAK genes (including mak1 [top1], mak7 [rpl4A], mak8 [rpl3], mak11, and mak16) had decreased free 60S subunits. Mutants with another three mak mutations had half-mer polysomes, indicative of poor association of 60S and 40S subunits. The rest of the mak mutants, including the mak3 (N-acetyltransferase) mutant, showed a normal profile. The free 60S subunits, L-A copy number, and the amount of L-A coat protein in the mak1, mak7, mak11, and mak16 mutants were raised to the normal level by the respective normal single-copy gene. Our data suggest that most mak mutations affect M1 propagation by their effects on the supply of proteins from the L-A virus and that the translation of the non-poly(A) L-A mRNA depends critically on the amount of free 60S ribosomal subunits, probably because 60S association with the 40S subunit waiting at the initiator AUG is facilitated by the 3' poly(A).
超过30个MAK(杀伤维持)基因对于L-A病毒的杀伤毒素编码M1卫星双链RNA的繁殖是必需的。序列分析表明,MAK7是RPL4A,即编码60S亚基核糖体蛋白L4的两个基因之一。我们进一步发现,18个MAK基因(包括mak1[top1]、mak7[rpl4A]、mak8[rpl3]、mak11和mak16)发生突变的突变体,其游离60S亚基减少。另外三个mak突变的突变体具有半聚核糖体,表明60S和40S亚基的结合较差。其余的mak突变体,包括mak3(N-乙酰转移酶)突变体,表现出正常的分布。通过各自的正常单拷贝基因,mak1、mak7、mak11和mak16突变体中的游离60S亚基、L-A拷贝数和L-A衣壳蛋白量提高到正常水平。我们的数据表明,大多数mak突变通过影响L-A病毒蛋白质的供应来影响M1的繁殖,并且非聚腺苷酸L-A mRNA的翻译关键取决于游离60S核糖体亚基的数量,这可能是因为3'聚腺苷酸促进了60S与在起始AUG处等待的40S亚基的结合。