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Biology subjects

Sandvik, G. K.

Publications and source records attributed to Sandvik, G. K..

3 recordsLinked to original sources

Comparative transcriptomic analysis defines shared and mammary-specific gene expression programs across glandular tissues

The mammary gland represents a defining evolutionary innovation of mammals, which is an epithelial tissue with specialized secretory functions that are regulated by hormonal and transcriptional processes. While mammary differentiation has been extensively studied, its transcriptional relationship to other epithelial tissues with secretory activity has been less explored in an evolutionary context. Here, we used bulk RNA-seq data from the GTEx project to examine gene expression patterns in human breast tissue alongside a set of other tissues that contain epithelial secretory components, as well as non-glandular tissues. Using cross-tissue differential expression analyses, co-expression network analysis, and integration with single-cell expression references, we characterized patterns of gene expression that recur across multiple secretory tissues and those that show relative enrichment in breast tissue. This analysis highlights three broad classes of expression patterns: genes with elevated expression across several secretory tissues, genes showing preferential expression in breast tissue, and genes displaying sex-associated differences in breast samples. These gene sets are associated with distinct functional annotations, including epithelial structure, metabolic and hormone-responsive processes, and immune-related functions. Comparative analyses of gene conservation indicate that many genes preferentially expressed in breast tissue are evolutionarily conserved across vertebrates, consistent with the reuse of pre-existing gene repertoires in the mammalian lineage in tissue-specific contexts. Together, these results support a model in which breast tissue identity reflects the regulatory re-weighting and integration of conserved epithelial secretory modules rather than lineage-specific gene innovation. By placing human breast tissue gene expression in a comparative and evolutionary context, this study provides a molecular framework for understanding how complex organ-level traits arise through regulatory modularity. SignificanceThe mammary gland is a defining feature of mammals, yet it remains unclear how its gene activity relates to that of other tissues with similar secretory functions. By comparing gene expression in human breast tissue with other epithelial secretory tissues, this study shows that much of breast tissue gene expression is shared with a common epithelial program, while a smaller set of genes is associated with breast-specific metabolic and hormonal functions. These findings help clarify how mammary gland specialization arises in mammalian lineages from ancestral genetic materials rather than from entirely new gene emergences, providing a framework for understanding the evolution of new organs.

genomics↗

Investigating antiviral pathways in Atlantic salmon cells through interferon receptor knockouts via CRISPR-Cas9

In Atlantic salmon (Salmo salar), infectious salmon anemia virus (ISAV) and infectious pancreatic necrosis virus (IPNV) evade host immune response through complex antagonistic mechanisms. Type I interferons (IFNs) play a pivotal role in antiviral defense by signaling through heterodimeric receptors to activate the JAK-STAT pathway and drives the expression of interferon-stimulated genes (ISGs). In this study, CRISPR-Cas9 was used to knock out (KO) interferon receptor genes (crfb1a, crfb5a, il10rb, ifngr2a) and a combined group of candidate receptors (crfb1a, crfb5a, il10rb, ifngr2a, il10r2) to investigate their roles and their impact on downstream signaling cascades with RNA sequencing. Recombinant IFNa was used to induce an antiviral state before challenging cells with ISAV and IPNV. The knockouts significantly disrupt downstream antiviral signaling, with two knockouts, crfb1a and crfb5a, showing pronounced effects. During ISAV infection, the crfb1a KO group exhibited a marked reduction in the expression of critical signaling genes such as stat1b, stat2, stat6, and irf3 during ISAV infection, while irf7 was upregulated during IPNV infection. The crfb5a KO group exhibited reduced stat2 expression in ISAV infection and upregulated irf7 during IPNV infection. Despite these disruptions, ISGs such as Mx and isg15 maintained their expression levels across all knockout groups, suggesting potential alternative signaling pathways. Pathway analysis further revealed upregulation of cellular processes like actin regulation and phagosome activity, which may compensate for impaired immune signaling. These findings highlight the distinct roles of IFN receptor genes in mediating antiviral responses and underscore the complexity of IFN signaling in Atlantic salmon.

immunology↗

Functional and regulatory diversification of circadian rhythm period genes during the evolution of vertebrates

The Period genes (Per) play essential roles in modulating the molecular circadian clock timing in a broad range of species, which regulates the physiological and cellular through the transcription-translation feedback loop. While the Period gene paralogs are widely observed among vertebrates, the evolutionary history and the functional diversification of Per genes across vertebrates are not well known. In this study, we comprehensively investigated the evolution of Per genes, including de novo binding motif discovery by comparative genomics. We also determined the lineage-specific transcriptome landscape across tissues and developmental stages and phenotypic effects in public RNA-seq data sets of model species. We observed multiple lineage-specific gain and loss events of Per genes, though no simple association was observed between ecological factors and Per gene numbers in each species. Among salmonid fish species, the per3 gene has been lost in the majority, whereas those retaining the per3 gene exhibit not a signature of relaxed selective constraint but rather a signature of intensified selection. We also determined the signature of adaptive diversification of the CRY-binding region in Per1 and Per3, which modulates the circadian rhythm. We also discovered putative regulatory sequences, which are lineage-specific, suggesting that these cis-regulatory elements may have evolved rapidly and divergently across different lineages. Collectively, our findings revealed the evolution of Per genes and their fine-tuned contribution to the plastic and precise regulation of circadian rhythms in various vertebrate taxa. SignificanceThe Period (Per) genes play essential roles in the circadian rhythm in animals. In this study, we comprehensively investigated the evolutionary diversification of the three types of Period genes in vertebrates. As a result, we observed a rapid evolution and sub-functionalization of these genes, especially adaptive diversification signatures in the protein-binding region, which plays a crucial role in regulating circadian rhythms. This underscores the fine-tuned contribution of Per genes in the biological clocks precision and adaptability across various vertebrate taxa.

evolutionary biology↗