Nascent RNA signaling to yeast RNA Pol II during transcription elongation

Transcription as the key step in gene expression is a highly regulated process. The speed of transcription elongation depends on the underlying gene sequence and varies on a gene by gene basis. The reason for this sequence dependence is not known in detail. Recently, our group studied the cross talk between the nascent RNA and the transcribing RNA polymerase by screening the Escherichia coli genome for RNA sequences with high affinity to RNA Pol by performing genomic SELEX. This approach led to the identification of RNA polymerase-binding APtamers termed “ RAPs”. RAPscan have positive and negative effects on gene expression. A subgroup is able to downregulate transcription via the activity of the termination factorRho. In this study, we used a similar SELEX setup using yeast genomic DNA as source of RNA sequences and highly purified yeast RNA Pol II as bait and obtained almost 1300 yeast-derived RAPs. Yeast RAPsare found throughout the genome within genes and antisense to genes, they are overrepresented in the non-transcribed strand of yeast telomeres and underrepresented in intergenic regions. Genes harbouring a RAPare more likely to show lower mRNA levels. By determining the endogenous expression levels as well as using a reporter system, we show that RAPslocated within coding regions can reduce the transcript level downstream of the RAP. Here we demonstrate that RAPsrepresent a novel type of regulatory RNA signal in Saccharomyces cerevisiae that act in cis and interfere with the elongating transcription machinery to reduce the transcriptional output.