Details

Autor(en) / Beteiligte

• Bailey, Charles G.
• Gupta, Shailendra
• Metierre, Cynthia
• Amarasekera, Punkaja M. S.
• O’Young, Patrick
• Kyaw, Wunna
• Laletin, Tatyana
• Francis, Habib
• Semaan, Crystal
• Sharifi Tabar, Mehdi
• Singh, Krishna P.
• Mullighan, Charles G.
• Wolkenhauer, Olaf
• Schmitz, Ulf
• Rasko, John E. J.

Titel

Structure–function relationships explain CTCF zinc finger mutation phenotypes in cancer

Ist Teil von

• Cellular and molecular life sciences : CMLS, 2021-12, Vol.78 (23), p.7519-7536

Ort / Verlag

Cham: Springer International Publishing

Erscheinungsjahr

2021

Link zum Volltext

Quelle

SpringerLink (Online service)

Beschreibungen/Notizen

• CCCTC-binding factor (CTCF) plays fundamental roles in transcriptional regulation and chromatin architecture maintenance. CTCF is also a tumour suppressor frequently mutated in cancer, however, the structural and functional impact of mutations have not been examined. We performed molecular and structural characterisation of five cancer-specific CTCF missense zinc finger (ZF) mutations occurring within key intra- and inter-ZF residues. Functional characterisation of CTCF ZF mutations revealed a complete (L309P, R339W, R377H) or intermediate (R339Q) abrogation as well as an enhancement (G420D) of the anti-proliferative effects of CTCF. DNA binding at select sites was disrupted and transcriptional regulatory activities abrogated. Molecular docking and molecular dynamics confirmed that mutations in residues specifically contacting DNA bases or backbone exhibited loss of DNA binding. However, R339Q and G420D were stabilised by the formation of new primary DNA bonds, contributing to gain-of-function. Our data confirm that a spectrum of loss-, change- and gain-of-function impacts on CTCF zinc fingers are observed in cell growth regulation and gene regulatory activities. Hence, diverse cellular phenotypes of mutant CTCF are clearly explained by examining structure–function relationships.