Maternally recruited Aurora C kinase is more stable than Aurora B to support mouse oocyte maturation and early development - Wikidata - awgldk - TriplyDB

Maternally recruited Aurora C kinase is more stable than Aurora B to support mouse oocyte maturation and early development

Maternally recruited Aurora C kinase is more stable than Aurora B to support mouse oocyte maturation and early development

http://www.wikidata.org/entity/Q36170725

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Functions of Aurora kinase C in meiosis and cancer Possible Role of Aurora-C in Meiosis Cell division: control of the chromosomal passenger complex in time and space Selective disruption of aurora C kinase reveals distinct functions from aurora B kinase during meiosis in mouse oocytes Phosphorylation of threonine 3 on histone H3 by haspin kinase is required for meiosis I in mouse oocytes Aurora-C Interactions with Survivin and INCENP Reveal Shared and Distinct Features Compared with Aurora-B Chromosome Passenger Protein Complex Survivin is essential for fertile egg production and female fertility in mice Zwint-1 is required for spindle assembly checkpoint function and kinetochore-microtubule attachment during oocyte meiosis.Reduced ability to recover from spindle disruption and loss of kinetochore spindle assembly checkpoint proteins in oocytes from aged mice.The impact of vitrification on murine germinal vesicle oocyte In vitro maturation and aurora kinase A protein expression.Mouse oocytes depend on BubR1 for proper chromosome segregation but not for prophase I arrest Expression and characterization of three Aurora kinase C splice variants found in human oocytes P-TEFb Kinase Activity Is Essential for Global Transcription, Resumption of Meiosis and Embryonic Genome Activation in Pig.Aurora kinase A drives MTOC biogenesis but does not trigger resumption of meiosis in mouse oocytes matured in vivo.H3 Thr3 phosphorylation is crucial for meiotic resumption and anaphase onset in oocyte meiosis.Digital multiplexed mRNA analysis of functionally important genes in single human oocytes and correlation of changes in transcript levels with oocyte protein expression.Overexpression of Aurora-C interferes with the spindle checkpoint by promoting the degradation of Aurora-B.Maternal obesity is associated with ovarian inflammation and upregulation of early growth response factor 1.Haspin inhibition reveals functional differences of interchromatid axis-localized AURKB and AURKC.Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.Late mitotic functions of Aurora kinases.Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy.The chromosomal basis of meiotic acentrosomal spindle assembly and function in oocytes.Specialize and Divide (Twice): Functions of Three Aurora Kinase Homologs in Mammalian Oocyte Meiotic Maturation.Haspin kinase regulates microtubule-organizing center clustering and stability through Aurora kinase C in mouse oocytes.Inhibition of P-TEFb disrupts global transcription, oocyte maturation, and embryo development in the mouse.Differential regulation of H3S10 phosphorylation, mitosis progression and cell fate by Aurora Kinase B and C in mouse preimplantation embryos.Reduced chromosome cohesion measured by interkinetochore distance is associated with aneuploidy even in oocytes from young mice.Knockdown of RBBP7 unveils a requirement of histone deacetylation for CPC function in mouse oocytes.Regulation of chromosome segregation in oocytes and the cellular basis for female meiotic errors.Maternal RNA regulates Aurora C kinase during mouse oocyte maturation in a translation-independent fashion.DNA damage induces a kinetochore-based ATM/ATR-independent SAC arrest unique to the first meiotic division in mouse oocytes.Meiotic Divisions: No Place for Gender Equality.Multiple Duties for Spindle Assembly Checkpoint Kinases in Meiosis.Characterization of macrozoospermia-associated AURKC mutations in a mammalian meiotic system.Non-canonical function of spindle assembly checkpoint proteins after APC activation reduces aneuploidy in mouse oocytes.Chromosome segregation regulation in human zygotes: altered mitotic histone phosphorylation dynamics underlying centromeric targeting of the chromosomal passenger complex.Toll-like receptor 3 regulates cord blood-derived endothelial cell function in vitro and in vivo.The functional diversity of Aurora kinases: a comprehensive review

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P2860

Maternally recruited Aurora C kinase is more stable than Aurora B to support mouse oocyte maturation and early development

http://www.wikidata.org/entity/Q36170725

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Maternally recruited Aurora C ...... turation and early development

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Maternally recruited Aurora C ...... turation and early development

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Maternally recruited Aurora C ...... turation and early development

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Karen Schindler

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Michael A Lampson

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Richard M Schultz

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P2860

Cloning and characterization of a novel human Aurora C splicing variant

The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint

The maternal-effect gene cellular island encodes aurora B kinase and is essential for furrow formation in the early zebrafish embryo

Drosophila aurora B kinase is required for histone H3 phosphorylation and condensin recruitment during chromosome condensation and to organize the central spindle during cytokinesis

Protein kinase profile of sperm and eggs: cloning and characterization of two novel testis-specific protein kinases (AIE1, AIE2) related to yeast and fly chromosome segregation regulators

Protein tyrosine kinase Wee1B is essential for metaphase II exit in mouse oocytes

Recruitment of Orc6l, a dormant maternal mRNA in mouse oocytes, is essential for DNA replication in 1-cell embryos

A novel mammalian, mitotic spindle-associated kinase is related to yeast and fly chromosome segregation regulators

Genome-wide analysis of translation reveals a critical role for deleted in azoospermia-like (Dazl) at the oocyte-to-zygote transition

Aurora-C kinase deficiency causes cytokinesis failure in meiosis I and production of large polyploid oocytes in mice.

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