6R7O

Crystal structure of the central region of human cohesin subunit STAG1

6R7O の概要

• エントリーDOI: 10.2210/pdb6r7o/pdb
• 分子名称: Cohesin subunit SA-1 (2 entities in total)
• 機能のキーワード: cohesin, stromal antigen, chromatid, gene regulation
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 105505.88

構造登録者

Newman, J.A.,katis, V.L.,von Delft, F.,Arrowsmith, C.H.,Edwards, A.,Bountra, C.,Gileadi, O. (登録日: 2019-03-29, 公開日: 2019-04-10, 最終更新日: 2024-01-24)

主引用文献

van der Lelij, P.,Newman, J.A.,Lieb, S.,Jude, J.,Katis, V.,Hoffmann, T.,Hinterndorfer, M.,Bader, G.,Kraut, N.,Pearson, M.A.,Peters, J.M.,Zuber, J.,Gileadi, O.,Petronczki, M.
STAG1 vulnerabilities for exploiting cohesin synthetic lethality in STAG2-deficient cancers.
Life Sci Alliance, 3:-, 2020

PubMed Abstract: The cohesin subunit has emerged as a recurrently inactivated tumor suppressor in human cancers. Using candidate approaches, recent studies have revealed a synthetic lethal interaction between and its paralog To systematically probe genetic vulnerabilities in the absence of STAG2, we have performed genome-wide CRISPR screens in isogenic cell lines and identified STAG1 as the most prominent and selective dependency of STAG2-deficient cells. Using an inducible degron system, we show that chemical genetic degradation of STAG1 protein results in the loss of sister chromatid cohesion and rapid cell death in STAG2-deficient cells, while sparing -wild-type cells. Biochemical assays and X-ray crystallography identify STAG1 regions that interact with the RAD21 subunit of the cohesin complex. STAG1 mutations that abrogate this interaction selectively compromise the viability of -deficient cells. Our work highlights the degradation of STAG1 and inhibition of its interaction with RAD21 as promising therapeutic strategies. These findings lay the groundwork for the development of STAG1-directed small molecules to exploit synthetic lethality in -mutated tumors.

PubMed: 32467316
DOI: 10.26508/lsa.202000725

実験手法

X-RAY DIFFRACTION (2.31 Å)