TWIST1 and chromatin regulatory proteins interact to guide neural crest cell differentiation
| Autor: | V. Pragathi Masamsetti, Patrick P.L. Tam, Kasper Engholm-Keller, Pierre Osteil, Xiaochen Fan, Mark E. Graham, Nicolas Fossat, Joshua Studdert, Jane Q. J. Sun |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Nervous system
animal structures Mouse QH301-705.5 Ectomesenchyme Science Biology General Biochemistry Genetics and Molecular Biology Mice 03 medical and health sciences neural stem cell 0302 clinical medicine proteomics Specialization (functional) medicine Animals Biology (General) Embryonic Stem Cells 030304 developmental biology 0303 health sciences General Immunology and Microbiology neurodevelopment General Neuroscience Twist-Related Protein 1 Neural crest Cell Differentiation Cell Biology General Medicine neurocristopathy ectomesenchyme craniofacial development Chromatin Neural stem cell Neural crest cell differentiation medicine.anatomical_structure Neural Crest embryonic structures Medicine Developmental biology Neuroscience 030217 neurology & neurosurgery Research Article Developmental Biology |
| Zdroj: | eLife, Vol 10 (2021) eLife |
| Popis: | Protein interaction is critical molecular regulatory activity underlining cellular functions and precise cell fate choices. Using TWIST1 BioID-proximity-labeling and network propagation analyses, we discovered and characterized a TWIST-chromatin regulatory module (TWIST1-CRM) in the neural crest cells (NCC). Combinatorial perturbation of core members of TWIST1-CRM: TWIST1, CHD7, CHD8, and WHSC1 in cell models and mouse embryos revealed that loss of the function of the regulatory module resulted in abnormal differentiation of NCCs and compromised craniofacial tissue patterning. Following NCC delamination, low level of TWIST1-CRM activity is instrumental to stabilize the early NCC signatures and migratory potential by repressing the neural stem cell programs. High level of TWIST1 module activity at later phases commits the cells to the ectomesenchyme. Our study further revealed the functional interdependency of TWIST1 and potential neurocristopathy factors in NCC development. eLife digest Shaping the head and face during development relies on a complex ballet of molecular signals that orchestrates the movement and specialization of various groups of cells. In animals with a backbone for example, neural crest cells (NCCs for short) can march long distances from the developing spine to become some of the tissues that form the skull and cartilage but also the pigment cells and nervous system. NCCs mature into specific cell types thanks to a complex array of factors which trigger a precise sequence of binary fate decisions at the right time and place. Amongst these factors, the protein TWIST1 can set up a cascade of genetic events that control how NCCs will ultimately form tissues in the head. To do so, the TWIST1 protein interacts with many other molecular actors, many of which are still unknown. To find some of these partners, Fan et al. studied TWIST1 in the NCCs of mice and cells grown in the lab. The experiments showed that TWIST1 interacted with CHD7, CHD8 and WHSC1, three proteins that help to switch genes on and off, and which contribute to NCCs moving across the head during development. Further work by Fan et al. then revealed that together, these molecular actors are critical for NCCs to form cells that will form facial bones and cartilage, as opposed to becoming neurons. This result helps to show that there is a trade-off between NCCs forming the face or being part of the nervous system. One in three babies born with a birth defect shows anomalies of the head and face: understanding the exact mechanisms by which NCCs contribute to these structures may help to better predict risks for parents, or to develop new approaches for treatment. |
| Databáze: | OpenAIRE |
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