GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6643 ( 2023-04-28)
    Abstract: A major challenge in genomics is discerning which bases among billions alter organismal phenotypes and affect health and disease risk. Evidence of past selective pressure on a base, whether highly conserved or fast evolving, is a marker of functional importance. Bases that are unchanged in all mammals may shape phenotypes that are essential for organismal health. Bases that are evolving quickly in some species, or changed only in species that share an adaptive trait, may shape phenotypes that support survival in specific niches. Identifying bases associated with exceptional capacity for cellular recovery, such as in species that hibernate, could inform therapeutic discovery. RATIONALE The power and resolution of evolutionary analyses scale with the number and diversity of species compared. By analyzing genomes for hundreds of placental mammals, we can detect which individual bases in the genome are exceptionally conserved (constrained) and likely to be functionally important in both coding and noncoding regions. By including species that represent all orders of placental mammals and aligning genomes using a method that does not require designating humans as the reference species, we explore unusual traits in other species. RESULTS Zoonomia’s mammalian comparative genomics resources are the most comprehensive and statistically well-powered produced to date, with a protein-coding alignment of 427 mammals and a whole-genome alignment of 240 placental mammals representing all orders. We estimate that at least 10.7% of the human genome is evolutionarily conserved relative to neutrally evolving repeats and identify about 101 million significantly constrained single bases (false discovery rate 〈 0.05). We cataloged 4552 ultraconserved elements at least 20 bases long that are identical in more than 98% of the 240 placental mammals. Many constrained bases have no known function, illustrating the potential for discovery using evolutionary measures. Eighty percent are outside protein-coding exons, and half have no functional annotations in the Encyclopedia of DNA Elements (ENCODE) resource. Constrained bases tend to vary less within human populations, which is consistent with purifying selection. Species threatened with extinction have few substitutions at constrained sites, possibly because severely deleterious alleles have been purged from their small populations. By pairing Zoonomia’s genomic resources with phenotype annotations, we find genomic elements associated with phenotypes that differ between species, including olfaction, hibernation, brain size, and vocal learning. We associate genomic traits, such as the number of olfactory receptor genes, with physical phenotypes, such as the number of olfactory turbinals. By comparing hibernators and nonhibernators, we implicate genes involved in mitochondrial disorders, protection against heat stress, and longevity in this physiologically intriguing phenotype. Using a machine learning–based approach that predicts tissue-specific cis - regulatory activity in hundreds of species using data from just a few, we associate changes in noncoding sequence with traits for which humans are exceptional: brain size and vocal learning. CONCLUSION Large-scale comparative genomics opens new opportunities to explore how genomes evolved as mammals adapted to a wide range of ecological niches and to discover what is shared across species and what is distinctively human. High-quality data for consistently defined phenotypes are necessary to realize this potential. Through partnerships with researchers in other fields, comparative genomics can address questions in human health and basic biology while guiding efforts to protect the biodiversity that is essential to these discoveries. Comparing genomes from 240 species to explore the evolution of placental mammals. Our new phylogeny (black lines) has alternating gray and white shading, which distinguishes mammalian orders (labeled around the perimeter). Rings around the phylogeny annotate species phenotypes. Seven species with diverse traits are illustrated, with black lines marking their branch in the phylogeny. Sequence conservation across species is described at the top left. IMAGE CREDIT: K. MORRILL
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 383, No. 6690 ( 2024-03-29)
    Abstract: Vocal production learning (“vocal learning”), or the ability to modify vocalizations according to the social environment, forms the basis of human speech production. Among the Boreoeutherian mammals, this trait has evolved independently in four different lineages: humans, bats, cetaceans, and pinnipeds. In vertebrates, the evolution of vocal learning behavior has been associated with the evolution of brain anatomical features, including cortical long-range projection neurons (e.g., songbirds and humans). Moreover, neural circuits for the production of learned vocalization display convergent evolution in patterns of gene expression. RATIONALE Despite evidence for the convergent evolution of vocal learning at the behavioral, anatomical, and gene expression levels in vertebrates, the genetic underpinnings of vocal learning and human speech in mammals are poorly understood. New machine learning approaches and the newly sequenced mammalian genomes of the Zoonomia Consortium provide the foundation to rigorously study this question. The repeated evolution of vocal learning across mammals allows us to determine which parts of the genome are significantly associated with the behavior. RESULTS First, we studied convergent evolution in protein-coding regions using the RERconverge and HyPhy methods to find 200 significantly associated genes. The genes that tend to be under higher constraint in vocal learning mammals are enriched for genes involved in human autism. However, the vast majority of genes are driven by signals from only one or two clades of vocal learning mammals, suggesting that a large component of the genetic basis for the trait may lie instead in the convergent evolution of regulatory elements. To explore that hypothesis, we performed an anatomical and functional characterization of the Egyptian fruit bat motor cortex. We identified a subregion of the motor cortex that is implicated in vocal production and directly projects to the motoneurons controlling the bat’s larynx. This allowed us to profile candidate regulatory elements active in this vocalization-associated subregion of the motor cortex by measuring open chromatin. These open chromatin regions and 222 mammalian genomes of the Zoonomia Consortium served as input to the Tissue-Aware Conservation Inference Toolkit (TACIT) machine learning approach, which was applied to find 50 candidate regulatory elements whose predicted motor cortex open chromatin measurements across mammals are highly correlated with the presence of vocal learning behavior. Many of these open chromatin regions were near genes associated with autism, and they tended to overlap with open chromatin specific to the long-range projection neurons that have been implicated in the evolution of vocal learning. CONCLUSION Although it is impossible to know which parts of the genome evolved for human speech production, we are able to use the repeated evolution of a component of that behavior, vocal learning, to find significantly associated genes and noncoding regions. Our results demonstrate that the presence of vocal learning behavior in a given clade leads to weak selective pressure across a broad range of genes and stronger selective pressure across a smaller number of motor cortex noncoding regions. These genes and noncoding regions show an association with autism, which suggests that there are shared regulatory networks for vocal and social behavior that tend to adapt in similar ways when a lineage evolves vocal learning behavior. More broadly, our results suggest that the evolutionary history of selective pressures across a location in the genome can provide insight into how that region might influence human behavior. Finding vocal learning–associated regions of the mammalian genome. We compared the evolution of vocal learning behavior to the evolution of coding and noncoding elements of the genome, leveraging anatomical, electrophysiological, and epigenomic experiments in the Egyptian fruit bat orofacial motor cortex (ofM1). We show convergent evidence of the importance of long-range projection neurons and autism-associated gene networks.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2024
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2022
    In:  Proceedings of the National Academy of Sciences Vol. 119, No. 40 ( 2022-10-04)
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 119, No. 40 ( 2022-10-04)
    Abstract: Decrypting the rearrangements that drive mammalian chromosome evolution is critical to understanding the molecular bases of speciation, adaptation, and disease susceptibility. Using 8 scaffolded and 26 chromosome-scale genome assemblies representing 23/26 mammal orders, we computationally reconstructed ancestral karyotypes and syntenic relationships at 16 nodes along the mammalian phylogeny. Three different reference genomes (human, sloth, and cattle) representing phylogenetically distinct mammalian superorders were used to assess reference bias in the reconstructed ancestral karyotypes and to expand the number of clades with reconstructed genomes. The mammalian ancestor likely had 19 pairs of autosomes, with nine of the smallest chromosomes shared with the common ancestor of all amniotes (three still conserved in extant mammals), demonstrating a striking conservation of synteny for ∼320 My of vertebrate evolution. The numbers and types of chromosome rearrangements were classified for transitions between the ancestral mammalian karyotype, descendent ancestors, and extant species. For example, 94 inversions, 16 fissions, and 14 fusions that occurred over 53 My differentiated the therian from the descendent eutherian ancestor. The highest breakpoint rate was observed between the mammalian and therian ancestors (3.9 breakpoints/My). Reconstructed mammalian ancestor chromosomes were found to have distinct evolutionary histories reflected in their rates and types of rearrangements. The distributions of genes, repetitive elements, topologically associating domains, and actively transcribed regions in multispecies homologous synteny blocks and evolutionary breakpoint regions indicate that purifying selection acted over millions of years of vertebrate evolution to maintain syntenic relationships of developmentally important genes and regulatory landscapes of gene-dense chromosomes.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2022
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6643 ( 2023-04-28)
    Abstract: It has been almost 100 years since the sled dog Balto helped save the community of Nome, Alaska, from a diphtheria outbreak. Today, Balto symbolizes the indomitable spirit of the sled dog. He is immortalized in statue and film, and is physically preserved and on display at the Cleveland Museum of Natural History. Balto represents a dog population that was reputed to tolerate harsh conditions at a time when northern communities were reliant on sled dogs. Investigating Balto’s genome sequence using technologies for sequencing degraded DNA offers a new perspective on this historic population. RATIONALE Analyzing high-coverage (40.4-fold) DNA sequencing data from Balto through comparison with large genomic data resources offers an opportunity to investigate genetic diversity and genome function. We leveraged the genome sequence data from 682 dogs, including both working sled dogs and dog breeds, as well as evolutionary constraint scores from the Zoonomia alignment of 240 mammals, to reconstruct Balto’s phenotype and investigate his ancestry and what might distinguish him from modern dogs. RESULTS Balto shares just part of his diverse ancestry with the eponymous Siberian husky breed and was more genetically diverse than both modern breeds and working sled dogs. Both Balto and working sled dogs had a lower burden of rare, potentially damaging variation than modern breeds and fewer potentially damaging variants, suggesting that they represent genetically healthier populations. We inferred Balto’s appearance on the basis of genomic variants known to shape physical characteristics in dogs today. We found that Balto had a combination of coat features atypical for modern sled dog breeds and a slightly smaller stature, inferences that are confirmed by comparison to historical photographs. Balto’s ability to digest starch was enhanced compared to wolves and Greenland sled dogs but reduced compared to modern breeds. He carried a compendium of derived homozygous coding variants at constrained positions in genes connected to bone and skin development, which may have conferred a functional advantage. CONCLUSION Balto belonged to a population of small, fast, and fit sled dogs imported from Siberia. By sequencing his genome from his taxidermied remains and analyzing these data in the context of large comparative and canine datasets, we show that Balto and his working sled dog contemporaries were more genetically diverse than modern breeds and may have carried variants that helped them survive the harsh conditions of 1920s Alaska. Although the era of Balto and his contemporaries has passed, comparative genomics, supported by a growing collection of modern and past genomes, can provide insights into the selective pressures that shaped them. Balto, famed 20th-century Alaskan sled dog, shares common ancestry with modern Asian and Arctic canine lineages. In an unsupervised admixture analysis, Balto’s ancestry, representing 20th-century Alaskan sled dogs, is assigned predominantly to four Arctic lineage dog populations. He had no discernable wolf ancestry. The Alaskan sled dogs (a working population) did not fall into a distinct ancestry cluster but shared about a third of their ancestry with Balto in the supervised admixture analysis. Balto and working sled dogs carried fewer constrained and missense rare variants than modern dog breeds. IMAGE CREDIT: K. MORRILL
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    University of Chicago Press ; 2020
    In:  Physiological and Biochemical Zoology Vol. 93, No. 3 ( 2020-05), p. 199-209
    In: Physiological and Biochemical Zoology, University of Chicago Press, Vol. 93, No. 3 ( 2020-05), p. 199-209
    Type of Medium: Online Resource
    ISSN: 1522-2152 , 1537-5293
    Language: English
    Publisher: University of Chicago Press
    Publication Date: 2020
    detail.hit.zdb_id: 1465557-3
    detail.hit.zdb_id: 1473845-4
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    The Company of Biologists ; 2014
    In:  Journal of Experimental Biology Vol. 217, No. 3 ( 2014-02-01), p. 314-314
    In: Journal of Experimental Biology, The Company of Biologists, Vol. 217, No. 3 ( 2014-02-01), p. 314-314
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2014
    detail.hit.zdb_id: 1413561-9
    detail.hit.zdb_id: 1482461-9
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Online Resource
    Online Resource
    Informa UK Limited ; 2022
    In:  African Zoology Vol. 57, No. 1 ( 2022-01-02), p. iii-iv
    In: African Zoology, Informa UK Limited, Vol. 57, No. 1 ( 2022-01-02), p. iii-iv
    Type of Medium: Online Resource
    ISSN: 1562-7020 , 2224-073X
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2022
    detail.hit.zdb_id: 2018752-X
    detail.hit.zdb_id: 2070936-5
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2016
    In:  Climate Change Responses Vol. 3, No. 1 ( 2016-12)
    In: Climate Change Responses, Springer Science and Business Media LLC, Vol. 3, No. 1 ( 2016-12)
    Type of Medium: Online Resource
    ISSN: 2053-7565
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2016
    detail.hit.zdb_id: 2806583-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Online Resource
    Online Resource
    Frontiers Media SA ; 2020
    In:  Frontiers in Ecology and Evolution Vol. 8 ( 2020-3-31)
    In: Frontiers in Ecology and Evolution, Frontiers Media SA, Vol. 8 ( 2020-3-31)
    Type of Medium: Online Resource
    ISSN: 2296-701X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2020
    detail.hit.zdb_id: 2745634-1
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6643 ( 2023-04-28)
    Abstract: An estimated 160 million years have passed since the first placental mammals evolved. These eutherians are categorized into 19 orders consisting of nearly 4000 extant species, with ~70% being bats or rodents. Broad, in-depth, and comparative genomic studies across Eutheria have previously been unachievable because of the lack of genomic resources. The collaboration of the Zoonomia Consortium made available hundreds of high-quality genome assemblies for comparative analysis. Our focus within the consortium was to investigate the evolution of transposable elements (TEs) among placental mammals. Using these data, we identified previously known TEs, described previously unknown TEs, and analyzed the TE distribution among multiple taxonomic levels. RATIONALE The emergence of accurate and affordable sequencing technology has propelled efforts to sequence increasingly more nonmodel mammalian genomes in the past decade. Most of these efforts have traditionally focused on genic regions searching for patterns of selection or variation in gene regulation. The common trend of ignoring or trivializing TE annotation with newly published genomes has resulted in severe lag of TE analyses, leading to extensive undiscovered TE variation. This oversight has neglected an important source of evolution because the accumulation of TEs is attributable to drastic alterations in genome architecture, including insertions, deletions, duplications, translocations, and inversions. Our approach to the Zoonomia dataset was to provide future inquirers accurate and meticulous TE curations and to describe taxonomic variation among eutherians. RESULTS We annotated the TE content of 248 mammalian genome assemblies, which yielded a library of 25,676 consensus TE sequences, 8263 of which were previously unidentified TE sequences (available at https://dfam.org ). We affirmed that the largest component of a typical mammalian genome is comprised of TEs (average 45.6%). Of the 248 assemblies, the lowest genomic percentage of TEs was found in the star-nosed mole (27.6%), and the largest percentage was seen in the aardvark (74.5%), whose increase in TE accumulation drove a corresponding increase in genome size—a correlation we observed across Eutheria. The overall genomic proportions of recently accumulated TEs were roughly similar across most mammals in the dataset, with a few notable exceptions (see the figure). Diversity of recently accumulated TEs is highest among multiple families of bats, mostly driven by substantial DNA transposon activity. Our data also exhibit an increase of recently accumulated DNA transposons among carnivore lineages over their herbivorous counterparts, which suggests that diet may play a role in determining the genomic content of TEs. CONCLUSION The copious TE data provided in this work emanated from the largest comprehensive TE curation effort to date. Considering the wide-ranging effects that TEs impose on genomic architecture, these data are an important resource for future inquiries into mammalian genomics and evolution and suggest avenues for continued study of these important yet understudied genomic denizens. Boxplots depicting the range of recently accumulated TEs among mammals (by proportion of genome). Five categories of TE were examined: DNA transposons, long interspersed elements (LINEs), long terminal repeat (LTR) retrotransposons, rolling circle (RC) transposons, and short interspersed elements (SINEs). Species with the highest and lowest proportions for each TE type are indicated by a picture of the organism and its common name. With regard to RC and DNA transposons, we found that most mammalian genome assemblies exhibit essentially zero recent accumulation (RC: 240 of 248 mammals had 〈 0.1%; DNA: 210 of 248 mammals had 〈 0.1%). ILLUSTRATIONS: BRITTANY ANN HALE
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...