Max Planck Institute for Multidisciplinary Sciences, Department of Physical Biochemistry, 37077 Göttingen, Germany.
Nucleic Acids Res. 2024 Jun 24;52(11):6507-6517. doi: 10.1093/nar/gkae396.
The ribosome can slide along mRNA without establishing codon-anticodon interactions. This movement can be regulated (programmed) by the elements encoded in the mRNA, as observed in bypassing of non-coding gap in gene 60 of bacteriophage T4, or occur spontaneously, such as during traversal by the 70S ribosome of the 3'UTRs or upon re-initiation on bacterial polycistronic genes. In this study, we investigate the kinetic mechanism underlying the programmed and spontaneous ribosome sliding. We show that the translation rate of gene 60 mRNA decreases as the ribosome approaches the take-off site, especially when the KKYK regulatory sequence in the nascent peptide reaches the constriction site in the ribosome exit tunnel. However, efficiency of bypassing increases when the ribosome traverses the gap quickly. With the non-coding gap exceeding the natural 50 nt, the processivity of sliding remains high up to 56 nt, but drops sharply beyond that due to the loss of mRNA elements support. Sliding efficiency is temperature-dependent; while temperature regulates the number of ribosomes initiating programmed bypassing, traversing the long gaps becomes increasingly unfavorable at lower temperatures. This data offers novel insights into the kinetic determinants of programmed and spontaneous ribosome sliding along the mRNA.
核糖体可以在不建立密码子-反密码子相互作用的情况下沿 mRNA 滑动。这种运动可以通过 mRNA 中编码的元件进行调节(编程),如在噬菌体 T4 基因 60 的非编码缺口绕过中观察到的那样,或者自发发生,例如在 70S 核糖体穿越 3'UTR 或在细菌多顺反子基因上重新起始时。在这项研究中,我们研究了编程和自发核糖体滑动的动力学机制。我们表明,当核糖体接近起飞位点时,基因 60 mRNA 的翻译速率会降低,特别是当新生肽中的 KKYK 调节序列到达核糖体出口隧道中的收缩位点时。然而,当核糖体快速穿越缺口时,旁路的效率会增加。当非编码缺口超过自然的 50nt 时,滑动的连续性仍然高达 56nt,但超过该值后由于 mRNA 元件支持的丢失而急剧下降。滑动效率与温度有关;虽然温度调节了启动编程旁路的核糖体数量,但在较低温度下,穿越长缺口变得越来越不利。这些数据为编程和自发核糖体沿 mRNA 滑动的动力学决定因素提供了新的见解。