Chiang Chiayn, Chen Guang-Wu, Shih Shin-Ru
Research Center for Emerging Viral Infections, Chang Gung University, Kwei-Shan, Taoyuan, Taiwan.
J Virol. 2008 Nov;82(21):10873-86. doi: 10.1128/JVI.00506-08. Epub 2008 Sep 3.
Different amino acid sequences of influenza virus proteins contribute to different viral phenotypes. However, the diversity of the sequences and its impact on noncoding regions or splice sites have not been intensively studied. This study focuses on the sequences at alternative 5' splice sites on M1 mRNA. Six different mutations at the splice sites were introduced, and viral growth characteristics for those mutants generated by reverse genetics with 12 plasmids were examined, for which G12C (the G-to-C mutation at the first nucleotide of the intron for the mRNA3 5' splice site), C51G (at the 3' end of the exon of the M2 mRNA 5' splice site), and G146C (for the first nucleotide of the intron for mRNA4) are lethal mutations. On the other hand, mutants with the mutation G11C (at the 3' end of exon of the mRNA3 5' splice site), G52C (for the first nucleotide of the intron for M2 mRNA), or G145A (at the 3' end of the exon of mRNA4) were rescued, although they had significantly attenuated growth rates. Notably, these mutations did not change any amino acids in M1 or M2 proteins. The levels of precursor (M1 mRNA) and spliced products (M2 mRNA, mRNA3, and mRNA4) from the recombinant mutant virus-infected cells were further analyzed. The production levels of mRNA3 in cells infected with G11C, G52C, and G145A mutant viruses were reduced in comparison with that in wild-type recombinant virus-infected ones. More M2 mRNA was produced in G11C mutant virus-infected cells than in wild-type-virus-infected cells, and there was little M2 mRNA and none at all in G145A and G52C mutant virus-infected ones, respectively. Results obtained here suggest that introducing these mutations into the alternative 5' splice sites disturbed M1 mRNA splicing, which may attenuate viral growth rates.
流感病毒蛋白的不同氨基酸序列导致不同的病毒表型。然而,序列的多样性及其对非编码区或剪接位点的影响尚未得到深入研究。本研究聚焦于M1 mRNA上可变5'剪接位点的序列。在剪接位点引入了六种不同的突变,并检测了通过12个质粒的反向遗传学产生的那些突变体的病毒生长特性,其中G12C(mRNA3 5'剪接位点内含子第一个核苷酸处的G到C突变)、C51G(M2 mRNA 5'剪接位点外显子的3'端)和G146C(mRNA4内含子的第一个核苷酸)是致死突变。另一方面,具有G11C(mRNA3 5'剪接位点外显子的3'端)、G52C(M2 mRNA内含子的第一个核苷酸)或G145A(mRNA4外显子的3'端)突变的突变体被拯救出来,尽管它们的生长速率显著降低。值得注意的是,这些突变并未改变M1或M2蛋白中的任何氨基酸。进一步分析了重组突变病毒感染细胞中前体(M1 mRNA)和剪接产物(M2 mRNA、mRNA3和mRNA4)的水平。与野生型重组病毒感染的细胞相比,感染G11C、G52C和G145A突变病毒的细胞中mRNA3的产生水平降低。G11C突变病毒感染的细胞中产生的M2 mRNA比野生型病毒感染的细胞中更多,但G145A和G52C突变病毒感染的细胞中分别几乎没有M2 mRNA和完全没有M2 mRNA。此处获得的结果表明,将这些突变引入可变5'剪接位点会干扰M1 mRNA剪接,这可能会降低病毒生长速率。