Author

R. Pantier

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Cell Biology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:mouse· 3 Research Focus:chromatin & epigenetic regulation· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:development & morphogenesis· 1 Assay:DNA methylation· 1 Organism:human· 1

Frequent Co-Authors

E. Hall-Ponsele· 2 shared I. Chambers· 2 shared N. Mullin· 2 shared A. Bird· 1 shared A. Corsinotti· 1 shared A. G. Cook· 1 shared A. P. Bird· 1 shared B. Alexander-Howden· 1 shared

Activity by Year

2017-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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2 shared papersBiochemistry

E. Hall-Ponsele

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Author profile →

4 papers

Recent·Most cited

MeCP2 binds to methylated DNA independently of phase separation and heterochromatin organisation

R. Pantier, M. Brown, S. Han, K. Paton, S. Meek, T. Montavon, T. McHugh, D. A. Kelly, T. Hochepied, C. Libert, T. Jenuwein, T. Burdon, A. Bird

This paper shows MeCP2 binds methylated DNA without needing phase separation or heterochromatin, and its foci are rare in most mammals.

bioRxiv · May 9, 2023Cell Biology

Structural analysis of SALL4 zinc-finger domain reveals a link between AT-rich DNA binding and Okihiro syndrome

J. A. Watson, R. Pantier, U. Jayachandran, K. Chhatbar, B. Alexander-Howden, V. Kruusvee, M. Prendecki, A. P. Bird, A. G. Cook

This study presents the crystal structure of SALL4 zinc fingers bound to AT-rich DNA, showing flexible recognition and links to Okihiro syndrome mutations.

bioRxiv · Jun 14, 2022Biochemistry

TET1 interacts directly with NANOG via independent regions containing hydrophobic and aromatic residues

R. Pantier, N. Mullin, E. Hall-Ponsele, I. Chambers

This study identifies the regions of TET1 that interact with NANOG, showing that these interactions are mediated by conserved hydrophobic and aromatic residues and occur at pluripotency enhancers.

bioRxiv · Jun 29, 2020Biochemistry

Distinct SoxB1 networks are required for naïve and primed pluripotency

A. Corsinotti, F. C. Wong, T. Tatar, I. Szczerbinska, F. Halbritter, D. Colby, S. Gogolok, R. Pantier, K. Liggat, E. S. Mirfazeli, E. Hall-Ponsele, N. Mullin, V. Wilson, I. Chambers

The paper shows that distinct SoxB1 networks support naïve and primed pluripotency, with different expression balances of Sox2 and Sox3 in ESCs and EpiSCs.

bioRxiv · Dec 6, 2017Cell Biology