scholarly journals Genome-level analyses of Mycobacterium bovis lineages reveal the role of SNPs and antisense transcription in differential gene expression

BMC Genomics ◽  
2013 ◽  
Vol 14 (1) ◽  
pp. 710 ◽  
Author(s):  
Paul Golby ◽  
Javier Nunez ◽  
Adam Witney ◽  
Jason Hinds ◽  
Michael A Quail ◽  
...  
2001 ◽  
Vol 94 (5) ◽  
pp. 674-684 ◽  
Author(s):  
Boris P.-L. Lee ◽  
Walter J. Rushlow ◽  
Chandan Chakraborty ◽  
Peeyush K. Lala

Peptides ◽  
2004 ◽  
Vol 25 (7) ◽  
pp. 1107-1114 ◽  
Author(s):  
Hisamitsu Onitsuka ◽  
Takuroh Imamura ◽  
Kaoru Ito ◽  
Kenji Kuwasako ◽  
Hiroshi Yamakawa ◽  
...  

2018 ◽  
Author(s):  
Clément Rougeux ◽  
Pierre-Alexandre Gagnaire ◽  
Kim Praebel ◽  
Ole Seehausen ◽  
Louis Bernatchez

ABSTRACTIn contrast to the plethora of studies focusing on the genomic basis of adaptive phenotypic divergence, the role of gene expression during speciation has been much less investigated and consequently, less understood. Yet, the convergence of differential gene expression patterns between closely related species-pairs might reflect the role of natural selection during the process of ecological speciation. Here, we test for intercontinental convergence in differential transcriptional signatures between limnetic and benthic sympatric species-pairs of Lake Whitefish (Coregonus clupeaformis) and its sister-lineage, the European Whitefish (C. lavaretus), using six replicated sympatric species-pairs (two in North America, two in Norway and two in Switzerland). We characterized both sequence variation in transcribed regions and differential gene expression between sympatric limnetic and benthic species across regions and continents. Our first finding was that differentially expressed genes (DEG) between limnetic and benthic whitefish tend to be enriched in shared polymorphism among sister-lineages. We then used both genotypes and co-variation in expression in order to infer polygenic selection at the gene level. We identified parallel outliers and DEG involving genes primarily over-expressed in limnetic species relative to the benthic species. Our analysis finally revealed the existence of shared genomic bases underlying parallel differential expression across replicated species pairs from both continents, such as a cis-eQTL affecting the pyruvate kinase expression level involved in glycolysis. Our results are consistent with a longstanding role of natural selection in maintaining transcontinental diversity at phenotypic traits involved in ecological speciation between limnetic and benthic whitefishes.


2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Elise Matuzelski ◽  
Alexandra Essebier ◽  
Lachlan Harris ◽  
Richard M. Gronostajski ◽  
Tracey J. Harvey ◽  
...  

Abstract Objective Nuclear Factor One X (NFIX) is a transcription factor expressed by neural stem cells within the developing mouse brain and spinal cord. In order to characterise the pathways by which NFIX may regulate neural stem cell biology within the developing mouse spinal cord, we performed an microarray-based transcriptomic analysis of the spinal cord of embryonic day (E)14.5 Nfix−/− mice in comparison to wild-type controls. Data description Using microarray and differential gene expression analyses, we were able to identify differentially expressed genes in the spinal cords of E14.5 Nfix−/− mice compared to wild-type controls. We performed microarray-based sequencing on spinal cords from n = 3 E14.5 Nfix−/− mice and n = 3 E14.5 Nfix+/+ mice. Differential gene expression analysis, using a false discovery rate (FDR) p-value of p < 0.05, and a fold change cut-off for differential expression of >  ± 1.5, revealed 1351 differentially regulated genes in the spinal cord of Nfix−/− mice. Of these, 828 were upregulated, and 523 were downregulated. This resource provides a tool to interrogate the role of this transcription factor in spinal cord development.


2017 ◽  
Vol 113 ◽  
pp. 480-489 ◽  
Author(s):  
Sanjeev Kumar Shukla ◽  
Shubhra Shukla ◽  
Anuj Chauhan ◽  
Sarvjeet ◽  
Rehan Khan ◽  
...  

2019 ◽  
Vol 20 (6) ◽  
pp. 405-408
Author(s):  
Luis M. Vaschetto ◽  
Natalia Ortiz

Sequence duplication is nowadays recognized as an important mechanism that underlies the evolution of eukaryote genomes, being indeed one of the most powerful strategies for the generation of adaptive diversity by modulating transcriptional activity. The evolutionary novelties simultaneously associated with sequence duplication and differential gene expression can be collectively referred to as duplication-mediated transcriptional regulation. In the last years, evidence has emerged supporting the idea that sequence duplication and functionalization represent important evolutionary strategies acting at the genome level, and both coding and non-coding sequences have been found to be targets of such events. Moreover, it has been proposed that deleterious effects of sequence duplication might be potentially silenced by endogenous cell machinery (i.e., RNA interference, epigenetic repressive marks, etc). Along these lines, our aim is to highlight the role of sequence duplication on transcriptional activity and the importance of both in genome evolution.


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