RNA processing
Roignant, JY and Soller, M. (2017). m6A in mRNA: An ancient mechanism for fine-tuning gene expression. Opinion Article. Trends in Genetics 33: 380-90.
Lence, T. Soller, M. and Roignant, JY (2017). A fly view on the roles and mechanisms of the m6A mRNA modification and its players. RNA Biology, in press
Haussmann, I.U., Bodi, Z., Sanchez-Moran, E., Mongan, N., Archer, N., Fray, R., and Soller, M. (2016) m6A potentiates Sxl alternative pre-mRNA splicing for robust Drosophila sex determination. Nature 540:301-304.
Dezi, V., Ivanov, C., Haussmann, I. U. and Soller, M. (2016) mRNA modifications and their role in development and disease. Biochem. Soc. Trans. 44: 1385-93.
Zaharieva, E., Haussmann, I. U., Brauer, U. and Soller, M. (2015) Concentration and localization of co-expressed ELAV/Hu family proteins control specificity of mRNA processing. Mol. Cell. Biol. 35: 3104-3115. Cover story
Zaharieva, E., Chipman, K, and Soller, M. (2012) Alternative splicing interference by xenobiotics. Toxicology. 296: 1-12.
Hemani, Y. and Soller, M. (2012) Mechanisms of Drosophila Dscam mutually exclusive splicing regulation. Biochem. Soc. Trans. 40: 804-9.
Haussmann, I. U., Li, M. and Soller, M. (2011). ELAV mediated 3’-end processing of ewg transcripts is evolutionary conserved despite sequence degeneration of the ELAV binding site. Genetics. 189: 97-107.
Soller, M., Li, M. and Haussmann, I.U. (2010). Determinants of ELAV gene-specific regulation. Biochem. Soc. Trans. 38: 1122-4.
Soller, M.,Li, M. and Haussmann, I.U. (2008). Regulation of the ELAV target ewg: insights from an evolutionary perspective. Biochem. Soc. Trans. 36: 502-504.
Soller, M. (2006). Pre-messengerRNA processing and its regulation: A genomic perspective. Cell. Mol. Life Sci. 63: 796-819.
Soller, M. and White, K. (2005). ELAV multimerizes on conserved AU4-6 motifs important for ewg splicing regulation. Mol. Cell. Biol. 25: 7580-7591.
Soller, M. and White, K. (2004). ELAV. Curr. Biol. 14: R53.
Soller, M. and White, K. (2003). ELAV inhibits 3' end formation to promote splicing of ewg pre-mRNA. GenesDev. 17: 2526-2538.
Neuronal development and function
Haussmann, I. U., Hemani, Y., Wjiesekera, T., Dauwalder, B. and Soller, M. (2013) Multiple pathways mediate the sex-peptide-regulated switch in female Drosophila reproductive behaviors. Proceedings of the Royal Society B 280: 20131938.
Haussmann, I.U. and Soller, M. (2010). Differential activity of EWG transcription factor isoforms identifies a subset of differentially regulated genes important for synaptic growth regulation. Dev. Biol. 348: 224-230. Cover story.
Haussmann, I. U. , White, K. and Soller, M. (2008). Erect wing regulates synaptic growth in Drosophila by integration of multiple signaling pathways. Genome Biol. 9: 73.1-17. Cover story.
Soller, M., Haussmann, I. U., Hollmann, M., Choffat, Y., White, K., Kubli, E. and Schäfer, M. A. (2006). Sex-peptide-regulated female sexual behavior requires a subset of ascending ventral nerve cord neurons. Curr. Biol. 16: 1771-1782.
Fan, Y., Soller, M., Flister, S, Hollmann, M., Müller, M., Bello, B., Egger, B., White, K., Schäfer, M. A. and Reichert, H. (2005). The egghead gene is required for compartmentalization in Drosophila optic lobe development. Dev. Biol. 287: 61-73.
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