This document summarizes research finding that Smad proteins, which are transcription factors activated by TGF-β and BMP signaling, directly bind to a conserved RNA sequence called CAGAC to promote the processing of specific microRNAs by the Drosha complex. The study found that CAGAC sequences are required for Smad-mediated processing of miR-21 and other microRNAs. Smad proteins directly associate with pri-miRNAs containing CAGAC sequences to facilitate their cleavage by Drosha into pre-miRNAs. This reveals a mechanism by which TGF-β/BMP signaling can rapidly modulate microRNA expression at the post-transcriptional level in response to cellular stimuli.
Genetic retargeting of E3 ligases to enhance CAR T therapy
Keystone Symposia 2010
1. Smad Proteins Bind a Conserved RNA Sequence to Promote microRNA Maturation by Drosha Brandi N. Davis, PhD Tufts Medical Center Mentor: Akiko Hata, PhD
10. The CAGAC sequence is required for Smad-mediated miRNA processing Pri-miR-21 WT loop 5’ m1 m2 m3
11. Insertion of the CAGAC sequence can confer Smad-mediated miRNA processing C. Elegans miR-84 WT C. Elegans miR-84 5’ C. Elegans miR-84 3’ C. Elegans miR-84 mid miR-21 WT WT 5’ 3’ WT mid C. Elegans miR-84 miR-21
First mention that both BMP and TGF-b do this, and that this is the first instance of post-transcriptional regulation of microRNAs due to extracellular signal Also inducate that thus, TGF-B and BMP can regulate gene expression through two ways, one is through transcription and the second is through post-transcriptional regulation of microRNA expression , say that TGF-B signaling promotes the association of the Smads with pri-miRNAs which promotes their processing by drosha, onced processed the pre miRNA is transported out of the nucleus where it undergoes dicer processing to generate the mature miRNA which can alter gene expression post transcriptionally
The fold induction of miRNA expression was then clustered. Because miR-21 was similarly induced by both BMP4 and TGF-b we chose the cluster of miRNAs induced by both growth factors this group included miR-21. We hypothesized that smad-regulated miRNAs may share a defining feature which allows them to be regulated. In order to begin to think about the mechanism, I need to tell you a bit more details about the general structure of pri-miRNAs. We compared the sequence and predicted structures of the cluster one miRNAs using motif detection programs. Interestingly this analysis identified a motif which was centrally located in the mature miRNA, and composed of the sequence CAGAC. Given that this is the same sequence which smad optimally binds in DNA, we thought that this sequence could be important for the selection of miRNAs for post-transcriptional processing. Thus we used a sequence motif finding program to identify over-represented sequences present in the cluster 1 miRNAs. Interestingly, the consensus motif CAGAC was identified in the mature miRNA.
Remember to say fold induction by BMPEmphasize that m3 maintains the secondary structure of the hairpin.
When correctly positioned, the CAGAC sequence can provide Smad mediated processing.