Deep learning reveals determinants of transcriptional infidelity at nucleotide resolution in the allopolyploid line by goldfish and common carp hybrids.
Kaizhuang Jing, Tingchu Wei, Xuedie Gu, Guoliang Lin, Lin Liu, Jing Luo
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引用次数: 0
Abstract
During DNA transcription, the central dogma states that DNA generates corresponding RNA sequences based on the principle of complementary base pairing. However, in the allopolyploid line by goldfish and common carp hybrids, there is a significant level of transcriptional infidelity. To explore deeper into the causes of transcriptional infidelity in this line, we developed a deep learning model to explore its underlying determinants. First, our model can accurately identify transcriptional infidelity sequences at the nucleotide resolution and effectively distinguish transcriptional infidelity regions at the subregional level. Subsequently, we utilized this model to quantitatively assess the importance of position-specific motifs. Furthermore, by integrating the relationship between transcription factors and their recognition motifs, we unveiled the distribution of position-specific transcription factor families and classes that influence transcriptional infidelity in this line. In summary, our study provides new insights into the deeper determinants of transcriptional infidelity in this line.
期刊介绍:
Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data.
The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.