Biology subjects

Vasquez, Y. M.

Publications and source records attributed to Vasquez, Y. M..

3 recordsLinked to original sources

bioRxiv2025

Genome-resolved expansion of Nucleocytoviricota and Mirusviricota reveals new diversity, functional potential, and biotechnological applications

Nucleocytoplasmic large DNA viruses (NCLDV) of the phyla Nucleocytoviricota and viruses of the newly proposed Duplodnaviria phylum, Mirusviricota, exhibit taxonomic richness which continues to expand due to metagenomic sequencing of Earths biomes. Giant viruses contain complex genomes encoding genes of both viral and cellular origin, representing a reservoir of unexplored biological functions with potential implications for ecology, evolution, and biotechnology. Here, we present the largest curated database of giant virus metagenome-assembled genomes (GVMAGs V2), comprising 8,508 species-level clusters inferred from 18,727 genomes, originating from marine, freshwater, anthropogenic and terrestrial environments, a six-fold increase from the previous giant virus phylogenetic frameworks. Phylogenomics and relative evolutionary distance analysis revealed 712 novel genera, 13 previously unknown viral families and a new proposed order, tentatively named Mycodnavirales. We improved gene calling of 12% of giant virus genomes by accounting for alternative and custom genetic codes, enabling more accurate identification of protein-coding genes. Database mining uncovered endogenous viral elements in a broad spectrum of eukaryotes, spanning algae, fungi, and parasitic protists highlighting that giant virus integration is both widespread and evolutionarily persistent. Orthologous clustering of 2.5 million proteins identified 135,998 orthogroups representing comprehensive metabolic capabilities, such as enrichment of genes involved in aromatic compound degradation (commonly associated with bioremediation) in Algavirales genomes. Furthermore, we detected widespread biosynthetic gene clusters underpinning antimicrobial activity and antibiotic resistance, suggesting roles of giant viruses in host defense and in the dissemination of antibiotic resistance genes. Conversely, 67% of orthogroups have unknown functions, underscoring a substantial unexplored potential. This comprehensive publicly available database provides a critical resource for the giant virus research community and a foundation for uncovering virus-host interactions, exploring viral evolution, and identifying reservoirs for novel enzymes with the potential to advance biotechnological applications.

microbiology↗

bioRxiv2021

Gene structure, differential exon usage, and expression of the testis long intergenic non-protein coding RNA 1016 in humans reveals isoform-specific roles in controlling biological processes

Long noncoding RNAs (lncRNAs) have emerged as critical regulators of biological processes. The constant expansion of newly-identified lncRNA genes requires that each one be comprehensively annotated to understand its molecular functions. Here, we describe a detailed characterization of the gene which encodes long intergenic non-protein coding RNA 01016 (LINC01016, a.k.a., LncRNA1195) with a focus on its structure, exon usage, and expression in human and macaque tissues. In this study, we show that it is exclusively conserved among non-human primates, suggesting its recent evolution and is expressed and processed into 12 distinct RNAs in testis, cervix, and uterus tissues. Further, we integrate de novo annotation of expressed LINC01016 transcripts and isoform-dependent gene expression analyses to show that human LINC01016 is a multi-exon gene, processed through differential exon usage with isoform-specific functions. Furthermore, in gynecological cancers, such as cervical squamous cell carcinoma and uterine corpus endometrial carcinoma, LINC01016 is downregulated; however, its higher expression is predictive of relapse-free survival in these cancers. Collectively, these analyses reveal that, unlike coding RNAs, lncRNA isoforms are differentially regulated and precisely processed in specific tissues to perform distinct biological roles. One sentence summaryThe distinct molecular role of LINC01016 isoforms reveals intricate biology associated with lncRNA transcription and processing.

genomics↗

bioRxiv2020

Mutational pressure drives differential genome conservation in two bacterial endosymbionts of sap feeding insects

Compared to free-living bacteria, endosymbionts of sap-feeding insects have tiny and rapidly evolving genomes. Increased genetic drift, high mutation rates, and relaxed selection associated with host control of key cellular functions all likely contribute to genome decay. Phylogenetic comparisons have revealed massive variation in endosymbiont evolutionary rate, but such methods make it difficult to partition the effects of mutation vs. selection. For example, the ancestor of auchenorrhynchan insects contained two obligate endosymbionts, Sulcia and a betaproteobacterium (BetaSymb; called Nasuia in leafhoppers) that exhibit divergent rates of sequence evolution and different propensities for loss and replacement in the ensuing [~]300 Ma. Here, we use the auchenorrhynchan leafhopper Macrosteles sp. nr. severini, which retains both of the ancestral endosymbionts, to test the hypothesis that differences in evolutionary rate are driven by differential mutagenesis. We used a high-fidelity technique known as duplex sequencing to measure and compare low-frequency variants in each endosymbiont. Our direct detection of de novo mutations reveals that the rapidly evolving endosymbiont (Nasuia) has a much higher frequency of single-nucleotide variants than the more stable endosymbiont (Sulcia) and a mutation spectrum that is even more AT-biased than implied by the 83.1% AT content of its genome. We show that indels are common in both endosymbionts but differ substantially in length and distribution around repetitive regions. Our results suggest that differences in long-term rates of sequence evolution in Sulcia vs. BetaSymb, and perhaps the contrasting degrees of stability of their relationships with the host, are driven by differences in mutagenesis. SIGNIFICANCE STATEMENTTwo ancient endosymbionts in the same host lineage display stark differences in genome conservation over phylogenetic scales. We show the rapidly evolving endosymbiont has a higher frequency of mutations, as measured with duplex sequencing. Therefore, differential mutagenesis likely drives evolutionary rate variation in these endosymbionts.

genetics↗