# p31Comet Splice Variants Induce Distinct Spindle Assembly Checkpoint Dynamics due to Their Unique N-Termini

**Authors:** Luke Scarberry, Garrett Thesing, Kevin Brennan, Madison Williams, Matthew K. Summers

PMC · DOI: 10.3390/ijms26073089 · International Journal of Molecular Sciences · 2025-03-27

## TL;DR

Two versions of a protein called p31Comet behave differently in cell division, with one version being less effective and more unstable, especially in the testes.

## Contribution

The study reveals that the N-terminal region of p31Comet splice variants affects their function in mitosis and stability.

## Key findings

- Variant 1 of p31Comet has reduced binding to MAD2 and slower mitotic progression compared to Variant 2.
- Variant 1 is less stable than Variant 2 and is uniquely expressed in the testes.
- The N-terminus of p31Comet modulates its activity during mitosis.

## Abstract

The role of p31Comet in deactivating the spindle assembly checkpoint is well described in the literature; however, the data are all completed using Variant 2 of p31Comet. p31Comet is known to be expressed as two different splice variants: Variant 1 and Variant 2. Variant 1 contains an additional 32 N-terminal residues compared to Variant 2. We report that Variant 1 exhibits a reduced ability to bind to MAD2 and thus a reduced ability to induce mitotic progression. Additionally, we show that Variant 1 exhibits reduced stability compared to Variant 2. We further show that Variant 1 is uniquely expressed in the Testes, indicating a potentially unique role of Variant 1 in that organ. Overall, we demonstrate the N-terminus of p31Comet is capable of modulating p31Comet activity in mitosis.

## Linked entities

- **Genes:** MAD2L1BP (MAD2L1 binding protein) [NCBI Gene 9587]
- **Proteins:** MAD2L1BP (MAD2L1 binding protein), MAD2L1 (mitotic arrest deficient 2 like 1)

## Full-text entities

- **Genes:** MAD2L1 (mitotic arrest deficient 2 like 1) [NCBI Gene 4085] {aka HSMAD2, MAD2}

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11989133/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC11989133/full.md

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Source: https://tomesphere.com/paper/PMC11989133