Sanson B, Uzan M
CNRS URA1139, Institut de Biologie Physico-chimique, Paris, France.
FEMS Microbiol Rev. 1995 Aug;17(1-2):141-50. doi: 10.1111/j.1574-6976.1995.tb00196.x.
Gene regB of bacteriophage T4 encodes a sequence-specific endoribonuclease which introduces cuts in early phage messenger RNAs. In most cases, cutting takes place in the middle of the tetranucleotide GGAG. Efficient cleavages occur in the motifs located in intergenic regions, some of them being Shine-Dalgarno sequences. When located in a coding sequence, this tetranucleotide is poorly recognized or not at all. In this article, we have reviewed the properties of the RegB endoribonuclease, with emphasis on its possible roles in T4 development. We show that the nuclease RegB plays at least two roles: (i) it inactivates a sub-class of early mRNA by cleaving Shine-Dalgarno sequences, and (ii) it is necessary for the degradation of early mRNAs, but not of middle and late mRNAs. Accordingly, we found that middle and late mRNAs avoid processing by RegB, probably for different reasons. Most of the middle mRNAs (mRNAs initiated at MotA-dependent promoters) do not contain the motif GGAG in their intergenic regions, whereas about one-third of the late genes have this motif as Shine-Dalgarno sequence. It is not yet known whether the RNase is inactivated early in the phage cycle, or whether it remains active but cannot recognize late mRNAs as substrates.
噬菌体T4的基因regB编码一种序列特异性核糖核酸内切酶,该酶可在早期噬菌体信使核糖核酸(mRNA)上进行切割。在大多数情况下,切割发生在四核苷酸GGAG的中间。高效切割发生在基因间隔区的基序中,其中一些是Shine-Dalgarno序列。当位于编码序列中时,这个四核苷酸很难被识别或根本不被识别。在本文中,我们综述了RegB核糖核酸内切酶的特性,重点讨论了其在T4噬菌体发育中可能发挥的作用。我们发现该核酸酶RegB至少发挥两个作用:(i)通过切割Shine-Dalgarno序列使一类早期mRNA失活;(ii)它是早期mRNA降解所必需的,但不是中期和晚期mRNA降解所必需的。因此,我们发现中期和晚期mRNA可能由于不同原因而避免被RegB加工。大多数中期mRNA(从依赖MotA的启动子起始的mRNA)在其基因间隔区不包含基序GGAG,而约三分之一的晚期基因具有该基序作为Shine-Dalgarno序列。目前尚不清楚该核糖核酸酶是在噬菌体周期早期失活,还是仍然具有活性但不能将晚期mRNA识别为底物。