scholarly journals Genome-Wide Analysis of Alternative Splicing during Host-Virus Interactions in Chicken

Viruses ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2409
Author(s):  
Weiwei Liu ◽  
Yingjie Sun ◽  
Xusheng Qiu ◽  
Chunchun Meng ◽  
Cuiping Song ◽  
...  

The chicken is a model animal for the study of evolution, immunity and development. In addition to their use as a model organism, chickens also represent an important agricultural product. Pathogen invasion has already been shown to modulate the expression of hundreds of genes, but the role of alternative splicing in avian virus infection remains unclear. We used RNA-seq data to analyze virus-induced changes in the alternative splicing of Gallus gallus, and found that a large number of alternative splicing events were induced by virus infection both in vivo and in vitro. Virus-responsive alternative splicing events preferentially occurred in genes involved in metabolism and transport. Many of the alternatively spliced transcripts were also expressed from genes with a function relating to splicing or immune response, suggesting a potential impact of virus infection on pre-mRNA splicing and immune gene regulation. Moreover, exon skipping was the most frequent AS event in chickens during virus infection. This is the first report describing a genome-wide analysis of alternative splicing in chicken and contributes to the genomic resources available for studying host–virus interaction in this species. Our analysis fills an important knowledge gap in understanding the extent of genome-wide alternative splicing dynamics occurring during avian virus infection and provides the impetus for the further exploration of AS in chicken defense signaling and homeostasis.

2014 ◽  
Author(s):  
Kjong-Van Lehmann ◽  
Andre Kahles ◽  
Cyriac Kandoth ◽  
William Lee ◽  
Nikolaus Schultz ◽  
...  

We present a genome-wide analysis of splicing patterns of 282 kidney renal clear cell carcinoma patients in which we integrate data from whole-exome sequencing of tumor and normal samples, RNA-seq and copy number variation. We proposed a scoring mechanism to compare splicing pat- terns in tumor samples to normal samples in order to rank and detect tumor-specific isoforms that have a potential for new biomarkers. We identified a subset of genes that show introns only observable in tumor but not in normal samples, ENCODE and GEUVADIS samples. In order to improve our understanding of the underlying genetic mechanisms of splicing variation we performed a large-scale association analysis to find links between somatic or germline variants with alternative splicing events. We identified 915 cis- and trans-splicing quantitative trait loci (sQTL) associated with changes in splicing patterns. Some of these sQTL have previously been associated with being susceptibility loci for cancer and other diseases. Our analysis also allowed us to identify the function of several COSMIC variants showing significant association with changes in alternative splicing. This demonstrates the potential significance of variants affecting alternative splicing events and yields insights into the mechanisms related to an array of disease phenotypes.


2019 ◽  
Vol 37 (5-6) ◽  
pp. 413-420 ◽  
Author(s):  
Abozar Ghorbani ◽  
Ahmad Tahmasebi ◽  
Keramatollah Izadpanah ◽  
Alireza Afsharifar ◽  
Ralf G. Dietzgen

FEBS Letters ◽  
2015 ◽  
Vol 589 (23) ◽  
pp. 3564-3575 ◽  
Author(s):  
Bahman Panahi ◽  
Seyed Abolghasem Mohammadi ◽  
Reyhaneh Ebrahimi Khaksefidi ◽  
Jalil Fallah Mehrabadi ◽  
Esmaeil Ebrahimie

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