Specific synonymous mutations tightly correlate with HIV-1 co-receptor usage and differentially affect the secondary structure of HIV-1 Env RNA

2021 ◽  
Vol 65 (02) ◽  
pp. 173-180
Author(s):  
Salvatore Dimonte ◽  
Lavinia Fabeni ◽  
Michele Pellegrino ◽  
Stefano Aquaro
AIDS ◽  
2000 ◽  
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pp. 1721-1729 ◽  
Author(s):  
Lucia Ometto ◽  
Marisa Zanchetta ◽  
Monica Mainardi ◽  
Gian Luca De Salvo ◽  
Marie Cruz Garcia-Rodriguez ◽  
...  

2010 ◽  
Vol 203 (2) ◽  
pp. 237-245 ◽  
Author(s):  
L. C. Swenson ◽  
T. Mo ◽  
W. W. Y. Dong ◽  
X. Zhong ◽  
C. K. Woods ◽  
...  

Open Biology ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 190020 ◽  
Author(s):  
Daniel Gebert ◽  
Julia Jehn ◽  
David Rosenkranz

Codon composition, GC content and local RNA secondary structures can have a profound effect on gene expression, and mutations affecting these parameters, even though they do not alter the protein sequence, are not neutral in terms of selection. Although evidence exists that, in some cases, selection favours more stable RNA secondary structures, we currently lack a concrete idea of how many genes are affected within a species, and whether this is a universal phenomenon in nature. We searched for signs of structural selection in a global manner, analysing a set of 1 million coding sequences from 73 species representing all domains of life, as well as viruses, by means of our newly developed software PACKEIS. We show that codon composition and amino acid identity are main determinants of RNA secondary structure. In addition, we show that the arrangement of synonymous codons within coding sequences is non-random, yielding extremely high, but also extremely low, RNA structuredness significantly more often than expected by chance. Taken together, we demonstrate that selection for high and low levels of secondary structure is a widespread phenomenon. Our results provide another line of evidence that synonymous mutations are less neutral than commonly thought, which is of importance for many evolutionary models.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Maximiliano Distefano ◽  
Esteban Lanzarotti ◽  
María Florencia Fernández ◽  
Andrea Mangano ◽  
Marcelo Martí ◽  
...  

HIV Therapy ◽  
2009 ◽  
Vol 3 (6) ◽  
pp. 557-563 ◽  
Author(s):  
James Stephenson ◽  
Andrew Lever
Keyword(s):  

BMJ Open ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. e007334-e007334 ◽  
Author(s):  
H.-C. Tsai ◽  
P.-Y. Chou ◽  
S.-R. Wann ◽  
S. S.-J. Lee ◽  
Y.-S. Chen

1994 ◽  
Vol 22 (8) ◽  
pp. 1437-1443 ◽  
Author(s):  
David B. Oisen ◽  
Steven S. Carroll ◽  
J.Chris Culberson ◽  
Jules A. Shafer ◽  
Lawrence C. Kuo

2020 ◽  
Vol 34 (S1) ◽  
pp. 1-1
Author(s):  
Claudia Walker ◽  
Elisabeth Kan ◽  
Faith Davis ◽  
Jonathan Catazaro ◽  
Michael Summers

AIDS ◽  
2000 ◽  
Vol 14 (18) ◽  
pp. 2937-2939 ◽  
Author(s):  
Daniel R. Briggs ◽  
Daniel L. Tuttle ◽  
John W. Sleasman ◽  
Maureen M. Goodenow

mBio ◽  
2013 ◽  
Vol 4 (2) ◽  
Author(s):  
Adam W. Whisnant ◽  
Hal P. Bogerd ◽  
Omar Flores ◽  
Phong Ho ◽  
Jason G. Powers ◽  
...  

ABSTRACTThe question of how HIV-1 interfaces with cellular microRNA (miRNA) biogenesis and effector mechanisms has been highly controversial. Here, we first used deep sequencing of small RNAs present in two different infected cell lines (TZM-bl and C8166) and two types of primary human cells (CD4+peripheral blood mononuclear cells [PBMCs] and macrophages) to unequivocally demonstrate that HIV-1 does not encode any viral miRNAs. Perhaps surprisingly, we also observed that infection of T cells by HIV-1 has only a modest effect on the expression of cellular miRNAs at early times after infection. Comprehensive analysis of miRNA binding to the HIV-1 genome using the photoactivatable ribonucleoside-induced cross-linking and immunoprecipitation (PAR-CLIP) technique revealed several binding sites for cellular miRNAs, a subset of which were shown to be capable of mediating miRNA-mediated repression of gene expression. However, the main finding from this analysis is that HIV-1 transcripts are largely refractory to miRNA binding, most probably due to extensive viral RNA secondary structure. Together, these data demonstrate that HIV-1 neither encodes viral miRNAs nor strongly influences cellular miRNA expression, at least early after infection, and imply that HIV-1 transcripts have evolved to avoid inhibition by preexisting cellular miRNAs by adopting extensive RNA secondary structures that occlude most potential miRNA binding sites.IMPORTANCEMicroRNAs (miRNAs) are a ubiquitous class of small regulatory RNAs that serve as posttranscriptional regulators of gene expression. Previous work has suggested that HIV-1 might subvert the function of the cellular miRNA machinery by expressing viral miRNAs or by dramatically altering the level of cellular miRNA expression. Using very sensitive approaches, we now demonstrate that neither of these ideas is in fact correct. Moreover, HIV-1 transcripts appear to largely avoid regulation by cellular miRNAs by adopting an extensive RNA secondary structure that occludes the ability of cellular miRNAs to interact with viral mRNAs. Together, these data suggest that HIV-1, rather than seeking to control miRNA function in infected cells, has instead evolved a mechanism to become largely invisible to cellular miRNA effector mechanisms.


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