On the public citation graph

Centromere-mediated chromosome break drives karyotype evolution in closely related Malassezia species

0 signed · 127 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/yea.2912openalex-snapshot

Optimization of ordered plasmid assembly by gap repair in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1007/978-3-642-00182-6_5openalex-snapshot

Evolutionary New Centromeres in Primates

inferredcites →https://doi.org/10.1007/s00239-005-0257-2openalex-snapshot

Evolution and Diversification of RNA Silencing Proteins in Fungi

inferredcites →https://doi.org/10.1007/s00294-016-0659-2openalex-snapshot

Isolation of conditional mutations in genes essential for viability of Cryptococcus neoformans

inferredcites →https://doi.org/10.1007/s00412-010-0278-5openalex-snapshot

Centromere inactivation and epigenetic modifications of a plant chromosome with three functional centromeres

inferredcites →https://doi.org/10.1007/s00412-012-0369-6openalex-snapshot

The evolutionary life cycle of the resilient centromere

inferredcites →https://doi.org/10.1016/0092-8674(82)90108-8openalex-snapshot

Nucleotide sequence comparisons and functional analysis of yeast centromere DNAs

inferredcites →https://doi.org/10.1016/0092-8674(89)90789-7openalex-snapshot

Composite motifs and repeat symmetry in S. pombe centromeres: Direct analysis by integration of Notl restriction sites

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.chom.2010.02.010openalex-snapshot

Functional Identification of the Plasmodium Centromere and Generation of a Plasmodium Artificial Chromosome

inferredcites →https://doi.org/10.1016/j.cub.2009.12.033openalex-snapshot

Mad2 Prolongs DNA Damage Checkpoint Arrest Caused by a Double-Strand Break via a Centromere-Dependent Mechanism

inferredcites →https://doi.org/10.1016/j.cub.2011.08.056openalex-snapshot

Endogenous Transcription at the Centromere Facilitates Centromere Activity in Budding Yeast

inferredcites →https://doi.org/10.1016/j.cub.2012.02.062openalex-snapshot

Epigenetic Inactivation and Subsequent Heterochromatinization of a Centromere Stabilize Dicentric Chromosomes

inferredcites →https://doi.org/10.1016/j.cub.2015.06.023openalex-snapshot

Discovery of an Unconventional Centromere in Budding Yeast Redefines Evolution of Point Centromeres

inferredcites →https://doi.org/10.1016/j.cub.2019.09.024openalex-snapshot

Early Diverging Fungus Mucor circinelloides Lacks Centromeric Histone CENP-A and Displays a Mosaic of Point and Regional Centromeres

inferredcites →https://doi.org/10.1016/j.mimet.2017.01.001openalex-snapshot

Highly efficient transformation system for Malassezia furfur and Malassezia pachydermatis using Agrobacterium tumefaciens-mediated transformation

inferredcites →https://doi.org/10.1016/j.molcel.2007.06.012openalex-snapshot

An AT-Rich Sequence in Human Common Fragile Site FRA16D Causes Fork Stalling and Chromosome Breakage in S. cerevisiae

inferredcites →https://doi.org/10.1016/j.molcel.2011.05.019openalex-snapshot

Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites

inferredcites →https://doi.org/10.1016/j.molcel.2011.10.013openalex-snapshot

Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes

inferredcites →https://doi.org/10.1016/j.tig.2005.09.009openalex-snapshot

Chromosome evolution in eukaryotes: a multi-kingdom perspective

inferredcites →https://doi.org/10.1016/j.tig.2011.03.004openalex-snapshot

Interpretation of karyotype evolution should consider chromosome structural constraints

inferredcites →https://doi.org/10.1016/j.tig.2018.05.001openalex-snapshot

Transcribing Centromeres: Noncoding RNAs and Kinetochore Assembly

inferredcites →https://doi.org/10.1016/s0723-2020(11)80043-3openalex-snapshot

Karyotyping of Malassezia Yeasts: Taxonomic and Epidemiological Implications

inferredcites →https://doi.org/10.1016/s1097-2765(03)00011-xopenalex-snapshot

A Cell Cycle-Regulated GATA Factor Promotes Centromeric Localization of CENP-A in Fission Yeast

inferredcites →https://doi.org/10.1038/287504a0openalex-snapshot

Isolation of a yeast centromere and construction of functional small circular chromosomes

inferredcites →https://doi.org/10.1038/nature01564openalex-snapshot

The methylated component of the Neurospora crassa genome

inferredcites →https://doi.org/10.1038/nature03154openalex-snapshot

Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

inferredcites →https://doi.org/10.1038/nature08842openalex-snapshot

Haploid plants produced by centromere-mediated genome elimination

inferredcites →https://doi.org/10.1038/nature08973openalex-snapshot

A three-dimensional model of the yeast genome

inferredcites →https://doi.org/10.1038/nature09745openalex-snapshot

Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site

inferredcites →https://doi.org/10.1038/nature10179openalex-snapshot

Condensin association with histone H2A shapes mitotic chromosomes

inferredcites →https://doi.org/10.1038/ng1289openalex-snapshot

Sequencing of a rice centromere uncovers active genes

inferredcites →https://doi.org/10.1038/nrc1714openalex-snapshot

On the road to cancer: aneuploidy and the mitotic checkpoint

inferredcites →https://doi.org/10.1038/s41586-019-1608-2openalex-snapshot

The fungal mycobiome promotes pancreatic oncogenesis via activation of MBL

inferredcites →https://doi.org/10.1038/sj.emboj.7600762openalex-snapshot

Molecular analysis of kinetochore architecture in fission yeast

inferredcites →https://doi.org/10.1073/pnas.0404318101openalex-snapshot

Centromeric DNA sequences in the pathogenic yeast Candida albicans are all different and unique

inferredcites →https://doi.org/10.1073/pnas.0809770105openalex-snapshot

Rapid evolution of Cse4p-rich centromeric DNA sequences in closely related pathogenic yeasts, Candida albicans and Candida dubliniensis

inferredcites →https://doi.org/10.1073/pnas.0912143106openalex-snapshot

Centromere-localized breaks indicate the generation of DNA damage by the mitotic spindle

inferredcites →https://doi.org/10.1073/pnas.1103190108openalex-snapshot

Loss of centromeric histone H3 (CENH3) from centromeres precedes uniparental chromosome elimination in interspecific barley hybrids

inferredcites →https://doi.org/10.1073/pnas.1508749112openalex-snapshot

Regional centromeres in the yeast Candida lusitaniae lack pericentromeric heterochromatin

inferredcites →https://doi.org/10.1073/pnas.1700764114openalex-snapshot

Diatom centromeres suggest a mechanism for nuclear DNA acquisition

inferredcites →https://doi.org/10.1073/pnas.1713725115openalex-snapshot

RNAi is a critical determinant of centromere evolution in closely related fungi

inferredcites →https://doi.org/10.1073/pnas.1821384116openalex-snapshot

Point centromere activity requires an optimal level of centromeric noncoding RNA

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

Mosaic origin of the eukaryotic kinetochore

inferredcites →https://doi.org/10.1073/pnas.88.20.9051openalex-snapshot

Origin of human chromosome 2: an ancestral telomere-telomere fusion.

inferredcites →https://doi.org/10.1073/pnas.97.23.12583openalex-snapshot

Interaction of yeast kinetochore proteins with centromere–protein/transcription factor Cbf1

inferredcites →https://doi.org/10.1074/jbc.m200265200openalex-snapshot

Efficient Rejoining of Radiation-induced DNA Double-strand Breaks in Centromeric DNA of Human Cells

inferredcites →https://doi.org/10.1080/02681219880000581openalex-snapshot

Molecular typing ofMalasseziaspecies with PFGE and RAPD

inferredcites →https://doi.org/10.1083/jcb.153.3.517openalex-snapshot

Merotelic Kinetochore Orientation Is a Major Mechanism of Aneuploidy in Mitotic Mammalian Tissue Cells

inferredcites →https://doi.org/10.1083/jcb.200210005openalex-snapshot

Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway

inferredcites →https://doi.org/10.1083/jcb.200305100openalex-snapshot

Architecture of the budding yeast kinetochore reveals a conserved molecular core

inferredcites →https://doi.org/10.1083/jcb.201611087openalex-snapshot

Centromere transcription allows CENP-A to transit from chromatin association to stable incorporation

inferredcites →https://doi.org/10.1091/mbc.3.7.819openalex-snapshot

A low copy number central sequence with strict symmetry and unusual chromatin structure in fission yeast centromere.

inferredcites →https://doi.org/10.1091/mbc.5.7.747openalex-snapshot

The centromeric K-type repeat and the central core are together sufficient to establish a functional Schizosaccharomyces pombe centromere.

inferredcites →https://doi.org/10.1091/mbc.e13-05-0229openalex-snapshot

Monopolin recruits condensin to organize centromere DNA and repetitive DNA sequences

inferredcites →https://doi.org/10.1093/bioinformatics/btq102openalex-snapshot

Genome-wide synteny through highly sensitive sequence alignment: Satsuma

inferredcites →https://doi.org/10.1093/bioinformatics/btr039openalex-snapshot

Easyfig: a genome comparison visualizer

inferredcites →https://doi.org/10.1093/carcin/bgr069openalex-snapshot

Centromere fission, not telomere erosion, triggers chromosomal instability in human carcinomas

inferredcites →https://doi.org/10.1093/emboj/20.8.2087openalex-snapshot

A 330 kb CENP‐A binding domain and altered replication timing at a human neocentromere

inferredcites →https://doi.org/10.1093/gbe/evq042openalex-snapshot

Chromosomal G + C Content Evolution in Yeasts: Systematic Interspecies Differences, and GC-Poor Troughs at Centromeres

inferredcites →https://doi.org/10.1093/gbe/evw178openalex-snapshot

Centromeres of the Yeast Komagataella phaffii ( Pichia pastoris) Have a Simple Inverted-Repeat Structure

inferredcites →https://doi.org/10.1093/genetics/26.2.234openalex-snapshot

THE STABILITY OF BROKEN ENDS OF CHROMOSOMES IN ZEA MAYS

inferredcites →https://doi.org/10.1093/mmy/myx134openalex-snapshot

Malassezia ecology, pathophysiology, and treatment

inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot

IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies

inferredcites →https://doi.org/10.1093/nar/gkr123openalex-snapshot

SyMAP v3.4: a turnkey synteny system with application to plant genomes

inferredcites →https://doi.org/10.1093/nar/gks921openalex-snapshot

Transcription in the maintenance of centromere chromatin identity

inferredcites →https://doi.org/10.1093/nar/gkx006openalex-snapshot

Proteogenomics produces comprehensive and highly accurate protein-coding gene annotation in a complete genome assembly ofMalassezia sympodialis

inferredcites →https://doi.org/10.1093/nar/gkz239openalex-snapshot

Interactive Tree Of Life (iTOL) v4: recent updates and new developments

inferredcites →https://doi.org/10.1101/gad.13.13.1664openalex-snapshot

Proper metaphase spindle length is determined by centromere proteins Mis12 and Mis6 required for faithful chromosome segregation

inferredcites →https://doi.org/10.1101/gad.340905openalex-snapshot

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability

inferredcites →https://doi.org/10.1101/gr.092759.109openalex-snapshot

Circos: An information aesthetic for comparative genomics

inferredcites →https://doi.org/10.1101/gr.109744.110openalex-snapshot

Ancestral grass karyotype reconstruction unravels new mechanisms of genome shuffling as a source of plant evolution

inferredcites →https://doi.org/10.1101/gr.116202.110openalex-snapshot

Distinct DNA methylation patterns associated with active and inactive centromeres of the maize B chromosome

inferredcites →https://doi.org/10.1101/gr.160887.113openalex-snapshot

Maize centromeres expand and adopt a uniform size in the genetic background of oat

inferredcites →https://doi.org/10.1101/gr.3672305openalex-snapshot

The Yeast Gene Order Browser: Combining curated homology and syntenic context reveals gene fate in polyploid species

inferredcites →https://doi.org/10.1105/tpc.109.066662openalex-snapshot

Reactivation of an Inactive Centromere Reveals Epigenetic and Structural Components for Centromere Specification in Maize

inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00394.xopenalex-snapshot

DIVERSIFICATION IN SEXUAL AND ASEXUAL ORGANISMS

inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07558.xopenalex-snapshot

CaMtw1, a member of the evolutionarily conserved Mis12 kinetochore protein family, is required for efficient inner kinetochore assembly in the pathogenic yeast Candida albicans

inferredcites →https://doi.org/10.1111/nph.12885openalex-snapshot

Live and let die: centromere loss during evolution of plant chromosomes

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.1074973openalex-snapshot

Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi

inferredcites →https://doi.org/10.1126/science.1158699openalex-snapshot

Heterochromatin Integrity Affects Chromosome Reorganization After Centromere Dysfunction

inferredcites →https://doi.org/10.1126/science.1203357openalex-snapshot

Comparative Functional Genomics of the Fission Yeasts

inferredcites →https://doi.org/10.1126/science.7063861openalex-snapshot

The Origin of Man: A Chromosomal Pictorial Legacy

inferredcites →https://doi.org/10.1128/aem.02411-13openalex-snapshot

GET_HOMOLOGUES, a Versatile Software Package for Scalable and Robust Microbial Pangenome Analysis

inferredcites →https://doi.org/10.1128/ec.05165-11openalex-snapshot

Diversity in Requirement of Genetic and Epigenetic Factors for Centromere Function in Fungi

inferredcites →https://doi.org/10.1128/ec.1.2.229-240.2002openalex-snapshot

Nnf1p, Dsn1p, Mtw1p, and Nsl1p: a New Group of Proteins Important for Chromosome Segregation in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1128/jcm.41.10.4695-4699.2003openalex-snapshot

Description of a New Yeast Species, Malassezia japonica , and Its Detection in Patients with Atopic Dermatitis and Healthy Subjects

inferredcites →https://doi.org/10.1128/mbio.01581-19openalex-snapshot

Cellular Dynamics and Genomic Identity of Centromeres in Cereal Blast Fungus

inferredcites →https://doi.org/10.1128/mbio.01752-17openalex-snapshot

FKBP12-Dependent Inhibition of Calcineurin Mediates Immunosuppressive Antifungal Drug Action in Malassezia

inferredcites →https://doi.org/10.1128/mbio.01853-16openalex-snapshot

Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen Malassezia Genus

inferredcites →https://doi.org/10.1128/mbio.02055-17openalex-snapshot

Erratum for Ianiri et al., “FKBP12-Dependent Inhibition of Calcineurin Mediates Immunosuppressive Antifungal Drug Action in Malassezia ”

inferredcites →https://doi.org/10.1128/mcb.10.5.1863openalex-snapshot

Functional Analysis of a Centromere from Fission Yeast: A Role for Centromere-Specific Repeated DNA Sequences

inferredcites →https://doi.org/10.1128/mcb.12.9.4056openalex-snapshot

Replication Forks Pause at Yeast Centromeres

inferredcites →https://doi.org/10.1128/mcb.15.9.5165openalex-snapshot

Replication of Centromere II of Schizosaccharomyces pombe

inferredcites →https://doi.org/10.1186/1747-1028-5-13openalex-snapshot

Merotelic attachments and non-homologous end joining are the basis of chromosomal instability

inferredcites →https://doi.org/10.1186/1747-1028-5-15openalex-snapshot

One-hit wonders of genomic instability

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/jbiol11openalex-snapshot

Adaptive evolution of centromere proteins in plants and animals

inferredcites →https://doi.org/10.1186/s13072-015-0033-5openalex-snapshot

Histone modifications rather than the novel regional centromeres of Zymoseptoria tritici distinguish core and accessory chromosomes

inferredcites →https://doi.org/10.1242/jcs.00716openalex-snapshot

Merotelic kinetochore orientation occurs frequently during early mitosis in mammalian tissue cells and error correction is achieved by two different mechanisms

inferredcites →https://doi.org/10.1371/journal.pbio.2002527openalex-snapshot

Fungal genome and mating system transitions facilitated by chromosomal translocations involving intercentromeric recombination

inferredcites →https://doi.org/10.1371/journal.pcbi.0010067openalex-snapshot

PhyloGibbs: A Gibbs Sampling Motif Finder That Incorporates Phylogeny

inferredcites →https://doi.org/10.1371/journal.pcbi.1000156openalex-snapshot

PhyloGibbs-MP: Module Prediction and Discriminative Motif-Finding by Gibbs Sampling

inferredcites →https://doi.org/10.1371/journal.pcbi.1000392openalex-snapshot

Fast Statistical Alignment

inferredcites →https://doi.org/10.1371/journal.pgen.1000835openalex-snapshot

DNA Binding of Centromere Protein C (CENPC) Is Stabilized by Single-Stranded RNA

inferredcites →https://doi.org/10.1371/journal.pgen.1001061openalex-snapshot

Telomere Disruption Results in Non-Random Formation of De Novo Dicentric Chromosomes Involving Acrocentric Human Chromosomes

inferredcites →https://doi.org/10.1371/journal.pgen.1002190openalex-snapshot

Mechanisms of Chromosome Number Evolution in Yeast

inferredcites →https://doi.org/10.1371/journal.pgen.1002528openalex-snapshot

Discovery of a Modified Tetrapolar Sexual Cycle in Cryptococcus amylolentus and the Evolution of MAT in the Cryptococcus Species Complex

inferredcites →https://doi.org/10.1371/journal.pgen.1004344openalex-snapshot

Rad51–Rad52 Mediated Maintenance of Centromeric Chromatin in Candida albicans

inferredcites →https://doi.org/10.1371/journal.pgen.1004849openalex-snapshot

Unisexual Reproduction Drives Meiotic Recombination and Phenotypic and Karyotypic Plasticity in Cryptococcus neoformans

inferredcites →https://doi.org/10.1371/journal.pgen.1005614openalex-snapshot

Genus-Wide Comparative Genomics of Malassezia Delineates Its Phylogeny, Physiology, and Niche Adaptation on Human Skin

inferredcites →https://doi.org/10.1371/journal.pgen.1005839openalex-snapshot

Repeat-Associated Fission Yeast-Like Regional Centromeres in the Ascomycetous Budding Yeast Candida tropicalis

inferredcites →https://doi.org/10.1371/journal.ppat.1002701openalex-snapshot

Malassezia Fungi Are Specialized to Live on Skin and Associated with Dandruff, Eczema, and Other Skin Diseases

inferredcites →https://doi.org/10.1371/journal.ppat.1004277openalex-snapshot

From Dandruff to Deep-Sea Vents: Malassezia-like Fungi Are Ecologically Hyper-diverse

inferredcites →https://doi.org/10.1371/journal.ppat.1004436openalex-snapshot

The Skin Microbiome: A Focus on Pathogens and Their Association with Skin Disease

inferredcites →https://doi.org/10.1371/journal.ppat.1007150openalex-snapshot

Five pillars of centromeric chromatin in fungal pathogens

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/10.1534/genetics.107.083980openalex-snapshot

Rapid Evolution of Yeast Centromeres in the Absence of Drive

inferredcites →https://doi.org/10.3389/fmicb.2016.00759openalex-snapshot

The Chromatin of Candida albicans Pericentromeres Bears Features of Both Euchromatin and Heterochromatin

inferredcites →https://doi.org/10.3390/biology6010005openalex-snapshot

A Molecular View of Kinetochore Assembly and Function

inferredcites →https://doi.org/10.3767/persoonia.2018.41.04openalex-snapshot

Malassezia vespertilionis sp. nov.: a new cold-tolerant species of yeast isolated from bats

inferredcites →https://doi.org/10.4014/jmb.1810.10019openalex-snapshot

Genomic Tandem Quadruplication is Associated with Ketoconazole Resistance in Malassezia pachydermatis

inferredcites →https://doi.org/10.4161/cc.9.17.12885openalex-snapshot

The Lrs4-Csm1 monopolin complex associates with kinetochores during anaphase and is required for accurate chromosome segregation

inferredcites →https://doi.org/10.4161/cc.9.19.13233openalex-snapshot

Laser microsurgery provides evidence for merotelic kinetochore attachments in fission yeast cells lacking Pcs1 or Clr4

inferredcites →https://doi.org/10.7554/elife.56026openalex-snapshot

Centromere deletion in Cryptococcus deuterogattii leads to neocentromere formation and chromosome fusions

What points at this work

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

inferred← citeshttps://doi.org/10.1146/annurev-genet-120116-024755openalex-snapshot

The Evolution of Sexual Reproduction and the Mating-Type Locus: Links to Pathogenesis of Cryptococcus Human Pathogenic Fungi

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.