Nuclear Lamins: Building Blocks of Nuclear Structure and Function

Author(s):  
Robert D. Goldman ◽  
Anne E. Goldman ◽  
Dale K. Shumaker
2000 ◽  
Vol 129 (2-3) ◽  
pp. 324-334 ◽  
Author(s):  
Robert D. Moir ◽  
Timothy P. Spann ◽  
Reynold I. Lopez-Soler ◽  
Miri Yoon ◽  
Anne E. Goldman ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (17) ◽  
pp. 3074 ◽  
Author(s):  
Sofia Kolesnikova ◽  
Edward A. Curtis

G-quadruplexes are noncanonical nucleic acid structures formed from stacked guanine tetrads. They are frequently used as building blocks and functional elements in fields such as synthetic biology and also thought to play widespread biological roles. G-quadruplexes are often studied as monomers, but can also form a variety of higher-order structures. This increases the structural and functional diversity of G-quadruplexes, and recent evidence suggests that it could also be biologically important. In this review, we describe the types of multimeric topologies adopted by G-quadruplexes and highlight what is known about their sequence requirements. We also summarize the limited information available about potential biological roles of multimeric G-quadruplexes and suggest new approaches that could facilitate future studies of these structures.


Nucleus ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 90-114
Author(s):  
Matthew Goelzer ◽  
Julianna Goelzer ◽  
Matthew L. Ferguson ◽  
Corey P. Neu ◽  
Gunes Uzer

2020 ◽  
Author(s):  
Jennifer Frommer ◽  
Sabine Müller

Synthesis of site-specifically modified oligonucleotides has become a major tool for RNA structure and function studies. Reporter groups or specific functional entities are required to be attached at a pre-defined site of the oligomer.  An attractive strategy is the incorporation of suitably functionalized building blocks that allow post-synthetic conjugation of the desired moiety. A C8-alkynyl modified adenosine derivative was synthesized, reviving an old synthetic pathway for iodination of purine nucleobases. Silylation of the C8-alkynyl modified adenosine revealed unexpected selectivity of the two secondary sugar hydroxyl groups, with the 3'-O-isomer being preferentially formed. Optimization of the protection scheme lead to a new and economic route to the desired C8-alkynylated building block and its incorporation in RNA.


2011 ◽  
Vol 10 (1) ◽  
pp. 11-17 ◽  
Author(s):  
C. S. Osborne ◽  
P. A. Ewels ◽  
A. N. C. Young

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