Nuclear speckle proteins form intrinsic and MALAT1-dependent microphases

Shinn, M. K.; Tomares, D. T.; Liu, V.; Pant, A.; Qiu, Y.; Song, Y. J.; Ayala, Y. M.; Strout, G. W.; Ruff, K. M.; Lew, M. D.; Prasanth, K. V.; Pappu, R. V.

doi:10.1101/2025.02.26.640430

bioRxiv · 10.1101/2025.02.26.640430

Nuclear speckle proteins form intrinsic and MALAT1-dependent microphases

Shinn, M. K.·Tomares, D. T.·Liu, V.·Pant, A.·Qiu, Y.·Song, Y. J.·Ayala, Y. M.·Strout, G. W.·Ruff, K. M.·Lew, M. D.·Prasanth, K. V.·Pappu, R. V.

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Abstract

Nuclear speckles are enriched in serine / arginine rich splicing factors (SRSFs), such as SRSF1. Splicing factors and proteins such as TDP-43 concentrate into distinct speckle territories to enable pre-mRNA processing. We have discovered that SRSFs and TDP-43 are block copolymers and the protein-specific interplay of inter-block repulsions and attractions drives spontaneous microphase separation. This gives rise to size-limited, ordered assemblies, that are 30 - 45 nm in diameter. Depending on the protein, each microphase comprises several tens to hundreds of molecules. The sub-micron scale territories observed in cells are shown to be clusters of microphases. The regulatory lncRNA MALAT1 binds preferentially to SRSF1 microphases to enhance microphase separation and alter microphase structures. Microphase separation enables the concentration of finite numbers of splicing factors into assemblies with distinct nanoscale structures that can be modulated by MALAT1. Our findings provide a structural framework for the functional organization of splicing factors.

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Shinn, M. K., Tomares, D. T., Liu, V., Pant, A., Qiu, Y., Song, Y. J., Ayala, Y. M., Strout, G. W., Ruff, K. M., Lew, M. D., Prasanth, K. V., Pappu, R. V.. 2025-02-27. Nuclear speckle proteins form intrinsic and MALAT1-dependent microphases. https://doi.org/10.1101/2025.02.26.640430

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