In this project, we have been asking two main questions. First, we wanted to determine if ZNHIT6 could be a new SUMO E3 ligase. By employing rigours biochemical tests, we demonstrated that despite being a very good SUMOylation substrate, ZNHIT6 is not a SUMO ligase. The second question was aimed at understanding the role of ZNHIT6 in regulation of RNA metabolism. For this, we have managed to characterize the expression and localization of ZNHIT6 as well as the consequences of its constitutive knock-out, which provides us with some information about its biological role. In addition, we have performed a number of interesting experiments, through which we wanted to assess the role of ZNHIT6 and SUMO in the regulation of a biologically crucial process of stem cell differentiation. As such, we have generated a unique dataset that is completely novel in the stem cell field.
I will aim to publish all my research data in open-access journals as soon as possible. I have also decided to deposit all my proteomics data sets in PRIDE repository managed by EBI, which I believe will be a valuable resource for the research community as we have created unique and novel data sets that could give rise to interesting projects in the future. So far, I have presented my data as a poster during 2017 EMBO Conference on Ubiquitin and SUMO: From molecular mechanisms to systemwide responses in Cavtat in Croatia and during our yearly Department meetings. A paper describing the SUMO proteome of human iPS cells and how it changes during differentiation is in preparation. “Dramatic changes to the SUMO proteome during differentiation of human induced pluripotent stem cells”
See Figure 1. Schematic representation of the progress of the project incorporating research questions and obtained results [Figure 1 is attached to the Summary for Publication].