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Centromere drive and suppression by parallel pathways for recruiting microtubule destabilizers

https://doi.org/10.1101/2020.11.26.400515
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.10618openalex-snapshot
Distortion of female meiotic segregation and reduced male fertility in human Robertsonian translocations: Consistent with the centromere model of co‐evolving centromere DNA/centromeric histone (CENP‐A)
inferredcites →https://doi.org/10.1002/tcm.1770150502openalex-snapshot
Susceptibility to vinblastine‐induced aneuploidy and preferential chromosome segregation during meiosis I in Robertsonian heterozygous mice
inferredcites →https://doi.org/10.1006/dbio.1998.9005openalex-snapshot
Centromeric Protein B Null Mice Are Viable with No Apparent Abnormalities
inferredcites →https://doi.org/10.1007/s00294-017-0719-2openalex-snapshot
The 2 micron plasmid: a selfish genetic element with an optimized survival strategy within Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s004120050343openalex-snapshot
The cenpB gene is not essential in mice
inferredcites →https://doi.org/10.1007/s00439-016-1748-5openalex-snapshot
Regional selection of the brain size regulating gene CASC5 provides new insight into human brain evolution
inferredcites →https://doi.org/10.1016/j.cell.2007.10.045openalex-snapshot
CENP-B Controls Centromere Formation Depending on the Chromatin Context
inferredcites →https://doi.org/10.1016/j.cell.2009.02.039openalex-snapshot
Centromere-Specific Assembly of CENP-A Nucleosomes Is Mediated by HJURP
inferredcites →https://doi.org/10.1016/j.cell.2009.02.040openalex-snapshot
HJURP Is a Cell-Cycle-Dependent Maintenance and Deposition Factor of CENP-A at Centromeres
inferredcites →https://doi.org/10.1016/j.cell.2009.08.036openalex-snapshot
Major Evolutionary Transitions in Centromere Complexity
inferredcites →https://doi.org/10.1016/j.cell.2011.11.061openalex-snapshot
CENP-T-W-S-X Forms a Unique Centromeric Chromatin Structure with a Histone-like Fold
inferredcites →https://doi.org/10.1016/j.cell.2016.10.005openalex-snapshot
Structure of the MIS12 Complex and Molecular Basis of Its Interaction with CENP-C at Human Kinetochores
inferredcites →https://doi.org/10.1016/j.cell.2019.06.006openalex-snapshot
Human Artificial Chromosomes that Bypass Centromeric DNA
inferredcites →https://doi.org/10.1016/j.cell.2019.07.001openalex-snapshot
Molecular Strategies of Meiotic Cheating by Selfish Centromeres
inferredcites →https://doi.org/10.1016/j.celrep.2018.09.032openalex-snapshot
Microcephaly Modeling of Kinetochore Mutation Reveals a Brain-Specific Phenotype
inferredcites →https://doi.org/10.1016/j.cub.2013.11.046openalex-snapshot
KI Motifs of Human Knl1 Enhance Assembly of Comprehensive Spindle Checkpoint Complexes around MELT Repeats
inferredcites →https://doi.org/10.1016/j.cub.2014.08.017openalex-snapshot
Centromere Strength Provides the Cell Biological Basis for Meiotic Drive and Karyotype Evolution in Mice
inferredcites →https://doi.org/10.1016/j.cub.2015.01.059openalex-snapshot
Distinct Organization and Regulation of the Outer Kinetochore KMN Network Downstream of CENP-C and CENP-T
inferredcites →https://doi.org/10.1016/j.cub.2015.05.013openalex-snapshot
Spatial Regulation of Kinetochore Microtubule Attachments by Destabilization at Spindle Poles in Meiosis I
inferredcites →https://doi.org/10.1016/j.cub.2017.06.069openalex-snapshot
Expanded Satellite Repeats Amplify a Discrete CENP-A Nucleosome Assembly Site on Chromosomes that Drive in Female Meiosis
inferredcites →https://doi.org/10.1016/j.cub.2019.06.062openalex-snapshot
Structure of the Human Core Centromeric Nucleosome Complex
inferredcites →https://doi.org/10.1016/j.cub.2019.12.014openalex-snapshot
CenH3-Independent Kinetochore Assembly in Lepidoptera Requires CCAN, Including CENP-T
inferredcites →https://doi.org/10.1016/j.devcel.2006.11.002openalex-snapshot
Priming of Centromere for CENP-A Recruitment by Human hMis18α, hMis18β, and M18BP1
inferredcites →https://doi.org/10.1016/j.devcel.2015.03.020openalex-snapshot
DNA Sequence-Specific Binding of CENP-B Enhances the Fidelity of Human Centromere Function
inferredcites →https://doi.org/10.1016/j.devcel.2016.02.008openalex-snapshot
HP1-Assisted Aurora B Kinase Activity Prevents Chromosome Segregation Errors
inferredcites →https://doi.org/10.1016/j.devcel.2016.05.006openalex-snapshot
KAT7/HBO1/MYST2 Regulates CENP-A Chromatin Assembly by Antagonizing Suv39h1-Mediated Centromere Inactivation
inferredcites →https://doi.org/10.1016/j.devcel.2019.02.002openalex-snapshot
The Kinetochore-Microtubule Coupling Machinery Is Repurposed in Sensory Nervous System Morphogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2019.02.003openalex-snapshot
Kinetochore Proteins Have a Post-Mitotic Function in Neurodevelopment
inferredcites →https://doi.org/10.1016/j.molcel.2014.01.019openalex-snapshot
Modular Assembly of RWD Domains on the Mis12 Complex Underlies Outer Kinetochore Organization
inferredcites →https://doi.org/10.1016/j.molcel.2018.07.038openalex-snapshot
Reconstitution of a 26-Subunit Human Kinetochore Reveals Cooperative Microtubule Binding by CENP-OPQUR and NDC80
inferredcites →https://doi.org/10.1016/j.mrgentox.2013.05.011openalex-snapshot
New DNA probes to detect aneugenicity in rat bone marrow micronucleated cells by a pan-centromeric FISH analysis
inferredcites →https://doi.org/10.1016/j.tig.2017.07.011openalex-snapshot
Transposable Element Domestication As an Adaptation to Evolutionary Conflicts
inferredcites →https://doi.org/10.1016/j.tig.2017.08.006openalex-snapshot
The Role of KRAB-ZFPs in Transposable Element Repression and Mammalian Evolution
inferredcites →https://doi.org/10.1016/j.yexcr.2020.111959openalex-snapshot
From evolution to function: Two sides of the same CENP-B coin?
inferredcites →https://doi.org/10.1016/s0168-9525(97)01098-6openalex-snapshot
Centromeres, CENP-B and Tigger too
inferredcites →https://doi.org/10.1023/a:1018422325569openalex-snapshot
Characterization of internal DNA-binding and C-terminal dimerization domains of human centromere/kinetochore autoantigen CENP-C in vitro: role of DNA-binding and self-associating activities in kinetochore organization
inferredcites →https://doi.org/10.1038/nature02426openalex-snapshot
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
inferredcites →https://doi.org/10.1038/nature09390openalex-snapshot
Phosphorylation of the CPC by Cdk1 promotes chromosome bi-orientation
inferredcites →https://doi.org/10.1038/nature10413openalex-snapshot
Mouse genomic variation and its effect on phenotypes and gene regulation
inferredcites →https://doi.org/10.1038/nature14097openalex-snapshot
Meikin is a conserved regulator of meiosis-I-specific kinetochore function
inferredcites →https://doi.org/10.1038/nature19333openalex-snapshot
Insights from biochemical reconstitution into the architecture of human kinetochores
inferredcites →https://doi.org/10.1038/ncb2075openalex-snapshot
Human POGZ modulates dissociation of HP1α from mitotic chromosome arms through Aurora B activation
inferredcites →https://doi.org/10.1038/ncb2805openalex-snapshot
A two-step mechanism for epigenetic specification of centromere identity and function
inferredcites →https://doi.org/10.1038/nrg.2015.18openalex-snapshot
Causes of evolutionary rate variation among protein sites
inferredcites →https://doi.org/10.1038/nrg3905openalex-snapshot
Evolutionary insights into host–pathogen interactions from mammalian sequence data
inferredcites →https://doi.org/10.1038/nrm.2017.119openalex-snapshot
Ten principles of heterochromatin formation and function
inferredcites →https://doi.org/10.1038/nrm3916openalex-snapshot
Regulation of kinetochore–microtubule attachments through homeostatic control during mitosis
inferredcites →https://doi.org/10.1038/s41586-019-1609-1openalex-snapshot
Structure of the inner kinetochore CCAN complex assembled onto a centromeric nucleosome
inferredcites →https://doi.org/10.1073/pnas.0308637101openalex-snapshot
Human centromere repositioning “in progress”
inferredcites →https://doi.org/10.1083/jcb.109.5.1963openalex-snapshot
A human centromere antigen (CENP-B) interacts with a short specific sequence in alphoid DNA, a human centromeric satellite.
inferredcites →https://doi.org/10.1083/jcb.141.2.309openalex-snapshot
Centromere Protein B Null Mice are Mitotically and Meiotically Normal but Have Lower Body and Testis Weights
inferredcites →https://doi.org/10.1083/jcb.143.7.1763openalex-snapshot
INCENP Centromere and Spindle Targeting: Identification of Essential Conserved Motifs and Involvement of Heterochromatin Protein HP1
inferredcites →https://doi.org/10.1083/jcb.201106079openalex-snapshot
CENP-C recruits M18BP1 to centromeres to promote CENP-A chromatin assembly
inferredcites →https://doi.org/10.1083/jcb.201412028openalex-snapshot
CENP-C is a blueprint for constitutive centromere–associated network assembly within human kinetochores
inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/gbe/evv140openalex-snapshot
Widespread Recurrent Patterns of Rapid Repeat Evolution in the Kinetochore Scaffold KNL1
inferredcites →https://doi.org/10.1093/gbe/evx088openalex-snapshot
Unique Phylogenetic Distributions of the Ska and Dam1 Complexes Support Functional Analogy and Suggest Multiple Parallel Displacements of Ska by Dam1
inferredcites →https://doi.org/10.1093/genetics/157.3.1293openalex-snapshot
Adaptive Evolution of Cid, a Centromere-Specific Histone in Drosophila
inferredcites →https://doi.org/10.1093/humrep/der080openalex-snapshot
Meiotic segregation of Robertsonian translocations ascertained in cleavage-stage embryos--implications for preimplantation genetic diagnosis
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/msm221openalex-snapshot
Convergent Domestication of pogo-like Transposases into Centromere-Binding Proteins in Fission Yeast and Mammals
inferredcites →https://doi.org/10.1093/molbev/msq043openalex-snapshot
Adaptive Evolution of Foundation Kinetochore Proteins in Primates
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msv145openalex-snapshot
Duplication and Adaptive Evolution of a Key Centromeric Protein inMimulus, a Genus with Female Meiotic Drive
inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot
MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform
inferredcites →https://doi.org/10.1093/nar/gkx704openalex-snapshot
Genome-scale detection of positive selection in nine primates predicts human-virus evolutionary conflicts
inferredcites →https://doi.org/10.1101/gad.997702openalex-snapshot
Fission yeast CENP-B homologs nucleate centromeric heterochromatin by promoting heterochromatin-specific histone tail modifications
inferredcites →https://doi.org/10.1101/gr.234096.117openalex-snapshot
Repeat associated mechanisms of genome evolution and function revealed by the Mus caroli and Mus pahari genomes
inferredcites →https://doi.org/10.1101/sqb.2017.82.034298openalex-snapshot
Cellular and Molecular Mechanisms of Centromere Drive
inferredcites →https://doi.org/10.1126/science.1062939openalex-snapshot
The Centromere Paradox: Stable Inheritance with Rapidly Evolving DNA
inferredcites →https://doi.org/10.1126/science.1161406openalex-snapshot
Centromere-Associated Female Meiotic Drive Entails Male Fitness Costs in Monkeyflowers
inferredcites →https://doi.org/10.1126/science.1189435openalex-snapshot
Histone H3 Thr-3 Phosphorylation by Haspin Positions Aurora B at Centromeres in Mitosis
inferredcites →https://doi.org/10.1126/science.1189505openalex-snapshot
Survivin Reads Phosphorylated Histone H3 Threonine 3 to Activate the Mitotic Kinase Aurora B
inferredcites →https://doi.org/10.1126/science.1194498openalex-snapshot
Two Histone Marks Establish the Inner Centromere and Chromosome Bi-Orientation
inferredcites →https://doi.org/10.1126/science.1235532openalex-snapshot
A Conserved Mechanism for Centromeric Nucleosome Recognition by Centromere Protein CENP-C
inferredcites →https://doi.org/10.1126/science.aan0092openalex-snapshot
Spindle asymmetry drives non-Mendelian chromosome segregation
inferredcites →https://doi.org/10.1126/science.aav6202openalex-snapshot
Large-scale ruminant genome sequencing provides insights into their evolution and distinct traits
inferredcites →https://doi.org/10.1186/gb-2013-14-1-r10openalex-snapshot
Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
inferredcites →https://doi.org/10.1186/jbiol11openalex-snapshot
Adaptive evolution of centromere proteins in plants and animals
inferredcites →https://doi.org/10.1186/s13100-020-00220-0openalex-snapshot
Evolution of pogo, a separate superfamily of IS630-Tc1-mariner transposons, revealing recurrent domestication events in vertebrates
inferredcites →https://doi.org/10.1242/jcs.180786openalex-snapshot
CENP-C and CENP-I are key connecting factors for kinetochore and CENP-A assembly
inferredcites →https://doi.org/10.1242/jcs.243303openalex-snapshot
CENP-B creates alternative epigenetic chromatin states permissive for CENP-A or heterochromatin assembly
inferredcites →https://doi.org/10.1371/journal.pgen.1001342openalex-snapshot
A Molecular Phylogeny of Living Primates
inferredcites →https://doi.org/10.1371/journal.pgen.1004970openalex-snapshot
Naturally Occurring Differences in CENH3 Affect Chromosome Segregation in Zygotic Mitosis of Hybrids
inferredcites →https://doi.org/10.1371/journal.pgen.1009418openalex-snapshot
Selfish chromosomal drive shapes recent centromeric histone evolution in monkeyflowers
inferredcites →https://doi.org/10.3390/biology6010005openalex-snapshot
A Molecular View of Kinetochore Assembly and Function
inferredcites →https://doi.org/10.4161/cc.20633openalex-snapshot
Shugoshins function as a guardian for chromosomal stability in nuclear division
inferredcites →https://doi.org/10.4161/nucl.18955openalex-snapshot
CENP-C facilitates the recruitment of M18BP1 to centromeric chromatin
inferredcites →https://doi.org/10.7554/elife.21007openalex-snapshot
Molecular basis of outer kinetochore assembly on CENP-T
inferredcites →https://doi.org/10.7554/elife.33442openalex-snapshot
Decoding the centromeric nucleosome through CENP-N
inferredcites →https://doi.org/10.7554/elife.42989openalex-snapshot
Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
inferredcites →https://doi.org/10.7554/elife.49539openalex-snapshot
Molecular determinants of the Ska-Ndc80 interaction and their influence on microtubule tracking and force-coupling
inferredcites →https://doi.org/10.7554/elife.56582openalex-snapshot
Reconstitution reveals two paths of force transmission through the kinetochore

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1098/rsob.210074openalex-snapshot
Unravelling the mystery of female meiotic drive: where we are
inferred← citeshttps://doi.org/10.1186/s12864-021-07591-5openalex-snapshot
Population and subspecies diversity at mouse centromere satellites
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009494openalex-snapshot
Putting the brakes on centromere drive in Mimulus
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