Nuclear localization and transactivation of SYS-1/β-catenin is the result of serial gene duplications and subfunctionalizations
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Updated: Jun 14, 2025

Heterokaryon Technique for Analysis of Cell Type-specific Localization
Published on: March 11, 2011
Arielle K Wolf1, Lori C Adams-Phillips1, Amanda N D Adams1
1University of Iowa, Iowa, IA, United States of America.
Abstract:
β-catenin is a highly conserved multifunctional protein capable of mediating cell adhesion via E-cadherin and transactivation of target genes of the canonical Wnt signaling pathway. The nematode, C. elegans contains four paralogs of β-catenin which are highly specific in their functions. Though similar in overall structure, the four beta-catenins are functionally distinct, each regulating different aspects of development. Of the four, SYS-1 is a key player in Wnt dependent asymmetric cell division (ACD). In ACD, a polarized mother will give rise to a daughter with high nuclear SYS-1 and another with low nuclear SYS-1. Despite sequence dissimilarity, SYS-1 shares a close structural resemblance with human β-catenin where it retains an unstructured amino-terminus (NTD) and 12 armadillo repeats. Using existing genome sequence data from several nematode species, we find that the four β-catenin paralogs result from 3 sequential gene duplications and neofunctionalizations during nematode evolution. SYS-1, however, lacks an unstructured carboxyl-terminus (CTD) that is essential for human β-catenin transactivation processes. This work supports the hypothesis that SYS-1 compensated for the lack of CTD by acquiring novel transactivation domains with cryptic nuclear localization signals in the NTD and the first four armadillo repeats, as shown by transactivation assays in worms and yeast. Furthermore, SYS-1 regulatory domains are not localized to the NTD as in canonical β-catenin and instead spans the entire length of the protein. Truncating SYS-1 abolishes the classical SYS-1 nuclear asymmetry, resulting in daughter cells with symmetrical SYS-1 truncation localization. A screen for SYS-1 physical interactors followed by in vivo SYS-1 localization analyses and effects on cell fate suggest that proper SYS-1 nuclear export is facilitated by XPO-1, while an interaction with IMB-3, an importin β-like protein, suggests import mechanisms. Interestingly, XPO-1 is especially required for lowering SYS-1 in the Wnt-unsignaled nucleus, suggesting a distinct mechanism for regulating asymmetric nuclear SYS-1. In summary, we provide insights on the mechanism of β-catenin evolution within nematodes and inform SYS-1 transactivation and nuclear transport mechanisms.
Insights
The evolution of C. elegans SYS-1 beta-catenin involved gene duplications and novel domain acquisition for Wnt signaling and asymmetric cell division. Nuclear transport mechanisms, including XPO-1 and IMB-3, regulate SYS-1 localization for proper cell fate determination.
Area of Science:
- Evolutionary developmental biology
- Molecular cell biology
- Genetics
Background:
- Beta-catenin proteins are crucial for cell adhesion and Wnt signaling.
- C. elegans possesses four distinct beta-catenin paralogs, including SYS-1, vital for development.
- SYS-1 plays a key role in Wnt-dependent asymmetric cell division (ACD).
Purpose of the Study:
- To investigate the evolutionary origins of C. elegans beta-catenin paralogs.
- To elucidate the mechanisms of SYS-1 transactivation and nuclear transport.
- To understand how SYS-1 compensates for structural differences compared to human beta-catenin.
Main Methods:
- Comparative genomics to trace beta-catenin gene evolution.
- Transactivation assays in C. elegans and yeast to study SYS-1 function.
- Interaction screens and localization studies to identify SYS-1 transport factors.
Main Results:
- The four C. elegans beta-catenin paralogs arose from three gene duplications and neofunctionalizations.
- SYS-1 lacks the typical human beta-catenin carboxyl-terminal domain but compensates with novel transactivation domains.
- SYS-1's regulatory domains span the entire protein length, and its nuclear transport involves XPO-1 and IMB-3.
Conclusions:
- SYS-1 evolved unique mechanisms for transactivation and nuclear localization, distinct from canonical beta-catenin.
- XPO-1 and IMB-3 facilitate SYS-1 nuclear import and export, with XPO-1 specifically regulating Wnt-unsignaled nuclear SYS-1 levels.
- This study provides insights into beta-catenin evolution and the regulation of asymmetric cell division in nematodes.
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