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Approaches to probe and perturb long noncoding RNA functions in diseases.
Wang, Guiping; Lee-Yow, Yannick; Chang, Howard Y.
Afiliación
  • Wang G; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA 94305, USA. Electronic address: https://twitter.com/@Guiping_W.
  • Lee-Yow Y; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA 94305, USA. Electronic address: https://twitter.com/@yooaaooy.
  • Chang HY; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA 94305, USA. Electronic address: howchang@stanford.edu.
Curr Opin Genet Dev ; 85: 102158, 2024 04.
Article en En | MEDLINE | ID: mdl-38412563
ABSTRACT
Long noncoding RNAs (lncRNAs) are a class of RNA molecules exceeding 200 nucleotides in length that lack long open-reading frames. Transcribed predominantly by RNA polymerase II (>500nt), lncRNAs can undergo splicing and are produced from various regions of the genome, including intergenic regions, introns, and in antisense orientation to protein-coding genes. Aberrations in lncRNA expression or function have been associated with a wide variety of diseases, including cancer, cardiovascular diseases, diabetes, and neurodegeneration. Despite the growing recognition of select lncRNAs as key players in cellular processes and diseases, several challenges obscure a comprehensive understanding of their functional landscape. Recent technological innovations, such as in sequencing, affinity-based techniques, imaging, and RNA perturbation, have advanced functional characterization and mechanistic understanding of disease-associated lncRNAs.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / ARN Largo no Codificante Límite: Humans Idioma: En Revista: Curr Opin Genet Dev Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / ARN Largo no Codificante Límite: Humans Idioma: En Revista: Curr Opin Genet Dev Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article