مورد إلكتروني

Beyond tethering and the LEM domain: MSCellaneous functions of the inner nuclear membrane Lem2

التفاصيل البيبلوغرافية
العنوان: Beyond tethering and the LEM domain: MSCellaneous functions of the inner nuclear membrane Lem2
بيانات النشر: Taylor & Francis 2016
تفاصيل مُضافة: Friedrich-Baur-Institute (Germany)
German Research Foundation
Braun, Sigurd
Barrales, Ramón R.
نوع الوثيقة: Electronic Resource
مستخلص: The nuclear envelope plays a pivotal role in the functional organization of chromatin. Various inner nuclear membrane (INM) proteins associate with transcriptionally repressed chromatin, which is often found at the nuclear periphery. A prominent example is the conserved family of LEM (LAP2-Emerin-MAN1) domain proteins that interact with DNA-binding proteins and have been proposed to mediate tethering of chromatin to the nuclear membrane. We recently reported that the fission yeast protein Lem2, a homolog of metazoan LEM proteins, contributes to perinuclear localization and silencing of heterochromatin. We demonstrate that binding and tethering of centromeric chromatin depends on the LEM domain of Lem2. Unexpectedly, this domain is dispensable for heterochromatin silencing, which is instead mediated by a different structural domain of Lem2, the MSC (MAN1-Src1 C-terminal) domain. Hence, silencing and tethering by Lem2 can be mechanistically separated. Notably, the MSC domain has multiple functions beyond heterochromatic silencing. Here we discuss the implications of these novel findings for the understanding of this conserved INM protein.
مصطلحات الفهرس: LEM domain, Perinuclear silencing, Heterochromatin, Chromatin tethering, MSC domain, artículo
URL: http://hdl.handle.net/10261/163188
Sí
info:eu-repo/grantAgreement/EC/FP7/257082
الإتاحة: Open access content. Open access content
closedAccess
ملاحظة: English
أرقام أخرى: CTK oai:digital.csic.es:10261/163188
Nucleus 7(6): 523-531 (2016)
10.1080/19491034.2016.1252892
27797637
1105215759
المصدر المساهم: CSIC
From OAIster®, provided by the OCLC Cooperative.
رقم الأكسشن: edsoai.on1105215759
قاعدة البيانات: OAIster