دورية أكاديمية

The lncRNAs at X Chromosome Inactivation Center: Not Just a Matter of Sex Dosage Compensation

التفاصيل البيبلوغرافية
العنوان: The lncRNAs at X Chromosome Inactivation Center: Not Just a Matter of Sex Dosage Compensation
المؤلفون: Chiara Siniscalchi, Armando Di Palo, Aniello Russo, Nicoletta Potenza
المصدر: International Journal of Molecular Sciences, Vol 23, Iss 2, p 611 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: ceRNET, microRNA, lncRNA, X chromosome inactivation, Turner syndrome, Klinefelter syndrome, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: Non-coding RNAs (ncRNAs) constitute the majority of the transcriptome, as the result of pervasive transcription of the mammalian genome. Different RNA species, such as lncRNAs, miRNAs, circRNA, mRNAs, engage in regulatory networks based on their reciprocal interactions, often in a competitive manner, in a way denominated “competing endogenous RNA (ceRNA) networks” (“ceRNET”): miRNAs and other ncRNAs modulate each other, since miRNAs can regulate the expression of lncRNAs, which in turn regulate miRNAs, titrating their availability and thus competing with the binding to other RNA targets. The unbalancing of any network component can derail the entire regulatory circuit acting as a driving force for human diseases, thus assigning “new” functions to “old” molecules. This is the case of XIST, the lncRNA characterized in the early 1990s and well known as the essential molecule for X chromosome inactivation in mammalian females, thus preventing an imbalance of X-linked gene expression between females and males. Currently, literature concerning XIST biology is becoming dominated by miRNA associations and they are also gaining prominence for other lncRNAs produced by the X-inactivation center. This review discusses the available literature to explore possible novel functions related to ceRNA activity of lncRNAs produced by the X-inactivation center, beyond their role in dosage compensation, with prospective implications for emerging gender-biased functions and pathological mechanisms.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1422-0067
1661-6596
Relation: https://www.mdpi.com/1422-0067/23/2/611; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms23020611
URL الوصول: https://doaj.org/article/dfb4def861334bdf80d7af3c97746f18
رقم الأكسشن: edsdoj.fb4def861334bdf80d7af3c97746f18
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14220067
16616596
DOI:10.3390/ijms23020611