4.5 Article

Impact of poly(A)-tail G-content on Arabidopsis PAB binding and their role in enhancing translational efficiency

期刊

GENOME BIOLOGY
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-019-1799-8

关键词

Poly(A) tails; Poly(A)-binding proteins; PAB binding efficiency; Poly(A)-tail G-content; mRNA stability; Translational efficiency; Arabidopsis

资金

  1. National Natural Science Foundation of China [31788103, 91540203, 31770874, 31900455, 31571308, 31701096]
  2. National Basic Research Program of China [2014CB943400]
  3. Strategic Priority Research Program of Chinese Academy of Sciences [XDPB0403, XDB27030201, XDA08020303]
  4. Key Research Program of Frontier Sciences of Chinese Academy of Sciences [QYZDY-SSW-SMC022]
  5. State Key Laboratory of Plant Genomics

向作者/读者索取更多资源

Background Polyadenylation plays a key role in producing mature mRNAs in eukaryotes. It is widely believed that the poly(A)-binding proteins (PABs) uniformly bind to poly(A)-tailed mRNAs, regulating their stability and translational efficiency. Results We observe that the homozygous triple mutant of broadly expressed Arabidopsis thaliana PABs, AtPAB2, AtPAB4, and AtPAB8, is embryonic lethal. To understand the molecular basis, we characterize the RNA-binding landscape of these PABs. The AtPAB-binding efficiency varies over one order of magnitude among genes. To identify the sequences accounting for the variation, we perform poly(A)-seq that directly sequences the full-length poly(A) tails. More than 10% of poly(A) tails contain at least one guanosine (G); among them, the G-content varies from 0.8 to 28%. These guanosines frequently divide poly(A) tails into interspersed A-tracts and therefore cause the variation in the AtPAB-binding efficiency among genes. Ribo-seq and genome-wide RNA stability assays show that AtPAB-binding efficiency of a gene is positively correlated with translational efficiency rather than mRNA stability. Consistently, genes with stronger AtPAB binding exhibit a greater reduction in translational efficiency when AtPAB is depleted. Conclusions Our study provides a new mechanism that translational efficiency of a gene can be regulated through the G-content-dependent PAB binding, paving the way for a better understanding of poly(A) tail-associated regulation of gene expression.

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