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Molecular evolution of the mammalian kinetochore complex

https://doi.org/10.1101/2024.06.27.600994

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb08066.xopenalex-snapshot

CENP‐E, a novel human centromere‐associated protein required for progression from metaphase to anaphase.

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/10.1007/978-1-62703-646-7_10openalex-snapshot

Phylogeny-aware alignment with PRANK

inferredcites →https://doi.org/10.1007/978-3-642-00182-6_2openalex-snapshot

The Centromere-Drive Hypothesis: A Simple Basis for Centromere Complexity

inferredcites →https://doi.org/10.1007/bf00160320openalex-snapshot

Presence and abundance of CENP-B box sequences in great ape subsets of primate-specific ?-satellite DNA

inferredcites →https://doi.org/10.1007/s00412-016-0608-3openalex-snapshot

Kinetochore assembly and function through the cell cycle

inferredcites →https://doi.org/10.1007/s10577-014-9404-1openalex-snapshot

The CENP-O complex requirement varies among different cell types

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.2013.01.035openalex-snapshot

Identifying Recent Adaptations in Large-Scale Genomic Data

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.cell.2021.07.037openalex-snapshot

Parallel pathways for recruiting effector proteins determine centromere drive and suppression

inferredcites →https://doi.org/10.1016/j.celrep.2021.109740openalex-snapshot

Bub1 and CENP-U redundantly recruit Plk1 to stabilize kinetochore-microtubule attachments and ensure accurate chromosome segregation

inferredcites →https://doi.org/10.1016/j.cub.2010.12.039openalex-snapshot

Direct Binding of Cenp-C to the Mis12 Complex Joins the Inner and Outer Kinetochore

inferredcites →https://doi.org/10.1016/j.cub.2011.02.005openalex-snapshot

CENP-C Is a Structural Platform for Kinetochore Assembly

inferredcites →https://doi.org/10.1016/j.cub.2011.09.044openalex-snapshot

Synaptonemal Complex-Dependent Centromeric Clustering and the Initiation of Synapsis in Drosophila Oocytes

inferredcites →https://doi.org/10.1016/j.cub.2013.06.040openalex-snapshot

Lateral to End-on Conversion of Chromosome-Microtubule Attachment Requires Kinesins CENP-E and MCAK

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.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.devcel.2006.04.017openalex-snapshot

Sister Chromatid Cohesion at the Centromere: Confrontation between Kinases and Phosphatases?

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.ebiom.2016.02.043openalex-snapshot

A Selective Small Molecule DNA2 Inhibitor for Sensitization of Human Cancer Cells to Chemotherapy

inferredcites →https://doi.org/10.1016/j.molcel.2016.06.023openalex-snapshot

The Flexible Ends of CENP-A Nucleosome Are Required for Mitotic Fidelity

inferredcites →https://doi.org/10.1016/j.tcb.2016.01.005openalex-snapshot

Evolutionary Turnover of Kinetochore Proteins: A Ship of Theseus?

inferredcites →https://doi.org/10.1016/s0092-8674(00)80419-5openalex-snapshot

CENP-E Is a Plus End–Directed Kinetochore Motor Required for Metaphase Chromosome Alignment

inferredcites →https://doi.org/10.1016/s1534-5807(02)00255-1openalex-snapshot

Unstable Kinetochore-Microtubule Capture and Chromosomal Instability Following Deletion of CENP-E

inferredcites →https://doi.org/10.1038/35019518openalex-snapshot

CENP-E forms a link between attachment of spindle microtubules to kinetochores and the mitotic checkpoint

inferredcites →https://doi.org/10.1038/371215a0openalex-snapshot

The evolutionary dynamics of repetitive DNA in eukaryotes

inferredcites →https://doi.org/10.1038/nature06250openalex-snapshot

Genome-wide detection and characterization of positive selection in human populations

inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot

A global reference for human genetic variation

inferredcites →https://doi.org/10.1038/ncb1397openalex-snapshot

The human CENP-A centromeric nucleosome-associated complex

inferredcites →https://doi.org/10.1038/ncb2831openalex-snapshot

Kinetochore kinesin CENP-E is a processive bi-directional tracker of dynamic microtubule tips

inferredcites →https://doi.org/10.1038/nrm.2015.5openalex-snapshot

The molecular basis for centromere identity and function

inferredcites →https://doi.org/10.1038/nrm2310openalex-snapshot

Molecular architecture of the kinetochore–microtubule interface

inferredcites →https://doi.org/10.1038/nsb996openalex-snapshot

Phylogenomics of the nucleosome

inferredcites →https://doi.org/10.1038/nsmb.3175openalex-snapshot

CENP-C directs a structural transition of CENP-A nucleosomes mainly through sliding of DNA gyres

inferredcites →https://doi.org/10.1038/s41586-024-07278-3openalex-snapshot

The variation and evolution of complete human centromeres

inferredcites →https://doi.org/10.1038/sdata.2016.75openalex-snapshot

Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus

inferredcites →https://doi.org/10.1038/srep17197openalex-snapshot

Widespread Positive Selection Drives Differentiation of Centromeric Proteins in the Drosophila melanogaster subgroup

inferredcites →https://doi.org/10.1073/pnas.032664299openalex-snapshot

Recurrent evolution of DNA-binding motifs in the Drosophila centromeric histone

inferredcites →https://doi.org/10.1073/pnas.0408600102openalex-snapshot

Human Bub1 protects centromeric sister-chromatid cohesion through Shugoshin during mitosis

inferredcites →https://doi.org/10.1073/pnas.1317042110openalex-snapshot

Chromosome missegregation rate predicts whether aneuploidy will promote or suppress tumors

inferredcites →https://doi.org/10.1073/pnas.1821945116openalex-snapshot

Mosaic origin of the eukaryotic kinetochore

inferredcites →https://doi.org/10.1074/jbc.m110.189340openalex-snapshot

Biophysical Characterization of the Centromere-specific Nucleosome from Budding Yeast

inferredcites →https://doi.org/10.1074/jbc.m306477200openalex-snapshot

CENP-B Interacts with CENP-C Domains Containing Mif2 Regions Responsible for Centromere Localization

inferredcites →https://doi.org/10.1074/jbc.ra118.003154openalex-snapshot

The kinetochore proteins CENP-E and CENP-F directly and specifically interact with distinct BUB mitotic checkpoint Ser/Thr kinases

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.130.3.507openalex-snapshot

CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis.

inferredcites →https://doi.org/10.1083/jcb.139.6.1373openalex-snapshot

CENP-E Function at Kinetochores Is Essential for Chromosome Alignment

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.200802189openalex-snapshot

CENP-E combines a slow, processive motor and a flexible coiled coil to produce an essential motile kinetochore tether

inferredcites →https://doi.org/10.1083/jcb.201001013openalex-snapshot

Dual recognition of CENP-A nucleosomes is required for centromere assembly

inferredcites →https://doi.org/10.1083/jcb.201905018openalex-snapshot

CENP-F stabilizes kinetochore-microtubule attachments and limits dynein stripping of corona cargoes

inferredcites →https://doi.org/10.1091/mbc.e07-06-0556openalex-snapshot

CENP-O Class Proteins Form a Stable Complex and Are Required for Proper Kinetochore Function

inferredcites →https://doi.org/10.1093/bioinformatics/13.5.555openalex-snapshot

PAML: a program package for phylogenetic analysis by maximum likelihood

inferredcites →https://doi.org/10.1093/emboj/cdf612openalex-snapshot

Variation in satellite DNA profiles—causes and effects

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/molbev/msad041openalex-snapshot

Beginner's Guide on the Use of PAML to Detect Positive Selection

inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot

PAML 4: Phylogenetic Analysis by Maximum Likelihood

inferredcites →https://doi.org/10.1093/molbev/msq043openalex-snapshot

Adaptive Evolution of Foundation Kinetochore Proteins in Primates

inferredcites →https://doi.org/10.1093/molbev/msr177openalex-snapshot

Improving the Performance of Positive Selection Inference by Filtering Unreliable Alignment Regions

inferredcites →https://doi.org/10.1093/molbev/msz140openalex-snapshot

Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects

inferredcites →https://doi.org/10.1093/nar/16.24.11645openalex-snapshot

Sequence organization and cytological localization of the minor satellite of mouse

inferredcites →https://doi.org/10.1093/nar/gkq443openalex-snapshot

GUIDANCE: a web server for assessing alignment confidence scores

inferredcites →https://doi.org/10.1093/nar/gkt1124openalex-snapshot

The centromeric nucleosome-like CENP–T–W–S–X complex induces positive supercoils into DNA

inferredcites →https://doi.org/10.1093/nar/gkv405openalex-snapshot

Stable complex formation of CENP-B with the CENP-A nucleosome

inferredcites →https://doi.org/10.1098/rsbl.2015.0817openalex-snapshot

CENP-B box, a nucleotide motif involved in centromere formation, occurs in a New World monkey

inferredcites →https://doi.org/10.1098/rstb.2004.1607openalex-snapshot

Shugoshin protects cohesin complexes at centromeres - Discussion

inferredcites →https://doi.org/10.1101/gad.1227304openalex-snapshot

A role for centromere pairing in meiotic chromosome segregation

inferredcites →https://doi.org/10.1101/gad.1709408openalex-snapshot

Initiation of meiotic chromosome synapsis at centromeres in budding yeast

inferredcites →https://doi.org/10.1101/gad.329705openalex-snapshot

Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation

inferredcites →https://doi.org/10.1101/gr.111278.110openalex-snapshot

Genome-wide characterization of centromeric satellites from multiple mammalian genomes

inferredcites →https://doi.org/10.1101/gr.132647.111openalex-snapshot

Evolutionary rate covariation reveals shared functionality and coexpression of genes

inferredcites →https://doi.org/10.1101/sqb.1991.056.01.076openalex-snapshot

Role of the Centromere/Kinetochore in Cell Cycle Control

inferredcites →https://doi.org/10.1111/evo.13850openalex-snapshot

Molecular evolution of the meiotic recombination pathway in mammals

inferredcites →https://doi.org/10.1111/mec.15812openalex-snapshot

Kinetochore proteins and microtubule‐destabilizing factors are fast evolving in eutherian mammals

inferredcites →https://doi.org/10.1126/sciadv.adi5764openalex-snapshot

Centromere innovations within a mouse species

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.1235532openalex-snapshot

A Conserved Mechanism for Centromeric Nucleosome Recognition by Centromere Protein CENP-C

inferredcites →https://doi.org/10.1126/science.1259308openalex-snapshot

CENP-C reshapes and stabilizes CENP-A nucleosomes at the centromere

inferredcites →https://doi.org/10.1128/mcb.15.8.4009openalex-snapshot

CENP-B Binds a Novel Centromeric Sequence in the Asian Mouse Mus caroli

inferredcites →https://doi.org/10.1128/mcb.16.9.5156openalex-snapshot

Surprising Deficiency of CENP-B Binding Sites in African Green Monkey α-Satellite DNA: Implications for CENP-B Function at Centromeres

inferredcites →https://doi.org/10.1128/mcb.25.10.4062-4074.2005openalex-snapshot

Silencing Mitosin Induces Misaligned Chromosomes, Premature Chromosome Decondensation before Anaphase Onset, and Mitotic Cell Death

inferredcites →https://doi.org/10.1186/gb-2006-7-3-r23openalex-snapshot

Phylogenetic and structural analysis of centromeric DNA and kinetochore proteins

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/s12915-021-01165-3openalex-snapshot

Selection shapes the landscape of functional variation in wild house mice

inferredcites →https://doi.org/10.1242/jcs.01006openalex-snapshot

Bub1 is required for kinetochore localization of BubR1, Cenp-E, Cenp-F and Mad2, and chromosome congression

inferredcites →https://doi.org/10.1266/ggs.86.357openalex-snapshot

Structure of the CENP-A nucleosome and its implications for centromeric chromatin architecture

inferredcites →https://doi.org/10.1371/journal.pgen.1002790openalex-snapshot

Interplay between Synaptonemal Complex, Homologous Recombination, and Centromeres during Mammalian Meiosis

inferredcites →https://doi.org/10.1371/journal.pgen.1007672openalex-snapshot

The genomic basis of environmental adaptation in house mice

inferredcites →https://doi.org/10.1371/journal.pone.0005832openalex-snapshot

The C-Terminal Domain of CENP-C Displays Multiple and Critical Functions for Mammalian Centromere Formation

inferredcites →https://doi.org/10.15252/embr.201744102openalex-snapshot

Evolutionary dynamics of the kinetochore network in eukaryotes as revealed by comparative genomics

inferredcites →https://doi.org/10.3390/genes9120615openalex-snapshot

Repetitive Fragile Sites: Centromere Satellite DNA as a Source of Genome Instability in Human Diseases

inferredcites →https://doi.org/10.4137/ebo.s19199openalex-snapshot

Evaluating the Accuracy and Efficiency of Multiple Sequence Alignment Methods

What points at this work

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

inferred← citeshttps://doi.org/10.1038/s41586-025-09779-1openalex-snapshot

Progressive coevolution of the yeast centromere and kinetochore

inferred← citeshttps://doi.org/10.64898/2026.02.13.705784openalex-snapshot

Assessing positive selection in centromere-associated kinetochore proteins across Metazoan groups

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