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. 2019 Nov 20;8:e50496. doi: 10.7554/eLife.50496

Figure 2. Y2H assays reveal domains involved in homo/heterodimerization.

(A) Yeast two-hybrid assays between the three Zasp paralogs. Images of double-transformed yeast grown in selective -Ade/-His/-Leu/-Trp plates. Serial dilutions are shown from left to right (OD: 0.1, OD: 0.01, and OD: 0.001). Zasp52-PK dimerizes with itself and with the longer isoform Zasp52-PE. Zasp66 interacts with Zasp52-PK and Zasp52-PE. Zasp67 interacts with Zasp52-PK and Zasp52-PE. Negative controls using the DNA-binding domain (bait, pGAD-T7) or the Activating domain of Gal4 (prey, pGBK-T7) are shown. (B) Y2H assays testing the interaction between all protein domains encoded by the Zasp52 gene and Zasp52-PK, Zasp66-PK, or Zasp67-PD proteins. Zasp52-PK interacts with isolated ZM and LIM domains, Zasp66-PK and Zasp67-PD interact only with some LIM domains. LIM1A, LIM1B, LIM2A, and LIM2B are different splice isoforms of LIM1 and LIM2 domains. (C) Proposed model of Zasp homo/heterodimerization. The LIM domains bind the ZM domain. Zasp52-PK dimerization occurs through two ZM/LIM pairs. The heterodimerization between Zasp52-PK and Zasp66-PK or Zasp67-PD occurs through only one ZM/LIM-binding site. Zasp66-PH is a small isoform that only contains a ZM domain. (D) Y2H assays mapping the interaction between different Zasp52 LIM domains to Zasp66-PK using truncation mutants. (E) Y2H assays testing the interaction between the ZM only isoform Zasp66-PH, and the individual protein domains encoded by Zasp52.

Figure 2.

Figure 2—figure supplement 1. Zasp self-interaction by co-IP and chemical crosslinking.

Figure 2—figure supplement 1.

(A) Endogenous Zasp52 tagged with GFP was purified from thorax extracts via GFP beads. GFP-Zasp52 co-immunoprecipitates Flag-Zasp52-PK. GFP alone was used as negative control. (B) Purified His-Zasp52-PK-Flag from bacteria was treated with the chemical crosslinker ethylene glycol bis-sulfosuccinimidyl succinate (EGS) and then analyzed by SDS-Page. In addition to monomers (M, 50 kD), dimers (D) are observed upon EGS treatment.