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  1. Article ; Online: Global level of methylation in the sea lamprey (jawless vertebrate) genome is intermediate between invertebrate and jawed vertebrate genomes.

    Zhang, Zhao / Liu, Gangbiao / Zhou, Zhan / Su, Zhixi / Gu, Xun

    Journal of experimental zoology. Part B, Molecular and developmental evolution

    2024  

    Abstract: In eukaryotes, cytosine methylation is a primary heritable epigenetic modification of the genome that regulates many cellular processes. In invertebrate, methylated cytosine generally located on specific genomic elements (e.g., gene bodies and silenced ... ...

    Abstract In eukaryotes, cytosine methylation is a primary heritable epigenetic modification of the genome that regulates many cellular processes. In invertebrate, methylated cytosine generally located on specific genomic elements (e.g., gene bodies and silenced repetitive elements) to show a "mosaic" pattern. While in jawed vertebrate (teleost and tetrapod), highly methylated cytosine located genome-wide but only absence at regulatory regions (e.g., promoter and enhancer). Many studies imply that the evolution of DNA methylation reprogramming may have helped the transition from invertebrates to jawed vertebrates, but the detail remains largely elusive. In this study, we used the whole-genome bisulfite-sequencing technology to investigate the genome-wide methylation in three tissues (heart, muscle, and sperm) from the sea lamprey, an extant agnathan (jawless) vertebrate. Strikingly, we found that the methylation level of the sea lamprey is very similar to that in sea urchin (a deuterostome) and sea squirt (a chordate) invertebrates. In sum, the global pattern in sea lamprey is intermediate methylation level (around 30%), that is higher than methylation level in the genomes of pre-bilaterians and protostomes (1%-10%), but lower than methylation level appeared in jawed vertebrates (around 70%, teleost and tetrapod). We anticipate that, in addition to genetic dynamics such as genome duplications, epigenetic dynamics such as global methylation reprograming was also orchestrated toward the emergence and evolution of vertebrates.
    Language English
    Publishing date 2024-03-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2103823-5
    ISSN 1552-5015 ; 0022-104X ; 1552-5007
    ISSN (online) 1552-5015
    ISSN 0022-104X ; 1552-5007
    DOI 10.1002/jez.b.23250
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Anciently duplicated genes continuously recruited to heart expression in vertebrate evolution are associated with heart chamber increase.

    Zou, Yangyun / Yang, Jingwen / Zhou, Jingqi / Liu, Gangbiao / Shen, Libing / Zhou, Zhan / Su, Zhixi / Gu, Xun

    Journal of experimental zoology. Part B, Molecular and developmental evolution

    2024  Volume 342, Issue 2, Page(s) 106–114

    Abstract: Although gene/genome duplications in the early stage of vertebrates have been thought to provide major resources of raw genetic materials for evolutionary innovations, it is unclear whether they continuously contribute to the evolution of morphological ... ...

    Abstract Although gene/genome duplications in the early stage of vertebrates have been thought to provide major resources of raw genetic materials for evolutionary innovations, it is unclear whether they continuously contribute to the evolution of morphological complexity during the course of vertebrate evolution, such as the evolution from two heart chambers (fishes) to four heart chambers (mammals and birds). We addressed this issue by our heart RNA-Seq experiments combined with published data, using 13 vertebrates and one invertebrate (sea squirt, as an outgroup). Our evolutionary transcriptome analysis showed that number of ancient paralogous genes expressed in heart tends to increase with the increase of heart chamber number along the vertebrate phylogeny, in spite that most of them were duplicated at the time near to the origin of vertebrates or even more ancient. Moreover, those paralogs expressed in heart exert considerably different functions from heart-expressed singletons: the former are functionally enriched in cardiac muscle and muscle contraction-related categories, whereas the latter play more basic functions of energy generation like aerobic respiration. These findings together support the notion that recruiting anciently paralogous genes that are expressed in heart is associated with the increase of chamber number in vertebrate evolution.
    MeSH term(s) Animals ; Evolution, Molecular ; Vertebrates/genetics ; Invertebrates/genetics ; Fishes/genetics ; Gene Duplication ; Phylogeny ; Multigene Family ; Mammals/genetics
    Language English
    Publishing date 2024-02-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2103823-5
    ISSN 1552-5015 ; 0022-104X ; 1552-5007
    ISSN (online) 1552-5015
    ISSN 0022-104X ; 1552-5007
    DOI 10.1002/jez.b.23248
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Age distribution patterns of human gene families: divergent for Gene Ontology categories and concordant between different subcellular localizations

    Liu, Gangbiao / Zou, Yangyun / Cheng, Qiqun / Zeng, Yanwu / Gu, Xun / Su, Zhixi

    Molecular genetics and genomics. 2014 Apr., v. 289, no. 2

    2014  

    Abstract: The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show ... ...

    Abstract The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show dissimilar retention patterns after duplication. It is known that genes in some functional categories are highly duplicated in the early stage of vertebrate evolution. However, the correlations of the age distribution pattern of gene duplication between the different functional categories are still unknown. To investigate this issue, we developed a robust pipeline to date the gene duplication events in the human genome. We successfully estimated about three-quarters of the duplication events within the human genome, along with the age distribution pattern in each Gene Ontology (GO) slim category. We found that some GO slim categories show different distribution patterns when compared to the whole genome. Further hierarchical clustering of the GO slim functional categories enabled grouping into two main clusters. We found that human genes located in the duplicated copy number variant regions, whose duplicate genes have not been fixed in the human population, were mainly enriched in the groups with a high proportion of recently duplicated genes. Moreover, we used a phylogenetic tree-based method to date the age of duplications in three signaling-related gene superfamilies: transcription factors, protein kinases and G-protein coupled receptors. These superfamilies were expressed in different subcellular localizations. They showed a similar age distribution as the signaling-related GO slim categories. We also compared the differences between the age distributions of gene duplications in multiple subcellular localizations. We found that the distribution patterns of the major subcellular localizations were similar to that of the whole genome. This study revealed the whole picture of the evolution patterns of gene functional categories in the human genome.
    Keywords duplicate genes ; evolution ; gene duplication ; human population ; humans ; protein kinases ; transcription factors
    Language English
    Dates of publication 2014-04
    Size p. 137-147.
    Publishing place Springer-Verlag
    Document type Article
    ISSN 1617-4615
    DOI 10.1007/s00438-013-0799-8
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: The evolutionary panorama of organ-specifically expressed or repressed orthologous genes in nine vertebrate species.

    Shen, Libing / Liu, Gangbiao / Zou, Yangyun / Zhou, Zhan / Su, Zhixi / Gu, Xun

    PloS one

    2015  Volume 10, Issue 2, Page(s) e0116872

    Abstract: RNA sequencing (RNA-Seq) technology provides the detailed transcriptomic information for a biological sample. Using the RNA-Seq data of six organs from nine vertebrate species, we identified a number of organ-specifically expressed or repressed ... ...

    Abstract RNA sequencing (RNA-Seq) technology provides the detailed transcriptomic information for a biological sample. Using the RNA-Seq data of six organs from nine vertebrate species, we identified a number of organ-specifically expressed or repressed orthologous genes whose expression patterns are mostly conserved across nine species. Our analyses show the following results: (i) About 80% of these genes have a chordate or more ancient origin and more than half of them are the legacy of one or multiple rounds of large-scale gene duplication events. (ii) Their evolutionary rates are shaped by the organ in which they are expressed or repressed, e.g. the genes specially expressed in testis and liver generally evolve more than twice as fast as the ones specially expressed in brain and cerebellum. The organ-specific transcription factors were discriminated from these genes. The ChIP-seq data from the ENCODE project also revealed the transcription-related factors that might be involved in regulating human organ-specifically expressed or repressed genes. Some of them are shared by all six human organs. The comparison of ENCODE data with mouse/chicken ChIP-seq data proposes that organ-specifically expressed or repressed orthologous genes are regulated in various combinatorial fashions in different species, although their expression features are conserved among these species. We found that the duplication events in some gene families might help explain the quick organ/tissue divergence in vertebrate lineage. The phylogenetic analysis of testis-specifically expressed genes suggests that some of them are prone to develop new functions for other organs/tissues.
    MeSH term(s) Animals ; Conserved Sequence/genetics ; Evolution, Molecular ; Gene Expression Profiling ; Gene Silencing ; Humans ; Multigene Family/genetics ; Organ Specificity ; Sequence Analysis, DNA ; Sequence Homology, Nucleic Acid ; Transcription, Genetic/genetics ; Vertebrates/genetics
    Language English
    Publishing date 2015
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0116872
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Mutation-profile-based methods for understanding selection forces in cancer somatic mutations: a comparative analysis.

    Zhou, Zhan / Zou, Yangyun / Liu, Gangbiao / Zhou, Jingqi / Wu, Jingcheng / Zhao, Shimin / Su, Zhixi / Gu, Xun

    Oncotarget

    2017  Volume 8, Issue 35, Page(s) 58835–58846

    Abstract: Human genes exhibit different effects on fitness in cancer and normal cells. Here, we present an evolutionary approach to measure the selection pressure on human genes, using the well-known ratio of the nonsynonymous to synonymous substitution rate in ... ...

    Abstract Human genes exhibit different effects on fitness in cancer and normal cells. Here, we present an evolutionary approach to measure the selection pressure on human genes, using the well-known ratio of the nonsynonymous to synonymous substitution rate in both cancer genomes (
    Language English
    Publishing date 2017-08-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.19371
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Age distribution patterns of human gene families: divergent for Gene Ontology categories and concordant between different subcellular localizations.

    Liu, Gangbiao / Zou, Yangyun / Cheng, Qiqun / Zeng, Yanwu / Gu, Xun / Su, Zhixi

    Molecular genetics and genomics : MGG

    2013  Volume 289, Issue 2, Page(s) 137–147

    Abstract: The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show ... ...

    Abstract The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show dissimilar retention patterns after duplication. It is known that genes in some functional categories are highly duplicated in the early stage of vertebrate evolution. However, the correlations of the age distribution pattern of gene duplication between the different functional categories are still unknown. To investigate this issue, we developed a robust pipeline to date the gene duplication events in the human genome. We successfully estimated about three-quarters of the duplication events within the human genome, along with the age distribution pattern in each Gene Ontology (GO) slim category. We found that some GO slim categories show different distribution patterns when compared to the whole genome. Further hierarchical clustering of the GO slim functional categories enabled grouping into two main clusters. We found that human genes located in the duplicated copy number variant regions, whose duplicate genes have not been fixed in the human population, were mainly enriched in the groups with a high proportion of recently duplicated genes. Moreover, we used a phylogenetic tree-based method to date the age of duplications in three signaling-related gene superfamilies: transcription factors, protein kinases and G-protein coupled receptors. These superfamilies were expressed in different subcellular localizations. They showed a similar age distribution as the signaling-related GO slim categories. We also compared the differences between the age distributions of gene duplications in multiple subcellular localizations. We found that the distribution patterns of the major subcellular localizations were similar to that of the whole genome. This study revealed the whole picture of the evolution patterns of gene functional categories in the human genome.
    MeSH term(s) Age Distribution ; Evolution, Molecular ; Gene Duplication ; Gene Ontology ; Genes ; Genome, Human ; Humans ; Multigene Family ; Phylogeny ; Subcellular Fractions
    Language English
    Publishing date 2013-12-10
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2044817-X
    ISSN 1617-4623 ; 1617-4615
    ISSN (online) 1617-4623
    ISSN 1617-4615
    DOI 10.1007/s00438-013-0799-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Age distribution patterns of human gene families: divergent for Gene Ontology categories and concordant between different subcellular localizations

    Liu, Gangbiao / Zou, Yangyun / Cheng, Qiqun / Zeng, Yanwu / Gu, Xun / Su, Zhixi

    Molecular genetics and genomics

    Volume v. 289,, Issue no. 2

    Abstract: The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show ... ...

    Abstract The age distribution of gene duplication events within the human genome exhibits two waves of duplications along with an ancient component. However, because of functional constraint differences, genes in different functional categories might show dissimilar retention patterns after duplication. It is known that genes in some functional categories are highly duplicated in the early stage of vertebrate evolution. However, the correlations of the age distribution pattern of gene duplication between the different functional categories are still unknown. To investigate this issue, we developed a robust pipeline to date the gene duplication events in the human genome. We successfully estimated about three-quarters of the duplication events within the human genome, along with the age distribution pattern in each Gene Ontology (GO) slim category. We found that some GO slim categories show different distribution patterns when compared to the whole genome. Further hierarchical clustering of the GO slim functional categories enabled grouping into two main clusters. We found that human genes located in the duplicated copy number variant regions, whose duplicate genes have not been fixed in the human population, were mainly enriched in the groups with a high proportion of recently duplicated genes. Moreover, we used a phylogenetic tree-based method to date the age of duplications in three signaling-related gene superfamilies: transcription factors, protein kinases and G-protein coupled receptors. These superfamilies were expressed in different subcellular localizations. They showed a similar age distribution as the signaling-related GO slim categories. We also compared the differences between the age distributions of gene duplications in multiple subcellular localizations. We found that the distribution patterns of the major subcellular localizations were similar to that of the whole genome. This study revealed the whole picture of the evolution patterns of gene functional categories in the human genome.
    Keywords human population ; transcription factors ; duplicate genes ; protein kinases ; humans ; evolution ; gene duplication
    Language English
    Document type Article
    ISSN 1617-4615
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

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