PT  - JOURNAL ARTICLE
AU  - Joseph M. Varberg
AU  - Jennifer M. Gardner
AU  - Scott McCroskey
AU  - Snehabala Saravanan
AU  - William D. Bradford
AU  - Sue L. Jaspersen
TI  - High-throughput identification of nuclear envelope protein interactions in <em>Schizosaccharomyces pombe</em> using an arrayed membrane yeast-two hybrid library
AID  - 10.1101/2020.07.29.227819
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.07.29.227819
4099  - http://biorxiv.org/content/early/2020/07/30/2020.07.29.227819.short
4100  - http://biorxiv.org/content/early/2020/07/30/2020.07.29.227819.full
AB  - The nuclear envelope (NE) contains a specialized set of integral membrane proteins that maintain nuclear shape and integrity and influence chromatin organization and gene expression. Advances in proteomics techniques and studies in model organisms have identified hundreds of proteins that localize to the NE. However, the function of many of these proteins at the NE remains unclear, in part due to a lack of understanding of the interactions that these proteins participate in at the NE membrane. To assist in the characterization of NE transmembrane protein interactions we developed an arrayed library of integral and peripheral membrane proteins in the fission yeast Schizosaccharomyces pombe for high-throughput screening using the split-ubiquitin based membrane yeast two hybrid sys-tem. We used this approach to characterize protein interactions for three conserved proteins that localize to the inner nu-clear membrane: Cut11/Ndc1, Lem2, and Ima1/Samp1/NET5. Additionally, we determined how the interaction network for Cut11 is altered in canonical temperature-sensitive cut11 mutants. This library and screening approach is readily applicable to characterizing the interactomes of integral membrane proteins localizing to various subcellular compartments.Competing Interest StatementThe authors have declared no competing interest.