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Increased sensitivity and accuracy of a single-stranded DNA splint-mediated ligation assay (sPAT) reveals poly(A) tail length dynamics of developmentally regulated mRNAs

机译:单链DNA夹板介导的连接测定(sPAT)的灵敏度和准确性提高揭示了发育受调控的mRNA的poly(A)尾长动态

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摘要

Poly(A) tail length is a readout of an mRNA’s translatability and stability, especially in developmental systems. PolyAdenylation Test (PAT) assays attempt to quickly measure the average poly(A) tail length of RNAs of experimental interest. Here we present sPAT, splint-mediated PAT, a procedure that uses a DNA splint to aid in the ligation of an RNA-tag to the poly(A) tail of an mRNA. In comparison to other PAT methodologies, including ePAT, sPAT is highly sensitive to low-abundance mRNAs, gives a more accurate profile of the poly(A) tail distribution, and requires little starting material. To demonstrate its strength, we calibrated sPAT on defined poly(A) tails of synthetic mRNAs, reassessed developmentally regulated poly(A) tail-length changes of known mRNAs from established model organisms, and extended it to the emerging evolutionary developmental nematode model Pristionchus pacificus. Lastly, we used sPAT to analyze the contribution of the two cytoplasmic poly(A) polymerases GLD-2 and GLD-4, and the deadenylase CCR-4, onto Caenorhabditis elegans gld-1 mRNA that encodes a translationally controlled tumor suppressor whose poly(A) tail length measurement proved elusive.
机译:Poly(A)尾巴长度是mRNA的可翻译性和稳定性的读数,尤其是在发育系统中。聚腺苷酸化测试(PAT)分析试图快速测量实验性RNA的平均poly(A)尾部长度。在这里,我们介绍了sPAT,夹板介导的PAT,该程序使用DNA夹板来帮助将RNA标签连接到mRNA的poly(A)尾巴。与包括ePAT在内的其他PAT方法相比,sPAT对低丰度mRNA高度敏感,可更准确地分析poly(A)尾巴分布,并且所需原料很少。为了证明其强度,我们在合成的mRNA定义的poly(A)尾部上校准了sPAT,重新评估了已建立的模型生物中已知mRNA的发育调控的poly(A)尾部长度变化,并将其扩展到了新兴的进化发育线虫模型Pristionchus pacificus 。最后,我们使用sPAT分析了两种胞质多聚(A)聚合酶GLD-2和GLD-4,以及腺苷酸酶CCR-4对秀丽隐杆线虫gld-1 mRNA的贡献,该编码编码受翻译控制的肿瘤抑制因子, A)尾巴长度测量证明难以捉摸。

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