SPP1935 Logo

SPP1935 -- Deciphering the mRNP code :
RNA-bound Determinants of Post-transcriptional Gene Regulation

LoginLogin New userNew User LoginShare

laboratoriesDr. Landthaler

Markus Landthaler Center
Berlin Institute for Medical Systems Biology
Max Delbrück Center for Molecular Medicine in the

Robert-Rössle-Straße 10 13125 Berlin, Germany


Send an Email

Online Website

Understanding the molecular interactions and mechanisms of the RNA helicase DDX6 in posttranscriptional regulation


RNA fate determination is at the center of gene expression regulation, influencing the stability, localization, and translation efficiency of mRNAs. Here, we propose to characterize the RNA helicase DDX6 and its role in posttranscriptional regulation. DDX6 is known to be involved in mRNA localization and storage in different protein-mRNA granules, recruitment of mRNA degradation enzymes, and translational repression. Despite its importance the RNA-target specificity and the detailed molecular functions of DDX6 remain elusive.

We will deliver three major milestones that are independent from each other, but feed into a system-wide description of DXX6’s specificity and regulation at the example of human HEK293 cells. We will map the mRNA interactome of DDX6 and mutant variants using protein-RNA crosslinking, immunoprecipitation, and next-generation sequencing to identify mRNAs where DDX6 binds, the region within the mRNA, and how the repertoire of putative targets changes. We will characterize the repertoire of protein interaction partners and DDX6-protein complexes through proximity biotinylation followed by mass spectrometry. To characterize the global molecular impact of DDX6 function, we will deplete the helicase and determine changes in mRNA half-lives and ribosome occupancy. These three assays provide an overview of the changes that putative target transcripts may undergo with respect to their mRNA stability and translation.

None of these proposed studies has been performed before in a comprehensive, system-wide manner, and their combination will provide synergistic information on changes in the functions and molecular targets of DDX6, depending on its interactions with other putative regulators. As RNA-binding proteins are still systematically understudied, we will provide important insights of the roles of a key player in post-transcriptional regulation of gene expression.

Focus of the group :
Regulatory functions of RNA-binding proteins


- mRNA Interactome capture

PublicationsPUBLICATIONS :

Wessels HH, Imami K, Baltz AG, Kolinski M, Beldovskaya A, Selbach M, Small S, Ohler U#, Landthaler M#. (2016) The mRNA-bound proteome of the early fly embryo.
Genome Res. 2016 Apr 28.

Murakawa Y, Hinz M, Mothes J, Schuetz A, Uhl M, Wyler E, Yasuda T, Mastrobuoni G, Friedel CC, Dölken L, Kempa S, Schmidt-Supprian M, Blüthgen N, Backofen R, Heinemann U, Wolf J, Scheidereit C, Landthaler M. (2015) RC3H1 post-transcriptionally regulates A20 mRNA and modulates the activity of the IKK/NF-κB pathway.
Nature Communications 6:7367

Rybak-Wolf A, Jens M, Murakawa Y, Herzog M, Landthaler M#, Rajewsky N#. (2014) A variety of Dicer substrates in human and C.elegans.
Cell 159:1153-1167.

Gregersen LH, Schueler M, Munschauer M, Mastrobuoni G, Chen W, Kempa S, Dieterich C, Landthaler M. (2014) MOV10 is a 5’ to 3’ RNA helicase contributing to UPF1 mRNA target degradation by translocation along 3’UTRs.
Molecular Cell 54: 573-585.

Baltz AG, Munschauer M, Schwanhausser B, Vasile A, Murakawa Y, Schueler M, Youngs N, Penfold-Brown D, Drew K, Milek M, Wyler E, Bonneau R, Selbach M, Dieterich C, and Landthaler, M (2012) The mRNA-Bound Proteome and Its Global Occupancy Profile on Protein-Coding Transcripts.
Molecular Cell 46, 674-90.