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  • 1
    Online Resource
    Online Resource
    eLife Sciences Publications, Ltd ; 2017
    In:  eLife Vol. 6 ( 2017-09-12)
    In: eLife, eLife Sciences Publications, Ltd, Vol. 6 ( 2017-09-12)
    Abstract: Before birth, mammals in their mother’s womb are provided with nutrients and oxygen via an organ called the placenta. After birth, the mother produces milk to feed her young, which supports their continuing development. The majority of living mammals, from mice to humans, belong to a group known as “eutheria” and have placentas made up of many different types of cells and tissues. This complex placenta has caused many people to wrongly refer to this group as “the placental mammals”. However, marsupials like kangaroos and koalas represent a second group of mammals that also have a placenta, albeit a much simpler one that consists of only a few layers of cells. The simpler placenta means that marsupials give birth to young that are underdeveloped compared to eutherians. These young must develop further inside the mother’s pouch, where they are fed with milk that changes over time to support the different stages of their development. As a result, marsupials produce a more complicated range of milks than eutherians. To date, scientists do not fully understand how these two groups of mammals evolved to nurture their offspring in two different ways. Guernsey et al. have now studied which genes are active in the placenta and milk-producing “mammary” glands of the tammar wallaby, a small member of the kangaroo family. Comparing the data with similar data from mice and humans revealed that marsupial and eutherian placentas are alike in many ways. For example, both rapidly change which genes are active as the placenta matures, and both contain tissues that perform specific tasks such as providing offspring with nourishment for growth and oxygen for respiration. The analysis also shows that mammary glands in marsupials use similar genes to those used by the eutherian placenta to support the development of offspring. This suggests the placenta and the mammary gland have converged on a similar set of genes to allow female mammals to nourish their young. Overall, the findings further scientific knowledge about the evolution of pregnancy and milk production in marsupials, paving the way for further research into the diversity of life on Earth. The findings also confirm that marsupials have working placentas, stressing that eutherians and marsupials should both be referred to as “placental mammals”.
    Type of Medium: Online Resource
    ISSN: 2050-084X
    Language: English
    Publisher: eLife Sciences Publications, Ltd
    Publication Date: 2017
    detail.hit.zdb_id: 2687154-3
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  • 2
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2013
    In:  Science Vol. 342, No. 6160 ( 2013-11-15), p. 812-813
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 342, No. 6160 ( 2013-11-15), p. 812-813
    Abstract: It took more than three decades—and a Nobel Prize in 1983—for Barbara McClintock's discovery of transposition and mobile genetic elements to become widely accepted. However, her vision of transposons as “controlling elements” and architects of genome organization has remained controversial. On page 846 of this issue, a report by Ellison and Bachtrog brings McClintock's prescient ideas back to center stage ( 1 ). They show that transposition has shaped the regulatory landscape of an entire chromosome at least twice in the evolutionary history of Drosophila , facilitating the emergence of novel sex chromosomes.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2013
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    detail.hit.zdb_id: 2060783-0
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    The Royal Society ; 2020
    In:  Philosophical Transactions of the Royal Society B: Biological Sciences Vol. 375, No. 1795 ( 2020-03-30), p. 20190330-
    In: Philosophical Transactions of the Royal Society B: Biological Sciences, The Royal Society, Vol. 375, No. 1795 ( 2020-03-30), p. 20190330-
    Abstract: Transposons are mobile genetic elements that have made a large contribution to genome evolution in a largely species-specific manner. A wide variety of different transposons have invaded genomes throughout evolution, acting in a first instance as ‘selfish’ elements, whose success was determined by their ability to self-replicate and expand within the host genome. However, their coevolution with the host has created many crossroads between transposons and the regulation of host gene expression. Transposons are an abundant source of transcriptional modulatory elements, such as gene promoters and enhancers, splicing and termination sites, and regulatory non-coding RNAs. Moreover, transposons have driven the evolution of host defence mechanisms that have been repurposed for gene regulation. However, dissecting the potential functional roles of transposons remains challenging owing to their evolutionary path, as well as their repetitive nature, which requires the development of specialized analytical tools. In this special issue, we present a collection of articles that lay out current paradigms in the field and discuss a vision for future research. This article is part of a discussion meeting issue ‘Crossroads between transposons and gene regulation’.
    Type of Medium: Online Resource
    ISSN: 0962-8436 , 1471-2970
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    Language: English
    Publisher: The Royal Society
    Publication Date: 2020
    detail.hit.zdb_id: 1462620-2
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  • 4
    In: Genome Research, Cold Spring Harbor Laboratory, Vol. 32, No. 6 ( 2022-06), p. 1058-1073
    Abstract: Understanding how regulatory mechanisms evolve is critical for understanding the processes that give rise to novel phenotypes. Snake venom systems represent a valuable and tractable model for testing hypotheses related to the evolution of novel regulatory networks, yet the regulatory mechanisms underlying venom production remain poorly understood. Here, we use functional genomics approaches to investigate venom regulatory architecture in the prairie rattlesnake and identify cis -regulatory sequences (enhancers and promoters), trans -regulatory transcription factors, and integrated signaling cascades involved in the regulation of snake venom genes. We find evidence that two conserved vertebrate pathways, the extracellular signal-regulated kinase and unfolded protein response pathways, were co-opted to regulate snake venom. In one large venom gene family (snake venom serine proteases), this co-option was likely facilitated by the activity of transposable elements. Patterns of snake venom gene enhancer conservation, in some cases spanning 50 million yr of lineage divergence, highlight early origins and subsequent lineage-specific adaptations that have accompanied the evolution of venom regulatory architecture. We also identify features of chromatin structure involved in venom regulation, including topologically associated domains and CTCF loops that underscore the potential importance of novel chromatin structure to coevolve when duplicated genes evolve new regulatory control. Our findings provide a model for understanding how novel regulatory systems may evolve through a combination of genomic processes, including tandem duplication of genes and regulatory sequences, cis -regulatory sequence seeding by transposable elements, and diverse transcriptional regulatory proteins controlled by a co-opted regulatory cascade.
    Type of Medium: Online Resource
    ISSN: 1088-9051 , 1549-5469
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    Language: English
    Publisher: Cold Spring Harbor Laboratory
    Publication Date: 2022
    detail.hit.zdb_id: 1483456-X
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  • 5
    Online Resource
    Online Resource
    eLife Sciences Publications, Ltd ; 2023
    In:  eLife Vol. 12 ( 2023-05-09)
    In: eLife, eLife Sciences Publications, Ltd, Vol. 12 ( 2023-05-09)
    Abstract: Regulatory networks underlying innate immunity continually face selective pressures to adapt to new and evolving pathogens. Transposable elements (TEs) can affect immune gene expression as a source of inducible regulatory elements, but the significance of these elements in facilitating evolutionary diversification of innate immunity remains largely unexplored. Here, we investigated the mouse epigenomic response to type II interferon (IFN) signaling and discovered that elements from a subfamily of B2 SINE (B2_Mm2) contain STAT1 binding sites and function as IFN-inducible enhancers. CRISPR deletion experiments in mouse cells demonstrated that a B2_Mm2 element has been co-opted as an enhancer driving IFN-inducible expression of Dicer1 . The rodent-specific B2 SINE family is highly abundant in the mouse genome and elements have been previously characterized to exhibit promoter, insulator, and non-coding RNA activity. Our work establishes a new role for B2 elements as inducible enhancer elements that influence mouse immunity, and exemplifies how lineage-specific TEs can facilitate evolutionary turnover and divergence of innate immune regulatory networks.
    Type of Medium: Online Resource
    ISSN: 2050-084X
    Language: English
    Publisher: eLife Sciences Publications, Ltd
    Publication Date: 2023
    detail.hit.zdb_id: 2687154-3
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  • 6
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2013
    In:  Nature Genetics Vol. 45, No. 3 ( 2013-3), p. 325-329
    In: Nature Genetics, Springer Science and Business Media LLC, Vol. 45, No. 3 ( 2013-3), p. 325-329
    Type of Medium: Online Resource
    ISSN: 1061-4036 , 1546-1718
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    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2013
    detail.hit.zdb_id: 1494946-5
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  • 7
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 1506, No. 1 ( 2021-12), p. 118-141
    Abstract: The human transcriptome contains many types of noncoding RNAs, which rival the number of protein‐coding species. From long noncoding RNAs (lncRNAs) that are over 200 nucleotides long to piwi‐interacting RNAs (piRNAs) of only 20 nucleotides, noncoding RNAs play important roles in regulating transcription, epigenetic modifications, translation, and cell signaling. Roles for noncoding RNAs in disease mechanisms are also being uncovered, and several species have been identified as potential drug targets. On May 11–14, 2021, the Keystone eSymposium “Noncoding RNAs: Biology and Applications” brought together researchers working in RNA biology, structure, and technologies to accelerate both the understanding of RNA basic biology and the translation of those findings into clinical applications.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
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    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2834079-6
    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
    SSG: 11
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  • 8
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2016
    In:  Science Vol. 351, No. 6277 ( 2016-03-04), p. 1083-1087
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 351, No. 6277 ( 2016-03-04), p. 1083-1087
    Abstract: Endogenous retroviruses (ERVs) are abundant in mammalian genomes and contain sequences modulating transcription. The impact of ERV propagation on the evolution of gene regulation remains poorly understood. We found that ERVs have shaped the evolution of a transcriptional network underlying the interferon (IFN) response, a major branch of innate immunity, and that lineage-specific ERVs have dispersed numerous IFN-inducible enhancers independently in diverse mammalian genomes. CRISPR-Cas9 deletion of a subset of these ERV elements in the human genome impaired expression of adjacent IFN-induced genes and revealed their involvement in the regulation of essential immune functions, including activation of the AIM2 inflammasome. Although these regulatory sequences likely arose in ancient viruses, they now constitute a dynamic reservoir of IFN-inducible enhancers fueling genetic innovation in mammalian immune defenses.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2016
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    detail.hit.zdb_id: 2060783-0
    SSG: 11
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2013
    In:  BioEssays Vol. 35, No. 10 ( 2013-10), p. 853-861
    In: BioEssays, Wiley, Vol. 35, No. 10 ( 2013-10), p. 853-861
    Abstract: The mammalian placenta exhibits elevated expression of endogenous retroviruses (ERVs), but the evolutionary significance of this feature remains unclear. I propose that ERV‐mediated regulatory evolution was, and continues to be, an important mechanism underlying the evolution of placental development. Many recent studies have focused on the co‐option of ERV‐derived genes for specific functional adaptations in the placenta. However, the co‐option of ERV‐derived regulatory elements could potentially lead to the incorporation of entire gene regulatory networks, which, I argue, would facilitate relatively rapid developmental evolution of the placenta. I suggest a model in which an ancient retroviral infection led to the establishment of the ancestral placental developmental gene network through the co‐option of ERV‐derived regulatory elements. Consequently, placental development would require elevated tolerance to ERV activity. This in turn would expose a continuous stream of novel ERV mutations that may have catalyzed the developmental diversification of the mammalian placenta.
    Type of Medium: Online Resource
    ISSN: 0265-9247 , 1521-1878
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2013
    detail.hit.zdb_id: 1473795-4
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2008
    In:  Genetics Vol. 179, No. 4 ( 2008-08-01), p. 2075-2089
    In: Genetics, Oxford University Press (OUP), Vol. 179, No. 4 ( 2008-08-01), p. 2075-2089
    Abstract: Genes expressed in testes are critical to male reproductive success, affecting spermatogenesis, sperm competition, and sperm–egg interaction. Comparing the evolution of testis proteins at different taxonomic levels can reveal which genes and functional classes are targets of natural and sexual selection and whether the same genes are targets among taxa. Here we examine the evolution of testis-expressed proteins at different levels of divergence among three rodents, mouse (Mus musculus), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly evolving genes. Comparison of expressed sequence tags (ESTs) from testes suggests that proteins with testis-specific expression evolve more rapidly on average than proteins with maximal expression in other tissues. Genes with the highest rates of evolution have a variety of functional roles including signal transduction, DNA binding, and egg–sperm interaction. Most of these rapidly evolving genes have not been identified previously as targets of selection in comparisons among more divergent mammals. To determine if these genes are evolving rapidly among closely related species, we sequenced 11 of these genes in six Peromyscus species and found evidence for positive selection in five of them. Together, these results demonstrate rapid evolution of functionally diverse testis-expressed proteins in rodents, including the identification of amino acids under lineage-specific selection in Peromyscus. Evidence for positive selection among closely related species suggests that changes in these proteins may have consequences for reproductive isolation.
    Type of Medium: Online Resource
    ISSN: 1943-2631
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2008
    detail.hit.zdb_id: 1477228-0
    SSG: 12
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