Bridging the gap between in vitro and in vivo RNA folding. (24th June 2016)
- Record Type:
- Journal Article
- Title:
- Bridging the gap between in vitro and in vivo RNA folding. (24th June 2016)
- Main Title:
- Bridging the gap between in vitro and in vivo RNA folding
- Authors:
- Leamy, Kathleen A.
Assmann, Sarah M.
Mathews, David H.
Bevilacqua, Philip C. - Abstract:
- Abstract: Deciphering the folding pathways and predicting the structures of complex three-dimensional biomolecules is central to elucidating biological function. RNA is single-stranded, which gives it the freedom to fold into complex secondary and tertiary structures. These structures endow RNA with the ability to perform complex chemistries and functions ranging from enzymatic activity to gene regulation. Given that RNA is involved in many essential cellular processes, it is critical to understand how it folds and functions in vivo . Within the last few years, methods have been developed to probe RNA structures in vivo and genome-wide. These studies reveal that RNA often adopts very different structures in vivo and in vitro, and provide profound insights into RNA biology. Nonetheless, both in vitro and in vivo approaches have limitations: studies in the complex and uncontrolled cellular environment make it difficult to obtain insight into RNA folding pathways and thermodynamics, and studies in vitro often lack direct cellular relevance, leaving a gap in our knowledge of RNA folding in vivo . This gap is being bridged by biophysical and mechanistic studies of RNA structure and function under conditions that mimic the cellular environment. To date, most artificial cytoplasms have used various polymers as molecular crowding agents and a series of small molecules as cosolutes. Studies under such in vivo-like conditions are yielding fresh insights, such as cooperative folding ofAbstract: Deciphering the folding pathways and predicting the structures of complex three-dimensional biomolecules is central to elucidating biological function. RNA is single-stranded, which gives it the freedom to fold into complex secondary and tertiary structures. These structures endow RNA with the ability to perform complex chemistries and functions ranging from enzymatic activity to gene regulation. Given that RNA is involved in many essential cellular processes, it is critical to understand how it folds and functions in vivo . Within the last few years, methods have been developed to probe RNA structures in vivo and genome-wide. These studies reveal that RNA often adopts very different structures in vivo and in vitro, and provide profound insights into RNA biology. Nonetheless, both in vitro and in vivo approaches have limitations: studies in the complex and uncontrolled cellular environment make it difficult to obtain insight into RNA folding pathways and thermodynamics, and studies in vitro often lack direct cellular relevance, leaving a gap in our knowledge of RNA folding in vivo . This gap is being bridged by biophysical and mechanistic studies of RNA structure and function under conditions that mimic the cellular environment. To date, most artificial cytoplasms have used various polymers as molecular crowding agents and a series of small molecules as cosolutes. Studies under such in vivo-like conditions are yielding fresh insights, such as cooperative folding of functional RNAs and increased activity of ribozymes. These observations are accounted for in part by molecular crowding effects and interactions with other molecules. In this review, we report milestones in RNA folding in vitro and in vivo and discuss ongoing experimental and computational efforts to bridge the gap between these two conditions in order to understand how RNA folds in the cell. … (more)
- Is Part Of:
- Quarterly reviews of biophysics. Volume 49(2016)
- Journal:
- Quarterly reviews of biophysics
- Issue:
- Volume 49(2016)
- Issue Display:
- Volume 49, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 49
- Issue:
- 2016
- Issue Sort Value:
- 2016-0049-2016-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-06-24
- Subjects:
- Biophysics -- Periodicals
571.405 - Journal URLs:
- http://journals.cambridge.org/action/displayJournal?jid=QRB ↗
- DOI:
- 10.1017/S003358351600007X ↗
- Languages:
- English
- ISSNs:
- 0033-5835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 5738.xml