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1.
Proc Natl Acad Sci U S A ; 119(36): e2118763119, 2022 09 06.
Article in English | MEDLINE | ID: mdl-36037356

ABSTRACT

Turritopsis dohrnii is the only metazoan able to rejuvenate repeatedly after its medusae reproduce, hinting at biological immortality and challenging our understanding of aging. We present and compare whole-genome assemblies of T. dohrnii and the nonimmortal Turritopsis rubra using automatic and manual annotations, together with the transcriptome of life cycle reversal (LCR) process of T. dohrnii. We have identified variants and expansions of genes associated with replication, DNA repair, telomere maintenance, redox environment, stem cell population, and intercellular communication. Moreover, we have found silencing of polycomb repressive complex 2 targets and activation of pluripotency targets during LCR, which points to these transcription factors as pluripotency inducers in T. dohrnii. Accordingly, we propose these factors as key elements in the ability of T. dohrnii to undergo rejuvenation.


Subject(s)
Hydrozoa , Rejuvenation , Animals , Genomics , Hydrozoa/genetics , Hydrozoa/growth & development , Life Cycle Stages/genetics , Transcriptome
2.
Sci Rep ; 9(1): 14938, 2019 10 17.
Article in English | MEDLINE | ID: mdl-31624306

ABSTRACT

Tardigrades, also known as water bears, are small aquatic animals that inhabit marine, fresh water or limno-terrestrial environments. While all tardigrades require surrounding water to grow and reproduce, species living in limno-terrestrial environments (e.g. Ramazzottius varieornatus) are able to undergo almost complete dehydration by entering an arrested state known as anhydrobiosis, which allows them to tolerate ionic radiation, extreme temperatures and intense pressure. Previous studies based on comparison of the genomes of R. varieornatus and Hypsibius dujardini - a less tolerant tardigrade - have pointed to potential mechanisms that may partially contribute to their remarkable ability to resist extreme physical conditions. In this work, we have further annotated the genomes of both tardigrades using a guided approach in search for novel mechanisms underlying the extremotolerance of R. varieornatus. We have found specific amplifications of several genes, including MRE11 and XPC, and numerous missense variants exclusive of R. varieornatus in CHEK1, POLK, UNG and TERT, all of them involved in important pathways for DNA repair and telomere maintenance. Taken collectively, these results point to genomic features that may contribute to the enhanced ability to resist extreme environmental conditions shown by R. varieornatus.


Subject(s)
Adaptation, Physiological/genetics , Extremophiles/physiology , Genome/physiology , Molecular Sequence Annotation , Tardigrada/physiology , Animals , Gene Amplification , Genomics , Mutation, Missense , Water
3.
Methods Mol Biol ; 1881: 319-325, 2019.
Article in English | MEDLINE | ID: mdl-30350214

ABSTRACT

The genomic sequencing of chronic lymphocytic leukemia (CLL) samples has provided exciting new venues for the understanding and treatment of this prevalent disease. This feat is possible thanks to high-throughput sequencing methods, such as Illumina sequencing. The interpretation of these data sources requires not only appropriate software and hardware, but also understanding the biology and technology behind the sequencing process. Here, we provide a primer to understand each step in the analysis of point mutations from whole-genome or whole-exome sequencing experiments of tumor and normal samples.


Subject(s)
Computational Biology/methods , Genetic Variation , Genome, Human , High-Throughput Nucleotide Sequencing/methods , Leukemia, Lymphocytic, Chronic, B-Cell/genetics , Sequence Analysis, DNA/methods , Whole Genome Sequencing/methods , Humans , Software
4.
Nat Ecol Evol ; 3(1): 87-95, 2019 01.
Article in English | MEDLINE | ID: mdl-30510174

ABSTRACT

Giant tortoises are among the longest-lived vertebrate animals and, as such, provide an excellent model to study traits like longevity and age-related diseases. However, genomic and molecular evolutionary information on giant tortoises is scarce. Here, we describe a global analysis of the genomes of Lonesome George-the iconic last member of Chelonoidis abingdonii-and the Aldabra giant tortoise (Aldabrachelys gigantea). Comparison of these genomes with those of related species, using both unsupervised and supervised analyses, led us to detect lineage-specific variants affecting DNA repair genes, inflammatory mediators and genes related to cancer development. Our study also hints at specific evolutionary strategies linked to increased lifespan, and expands our understanding of the genomic determinants of ageing. These new genome sequences also provide important resources to help the efforts for restoration of giant tortoise populations.


Subject(s)
Aging/genetics , Genome , Turtles/genetics , Animals , DNA Repair/genetics , Evolution, Molecular , HEK293 Cells , Humans , Inflammation Mediators , Male , Neoplasms/genetics , Phylogeny , Population Density
5.
Bioinformatics ; 34(13): 2322-2324, 2018 07 01.
Article in English | MEDLINE | ID: mdl-29949954

ABSTRACT

Motivation: Venn and Euler diagrams are extensively used for the visualization of relationships between experiments and datasets. However, representing more than three datasets while keeping the proportions of each region is still not feasible with existing tools. Results: We present an algorithm to render all the regions of a generalized n-dimensional Venn diagram, while keeping the area of each region approximately proportional to the number of elements included. In addition, missing regions in Euler diagrams lead to simplified representations. The algorithm generates an n-dimensional Venn diagram and inserts circles of given areas in each region. Then, the diagram is rearranged with a dynamic, self-correcting simulation in which each set border is contracted until it contacts the circles inside. This algorithm is implemented in a C++ tool (nVenn) with or without a web interface. The web interface also provides the ability to analyze the regions of the diagram. Availability and implementation: The source code and pre-compiled binaries of nVenn are available at https://github.com/vqf/nVenn. A web interface for up to six sets can be accessed at http://degradome.uniovi.es/cgi-bin/nVenn/nvenn.cgi. Supplementary information: Supplementary data are available at Bioinformatics online.


Subject(s)
Software , Algorithms
6.
Genome Biol Evol ; 9(12): 3260-3264, 2017 12 01.
Article in English | MEDLINE | ID: mdl-28985367

ABSTRACT

The sperm whale, made famous by Moby Dick, is one of the most fascinating of all ocean-dwelling species given their unique life history, novel physiological adaptations to hunting squid at extreme ocean depths, and their position as one of the earliest branching toothed whales (Odontoceti). We assembled the sperm whale (Physeter macrocephalus) genome and resequenced individuals from multiple ocean basins to identify new candidate genes for adaptation to an aquatic environment and infer demographic history. Genes crucial for skin integrity appeared to be particularly important in both the sperm whale and other cetaceans. We also find sperm whales experienced a steep population decline during the early Pleistocene epoch. These genomic data add new comparative insight into the evolution of whales.


Subject(s)
Evolution, Molecular , Genome , Sperm Whale/genetics , Animals , DNA, Mitochondrial/genetics , Phylogeny
7.
Nucleic Acids Res ; 44(D1): D351-5, 2016 Jan 04.
Article in English | MEDLINE | ID: mdl-26553809

ABSTRACT

Since the definition of the degradome as the complete repertoire of proteases in a given organism, the combined effort of numerous laboratories has greatly expanded our knowledge of its roles in biology and pathology. Once the genomic sequences of several important model organisms were made available, we presented the Degradome database containing the curated sets of known protease genes in human, chimpanzee, mouse and rat. Here, we describe the updated Degradome database, featuring 81 new protease genes and 7 new protease families. Notably, in this short time span, the number of known hereditary diseases caused by mutations in protease genes has increased from 77 to 119. This increase reflects the growing interest on the roles of the degradome in multiple diseases, including cancer and ageing. Finally, we have leveraged the widespread adoption of new webtools to provide interactive graphic views that show information about proteases in the global context of the degradome. The Degradome database can be accessed through its web interface at http://degradome.uniovi.es.


Subject(s)
Databases, Protein , Peptide Hydrolases/genetics , Animals , Genetic Diseases, Inborn/genetics , Humans , Mice , Molecular Sequence Annotation , Mutation , Rats
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