The emergence of Sox and POU transcription factors predates the origins of animal stem cells

Ya Gao, Daisylyn Senna Tan, Mathias Girbig, Haoqing Hu, Xiaomin Zhou, Qianwen Xie, Shi Wing Yeung, Kin Shing Lee, Sik Yin Ho, Vlad Cojocaru, Jian Yan, Georg K. A. Hochberg, Alex de Mendoza, Ralf Jauch

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Stem cells are a hallmark of animal multicellularity. Sox and POU transcription factors are associated with stemness and were believed to be animal innovations, reported absent in their unicellular relatives. Here we describe unicellular Sox and POU factors. Choanoflagellate and filasterean Sox proteins have DNA-binding specificity similar to mammalian Sox2. Choanoflagellate—but not filasterean—Sox can replace Sox2 to reprogram mouse somatic cells into induced pluripotent stem cells (iPSCs) through interacting with the mouse POU member Oct4. In contrast, choanoflagellate POU has a distinct DNA-binding profile and cannot generate iPSCs. Ancestrally reconstructed Sox proteins indicate that iPSC formation capacity is pervasive among resurrected sequences, thus loss of Sox2-like properties fostered Sox family subfunctionalization. Our findings imply that the evolution of animal stem cells might have involved the exaptation of a pre-existing set of transcription factors, where pre-animal Sox was biochemically similar to extant Sox, whilst POU factors required evolutionary innovations. © The Author(s) 2024.
Original languageEnglish
Article number9868
JournalNature Communications
Volume15
Online published14 Nov 2024
DOIs
Publication statusPublished - 2024

Funding

This work used computing resources from Queen Mary University of London’s Apocrita HPC facilities by A.d.M. General Research Fund (RGC/GRF, Grant. No. 17117823, 17101120 and 17106622 to R.J.). Research Grants Council of Hong Kong Collaborative Research Fund (RGC/CRF, Grant No. C7064-22G to R.J.). Health and Medical Research Fund (08192886 to R.J.). Innovation Technology Commission Funding Scheme Health@InnoHK. European Research Council Starting Grant (950230 to A.d.M.). M.G. acknowledges support by the Peter und Traudl Engelhorn Foundation. G.K.A.H. is supported by the Max-Planck Society.

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  • This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/

RGC Funding Information

  • RGC-funded

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