共 69 条
Challenges in the analysis of long noncoding RNA functionality
被引:39
作者:

Leone, Sergio
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Zurich, Dept Mol Mech Dis, CH-8057 Zurich, Switzerland
Univ Zurich, Mol Life Sci Program, Life Sci Zurich Grad Sch, Zurich, Switzerland Univ Zurich, Dept Mol Mech Dis, CH-8057 Zurich, Switzerland

Santoro, Raffaella
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h-index: 0
机构:
Univ Zurich, Dept Mol Mech Dis, CH-8057 Zurich, Switzerland Univ Zurich, Dept Mol Mech Dis, CH-8057 Zurich, Switzerland
机构:
[1] Univ Zurich, Dept Mol Mech Dis, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Mol Life Sci Program, Life Sci Zurich Grad Sch, Zurich, Switzerland
基金:
瑞士国家科学基金会;
关键词:
chromatin;
epigenetics;
genome organization;
lncRNA;
triple helix;
REMODELING COMPLEX NORC;
INACTIVE X-CHROMOSOME;
ACID TRIPLE-HELICES;
XIST RNA;
HETEROCHROMATIN FORMATION;
DOSAGE COMPENSATION;
MSL COMPLEX;
MOLECULAR-MECHANISMS;
IN-VIVO;
CHROMATIN;
D O I:
10.1002/1873-3468.12308
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Long noncoding RNA (lncRNA) are emerging as important regulators of diverse biological functions. Although mechanistic models are starting to emerge, it is also clear that the lncRNA field needs appropriate model systems in order to better elucidate the functions of lncRNA and their roles in both physiological and pathological conditions. The field of lncRNA is new, and the biochemical and genetic methods used to address function and mechanisms of lncRNA have only recently been developed or adapted from techniques used to investigate protein-coding genes. In this review, we discuss the strengths and weaknesses of available techniques for the analysis of chromatin-associated lncRNA and emerging models for the recruitment to specific genomic sites such as triple-helix, RNA-protein-DNA recognition and proximity-guided search models.
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页码:2342 / 2353
页数:12
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