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  • 1
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2019
    In:  Proceedings of the National Academy of Sciences Vol. 116, No. 27 ( 2019-07-02), p. 13404-13413
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 116, No. 27 ( 2019-07-02), p. 13404-13413
    Abstract: BRUCE/Apollon is a membrane-associated inhibitor of apoptosis protein that is essential for viability and has ubiquitin-conjugating activity. On initiation of apoptosis, the ubiquitin ligase Nrdp1/RNF41 promotes proteasomal degradation of BRUCE. Here we demonstrate that BRUCE together with the proteasome activator PA28γ causes proteasomal degradation of LC3-I and thus inhibits autophagy. LC3-I on the phagophore membrane is conjugated to phosphatidylethanolamine to form LC3-II, which is required for the formation of autophagosomes and selective recruitment of substrates. SIP/CacyBP is a ubiquitination-related protein that is highly expressed in neurons and various tumors. Under normal conditions, SIP inhibits the ubiquitination and degradation of BRUCE, probably by blocking the binding of Nrdp1 to BRUCE. On DNA damage by topoisomerase inhibitors, Nrdp1 causes monoubiquitination of SIP and thus promotes apoptosis. However, on starvation, SIP together with Rab8 enhances the translocation of BRUCE into the recycling endosome, formation of autophagosomes, and degradation of BRUCE by optineurin-mediated autophagy. Accordingly, deletion of SIP in cultured cells reduces the autophagic degradation of damaged mitochondria and cytosolic protein aggregates. Thus, by stimulating proteasomal degradation of LC3-I, BRUCE also inhibits autophagy. Conversely, SIP promotes autophagy by blocking BRUCE-dependent degradation of LC3-I and by enhancing autophagosome formation and autophagic destruction of BRUCE. These actions of BRUCE and SIP represent mechanisms that link the regulation of autophagy and apoptosis under different conditions.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2019
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  • 2
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2023
    In:  Science Vol. 380, No. 6648 ( 2023-06-02), p. 913-924
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6648 ( 2023-06-02), p. 913-924
    Abstract: Comparative analysis of primate genomes within a phylogenetic context is essential for understanding the evolution of human genetic architecture and primate diversity. We present such a study of 50 primate species spanning 38 genera and 14 families, including 27 genomes first reported here, with many from previously less well represented groups, the New World monkeys and the Strepsirrhini. Our analyses reveal heterogeneous rates of genomic rearrangement and gene evolution across primate lineages. Thousands of genes under positive selection in different lineages play roles in the nervous, skeletal, and digestive systems and may have contributed to primate innovations and adaptations. Our study reveals that many key genomic innovations occurred in the Simiiformes ancestral node and may have had an impact on the adaptive radiation of the Simiiformes and human evolution.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
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  • 3
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 35, No. 6 ( 2015-02-11), p. 2674-2688
    Abstract: Microglia are the resident immune cells in the CNS and play diverse roles in the maintenance of CNS homeostasis. Recent studies have shown that microglia continually survey the CNS microenvironment and scavenge cell debris and aberrant proteins by phagocytosis and pinocytosis, and that reactive microglia are capable to present antigens to T cells and initiate immune responses. However, how microglia process the endocytosed contents and evoke an immune response remain unclear. Here we report that a size-dependent selective transport of small soluble contents from the pinosomal lumen into lysosomes is critical for the antigen processing in microglia. Using fluorescent probes and water-soluble magnetic nanobeads of defined sizes, we showed in cultured rodent microglia, and in a cell-free reconstructed system that pinocytosed proteins become degraded immediately following pinocytosis and the resulting peptides are selectively delivered to major histocompatibility complex class II (MHC-II) containing lysosomes, whereas undegraded proteins are retained in the pinosomal lumen. This early size-based sorting of pinosomal contents relied on the formation of transient tunnel between pinosomes and lysosomes in a Rab7- and dynamin II-dependent manner, which allowed the small contents to pass through but restricted large ones. Inhibition of the size-based sorting markedly reduced proliferation and cytokine release of cocultured CD4 + T cells, indicating that the size-based sorting is required for efficient antigen presentation by microglial cells. Together, these findings reveal a novel early sorting mechanism for pinosomal luminal contents in microglial cells, which may explain how microglia efficiently process protein antigens and evoke an immune response.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2015
    detail.hit.zdb_id: 1475274-8
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  • 4
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2014
    In:  Proceedings of the National Academy of Sciences Vol. 111, No. 52 ( 2014-12-30), p. 18501-18506
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 111, No. 52 ( 2014-12-30), p. 18501-18506
    Abstract: In high-temperature cuprate superconductors, it is now generally agreed that superconductivity is realized by doping an antiferromagnetic Mott (charge transfer) insulator. The doping-induced insulator-to-superconductor transition has been widely observed in cuprates, which provides important information for understanding the superconductivity mechanism. In the iron-based superconductors, however, the parent compound is mostly antiferromagnetic bad metal, raising a debate on whether an appropriate starting point should go with an itinerant picture or a localized picture. No evidence of doping-induced insulator–superconductor transition (or crossover) has been reported in the iron-based compounds so far. Here, we report an electronic evidence of an insulator–superconductor crossover observed in the single-layer FeSe film grown on a SrTiO 3 substrate. By taking angle-resolved photoemission measurements on the electronic structure and energy gap, we have identified a clear evolution of an insulator to a superconductor with increasing carrier concentration. In particular, the insulator–superconductor crossover in FeSe/SrTiO 3 film exhibits similar behaviors to that observed in the cuprate superconductors. Our results suggest that the observed insulator–superconductor crossover may be associated with the two-dimensionality that enhances electron localization or correlation. The reduced dimensionality and the interfacial effect provide a new pathway in searching for new phenomena and novel superconductors with a high transition temperature.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2014
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  • 5
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2023
    In:  Science Vol. 380, No. 6648 ( 2023-06-02)
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6648 ( 2023-06-02)
    Abstract: Hybridization is increasingly recognized as an important evolutionary force for generating species and phenotypic diversity in plants and animals. This is especially common in lineages that can tolerate whole-genome duplication and increased levels of ploidy. However, the role of hybridization in generating species and phenotypic diversity of lineages without polyploidization is underappreciated, especially in nonhominoid mammals. RATIONALE The snub-nosed monkey genus Rhinopithecus comprises five allopatric and morphologically differentiated species, the black-white snub-nosed monkey Rhinopithecus bieti , the black snub-nosed monkey Rhinopithecus strykeri , the golden snub-nosed monkey Rhinopithecus roxellana , the gray snub-nosed monkey Rhinopithecus brelichi , and the Tonkin snub-nosed monkey Rhinopithecus avunculus . They possess the same chromosome number, and it has been speculated that they have hybridized in the past. To examine the speciation histories of these species, we generated a chromosome-level high-quality reference genome assembly for the black-white snub-nosed monkey and analyzed 106 resequenced genomes of individuals from all five species. We conducted multiple population genomic analyses—including ADMIXTURE, D-statistics, phylogenetic reconstruction, and evolutionary scenario simulations—to investigate the genomic admixture of these species. We further applied genomic selective scans and functional assays to reveal the likely genetic basis of mosaic coat coloration of the hybrid species. Possible mechanisms of premating and postmating reproductive isolation barriers between the hybrid species and its parents are briefly discussed. RESULTS We show that historical hybridization directly resulted in the origin of the gray snub-nosed monkey. Population genomic analyses provided evidence for apparent genomic admixture across genomes of all gray snub-nosed monkeys from two parental lineages, the golden snub-nosed monkey and an ancestor of the black-white/black snub-nosed monkeys, with the majority of genome derived from the golden snub-nosed monkey. As a result of hybridization, the hybrid species possesses a mosaic of the color patterns of its parents. Genomic selection scans and functional assays identify several key melanogenesis-related genes ( PAH , APC , SLC45A 2, MYO7A , and ELOVL 4). Alleles of these genes were alternately inherited from each parent, likely producing the mosaic coat coloration of the hybrid monkey and promoting premating reproductive isolation of the hybrid species from both parents. In addition, alternate inheritance of divergent alleles at many loci, especially those involved in genetic incompatibility between the parents, may have contributed to postmating reproductive isolation of the gray snub-nosed monkey. CONCLUSION We report a notable example of hybrid speciation in primates and present a detailed evolutionary scenario from the genomic admixture to the likely reproductive isolation establishment owing to alternate inheritance of divergent alleles from parents. This study highlights the underappreciated role of interspecific hybridization in species and phenotypic diversity in mammals. The hybrid origin and genetic basis of mosaic coat coloration for the gray snub-nosed monkey. Interspecific hybridization between the golden snub-nosed monkey and the ancestor of black-white/black snub-nosed monkeys led to the genomic admixture of the gray snub-nosed monkey. Alleles of positively selected genes related to melanogenesis were alternately inherited from parental lineages A and B and contributed to the mosaic coat coloration of the hybrid species.
    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
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    detail.hit.zdb_id: 2066996-3
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    SSG: 11
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  • 6
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2004
    In:  Science Vol. 304, No. 5676 ( 2004-06-04), p. 1500-1502
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 304, No. 5676 ( 2004-06-04), p. 1500-1502
    Abstract: Caspases play a central role in apoptosis, a well-studied pathway of programmed cell death. Other programs of death potentially involving necrosis and autophagy may exist, but their relation to apoptosis and mechanisms of regulation remains unclear. We define a new molecular pathway in which activation of the receptor-interacting protein (a serine-threonine kinase) and Jun amino-terminal kinase induced cell death with the morphology of autophagy. Autophagic death required the genes ATG7 and beclin 1 and was induced by caspase-8 inhibition. Clinical therapies involving caspase inhibitors may arrest apoptosis but also have the unanticipated effect of promoting autophagic cell death.
    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: 2004
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  • 7
    Online Resource
    Online Resource
    Elsevier BV ; 2016
    In:  Information Sciences Vol. 370-371 ( 2016-11), p. 695-707
    In: Information Sciences, Elsevier BV, Vol. 370-371 ( 2016-11), p. 695-707
    Type of Medium: Online Resource
    ISSN: 0020-0255
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    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
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    detail.hit.zdb_id: 1478990-5
    SSG: 24,1
    SSG: 7,11
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  • 8
    In: Information Sciences, Elsevier BV, Vol. 372 ( 2016-12), p. 579-590
    Type of Medium: Online Resource
    ISSN: 0020-0255
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
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    detail.hit.zdb_id: 1478990-5
    SSG: 24,1
    SSG: 7,11
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  • 9
    In: Europhysics Letters, IOP Publishing, Vol. 141, No. 3 ( 2023-02-01), p. 35001-
    Abstract: Optical vortices (OVs) carry the orbital angular momentum with arbitrary topological charges, which has excellent potential in optical communication, photonic integrated circuits, optical trapping, and so on. However, generating arbitrary orders of adjustable optical vortices remains to be solved. Here, we propose a single-layer metal porous metasurface operating in infrared band for generating vortex beams from first to fourth order based on the spin-orbit interactions (SOI). The optical vortices with integral 2 π phase are obtained through generating double geometric phase induced by structural element spin rotation. Furthermore, the new phenomenon of optical vortices emerging on the center has also been observed in our system, which is caused by the coupling of multi-channel same-order OVs. Our work possesses wide applications in optical communication, multiplex and demultiplex systems, optical capture devices, and communication coding.
    Type of Medium: Online Resource
    ISSN: 0295-5075 , 1286-4854
    Language: Unknown
    Publisher: IOP Publishing
    Publication Date: 2023
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    detail.hit.zdb_id: 165776-8
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  • 10
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2011
    In:  Proceedings of the National Academy of Sciences Vol. 108, No. 17 ( 2011-04-26)
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 108, No. 17 ( 2011-04-26)
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2011
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