Recent insights into the mechanisms controlling gene expression identified enhancer-associated long non-coding RNAs (elncRNAs) as master players of transcription in cancers. RUNX2, a mammalian RUNT-related transcription factor, is increasingly recognized in cancer biology for its role in supporting survival and progression also in thyroid cancer (TC). We recently identified, within the RUNX2 locus, a novel elncRNA that we named RAIN (RUNX2 associated intergenic lncRNA). We showed that RAIN and RUNX2 expression correlate in TC, both in vitro and in vivo, and that RAIN promotes RUNX2 expression by interacting with and affecting the activity of the RUNX2 P2 promoter through two distinct mechanisms. Here, we took forward these observations to explore the genome-wide transcriptional function of RAIN and its contribution to the RUNX2-dependent gene expression program in TC. By combining multiple omics data, we demonstrated that RAIN functionally cooperates with RUNX2 to the regulation of a subset of functionally related genes involved in promoting matrix remodeling, migration, and loss of differentiation. We showed that RAIN interacts with RUNX2 and its expression is required for the efficient recruitment of this TF to its target regulatory regions. In addition, our data revealed that besides RUNX2, RAIN governs a hierarchically organized complex transcriptional program by controlling a core of cancer-associated TFs that, in turn, orchestrate the expression of downstream genes. This evidence indicates that the functional cooperation observed between RAIN and RUNX2 can be a diffuse work mechanism for this elncRNA.

Exploring the transcriptional cooperation between RUNX2 and its associated elncRNA RAIN / Vitale, E.; Manicardi, V.; Gugnoni, M.; Torricelli, F.; Donati, B.; Muccioli, S.; Salviato, E.; Rossi, T.; Manzotti, G.; Piana, S.; Ciarrocchi, A.. - In: CELL DEATH & DISEASE. - ISSN 2041-4889. - 15:9(2024), pp. 1-13. [10.1038/s41419-024-07058-x]

Exploring the transcriptional cooperation between RUNX2 and its associated elncRNA RAIN

Vitale E.;Manicardi V.;Torricelli F.;Manzotti G.;
2024

Abstract

Recent insights into the mechanisms controlling gene expression identified enhancer-associated long non-coding RNAs (elncRNAs) as master players of transcription in cancers. RUNX2, a mammalian RUNT-related transcription factor, is increasingly recognized in cancer biology for its role in supporting survival and progression also in thyroid cancer (TC). We recently identified, within the RUNX2 locus, a novel elncRNA that we named RAIN (RUNX2 associated intergenic lncRNA). We showed that RAIN and RUNX2 expression correlate in TC, both in vitro and in vivo, and that RAIN promotes RUNX2 expression by interacting with and affecting the activity of the RUNX2 P2 promoter through two distinct mechanisms. Here, we took forward these observations to explore the genome-wide transcriptional function of RAIN and its contribution to the RUNX2-dependent gene expression program in TC. By combining multiple omics data, we demonstrated that RAIN functionally cooperates with RUNX2 to the regulation of a subset of functionally related genes involved in promoting matrix remodeling, migration, and loss of differentiation. We showed that RAIN interacts with RUNX2 and its expression is required for the efficient recruitment of this TF to its target regulatory regions. In addition, our data revealed that besides RUNX2, RAIN governs a hierarchically organized complex transcriptional program by controlling a core of cancer-associated TFs that, in turn, orchestrate the expression of downstream genes. This evidence indicates that the functional cooperation observed between RAIN and RUNX2 can be a diffuse work mechanism for this elncRNA.
2024
15
9
1
13
Exploring the transcriptional cooperation between RUNX2 and its associated elncRNA RAIN / Vitale, E.; Manicardi, V.; Gugnoni, M.; Torricelli, F.; Donati, B.; Muccioli, S.; Salviato, E.; Rossi, T.; Manzotti, G.; Piana, S.; Ciarrocchi, A.. - In: CELL DEATH & DISEASE. - ISSN 2041-4889. - 15:9(2024), pp. 1-13. [10.1038/s41419-024-07058-x]
Vitale, E.; Manicardi, V.; Gugnoni, M.; Torricelli, F.; Donati, B.; Muccioli, S.; Salviato, E.; Rossi, T.; Manzotti, G.; Piana, S.; Ciarrocchi, A....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1363527
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