scholarly journals LncRNAs associated with glioblastoma: From transcriptional noise to novel regulators with a promising role in therapeutics

2021 ◽  
Vol 24 ◽  
pp. 728-742
Author(s):  
Bhupender Yadav ◽  
Sonali Pal ◽  
Yury Rubstov ◽  
Akul Goel ◽  
Manoj Garg ◽  
...  
2019 ◽  
Vol 2019 ◽  
pp. 1-12 ◽  
Author(s):  
Wenyuan Zhao ◽  
Yuanqi Liu ◽  
Chunfang Zhang ◽  
Chaojun Duan

Long noncoding RNAs (lncRNAs) are not transcriptional noise, as previously understood, but are currently considered to be multifunctional. Exosomes are derived from the internal multivesicular compartment and are extracellular vesicles (EVs) with diameters of 30–100 nm. Exosomes play significant roles in the intercellular exchange of information and material. Exosomal lncRNAs may be promising biomarkers for cancer diagnosis and potential targets for cancer therapies, since they are increasingly understood to be involved in tumorigenesis, tumor angiogenesis, and chemoresistance. This review mainly focuses on the roles of emerging exosomal lncRNAs in cancer. In addition, the biogenesis of exosomes, the functions of lncRNAs, and the mechanisms of lncRNAs in exosome-mediated cell-cell communication are also summarized.


2014 ◽  
Vol 106 (2) ◽  
pp. 494a
Author(s):  
Lotte Teufel ◽  
Aouefa Amoussouvi ◽  
Gabriele Schreiber ◽  
Edda Klipp ◽  
Andreas Herrmann

2013 ◽  
Vol 29 (6) ◽  
pp. 333-338 ◽  
Author(s):  
Daniel Hebenstreit

Genetics ◽  
2017 ◽  
Vol 208 (1) ◽  
pp. 173-189 ◽  
Author(s):  
Gustavo Valadares Barroso ◽  
Natasa Puzovic ◽  
Julien Y. Dutheil

2006 ◽  
Vol 24 (6) ◽  
pp. 853-865 ◽  
Author(s):  
William J. Blake ◽  
Gábor Balázsi ◽  
Michael A. Kohanski ◽  
Farren J. Isaacs ◽  
Kevin F. Murphy ◽  
...  

2008 ◽  
Vol 4 (7) ◽  
pp. e1000109 ◽  
Author(s):  
Namiko Mitarai ◽  
Ian B. Dodd ◽  
Michael T. Crooks ◽  
Kim Sneppen

1995 ◽  
Vol 349 (1329) ◽  
pp. 249-253 ◽  

Several proposals are made to explain the apparent increase in complexity of certain lineages during evolution. The proposals (not made in this order) are: (1) that gene number is a valid measure of biological complexity; (2) that gene number has not increased continuously during evolution, but has risen in discrete steps; (3) that two of the biggest steps occurred at the transition from prokaryotes to eukaryotes and the transition from invertebrates to vertebrates; (4) that these steps were made possible by ‘systemic’ changes in the way that genetic information is managed in the genome; (5) that the ability to silence inappropriate promoters is the primary limitation on gene number; (6) that the invention of nucleosomes (and perhaps the nuclear membrane) facilitated the evolution of eukaryotes from prokaryotic ancestors; (7) that the spread of low density methylation throughout the genome facilitated the evolution of vertebrates from invertebrate ancestors.


2006 ◽  
Vol 361 (1467) ◽  
pp. 495-506 ◽  
Author(s):  
S Ramsey ◽  
A Ozinsky ◽  
A Clark ◽  
K.D Smith ◽  
P de Atauri ◽  
...  

Transcriptional noise is known to play a crucial role in heterogeneity in bacteria and yeast. Mammalian macrophages are known to exhibit cell-to-cell variation in their responses to pathogens, but the source of this heterogeneity is not known. We have developed a detailed stochastic model of gene expression that takes into account scaling effects due to cell size and genome complexity. We report the results of applying this model to simulating gene expression variability in mammalian macrophages, demonstrating a possible molecular basis for heterogeneity in macrophage signalling responses. We note that the nature of predicted transcriptional noise in macrophages is different from that in yeast and bacteria. Some molecular interactions in yeast and bacteria are thought to have evolved to minimize the effects of the high-frequency noise observed in these species. Transcriptional noise in macrophages results in slow changes to gene expression levels and would not require the type of spike-filtering circuits observed in yeast and bacteria.


2017 ◽  
Author(s):  
John P. Lloyd ◽  
Zing Tsung-Yeh Tsai ◽  
Rosalie P. Sowers ◽  
Nicholas L. Panchy ◽  
Shin-Han Shiu

ABSTRACTWith advances in transcript profiling, the presence of transcriptional activities in intergenic regions has been well established. However, whether intergenic expression reflects transcriptional noise or activity of novel genes remains unclear. We identified intergenic transcribed regions (ITRs) in 15 diverse flowering plant species and found that the amount of intergenic expression correlates with genome size, a pattern that could be expected if intergenic expression is largely nonfunctional. To further assess the functionality of ITRs, we first built machine learning classifiers using Arabidopsis thaliana as a model that accurately distinguish functional sequences (phenotype genes) and likely nonfunctional ones (pseudogenes and unexpressed intergenic regions) by integrating 93 biochemical, evolutionary, and sequence-structure features. Next, by applying the models genome-wide, we found that 4,427 ITRs (38%) and 796 annotated ncRNAs (44%) had features significantly similar to benchmark protein-coding or RNA genes and thus were likely parts of functional genes. Approximately 60% of ITRs and ncRNAs were more similar to nonfunctional sequences and were likely transcriptional noise. The predictive framework established here provides not only a comprehensive look at how functional, genic sequences are distinct from likely nonfunctional ones, but also a new way to differentiate novel genes from genomic regions with noisy transcriptional activities.


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