Academic Journal

The spliceosome inhibitors isoginkgetin and pladienolide B induce ATF3-dependent cell death.

التفاصيل البيبلوغرافية
العنوان: The spliceosome inhibitors isoginkgetin and pladienolide B induce ATF3-dependent cell death.
المؤلفون: Erin J Vanzyl, Hadil Sayed, Alex B Blackmore, Kayleigh R C Rick, Pasan Fernando, Bruce C McKay
المصدر: PLoS ONE, Vol 15, Iss 12, p e0224953 (2020)
بيانات النشر: Public Library of Science (PLoS)
سنة النشر: 2020
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Medicine, Science
الوصف: The spliceosome assembles on pre-mRNA in a stepwise manner through five successive pre-spliceosome complexes. The spliceosome functions to remove introns from pre-mRNAs to generate mature mRNAs that encode functional proteins. Many small molecule inhibitors of the spliceosome have been identified and they are cytotoxic. However, little is known about genetic determinants of cell sensitivity. Activating transcription factor 3 (ATF3) is a transcription factor that can stimulate apoptotic cell death in response to a variety of cellular stresses. Here, we used a genetic approach to determine if ATF3 was important in determining the sensitivity of mouse embryonic fibroblasts (MEFs) to two splicing inhibitors: pladienolide B (PB) and isoginkgetin (IGG), that target different pre-spliceosome complexes. Both compounds led to increased ATF3 expression and apoptosis in control MEFs while ATF3 null cells were significantly protected from the cytotoxic effects of these drugs. Similarly, ATF3 was induced in response to IGG and PB in the two human tumour cell lines tested while knockdown of ATF3 protected cells from both drugs. Taken together, ATF3 appears to contribute to the cytotoxicity elicited by these spliceosome inhibitors in both murine and human cells.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1932-6203
Relation: https://doi.org/10.1371/journal.pone.0224953; https://doaj.org/toc/1932-6203; https://doaj.org/article/90ec183a8f8c474faf2968abd8490439
DOI: 10.1371/journal.pone.0224953
الاتاحة: https://doi.org/10.1371/journal.pone.0224953
https://doaj.org/article/90ec183a8f8c474faf2968abd8490439
رقم الانضمام: edsbas.C53175AC
قاعدة البيانات: BASE
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0224953