Articles tagged with Kinetochores
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A research team at The University of Osaka has identified a parallel pathway involving CENP-C for centromere specification and function. This process is vital for ensuring chromosomes are structured and genes are expressed appropriately.
Researchers have discovered how key molecules coordinate chromosome alignment in cell division. Dual inhibition of KIF18A and CENP-E selectively kills cancer cells, suggesting a new therapeutic avenue for cancer treatment. This study highlights the importance of targeting specific proteins to develop more effective anticancer therapies.
The corona is a crucial structure in the kinetochore that ensures correct chromosome alignment and regulation of segregation. Scientists have discovered a dual-pathway assembly mechanism that drives corona formation from just two initial proteins.
The study reveals that centromeric R-loops play a critical role in ensuring chromosome alignment during oocyte meiotic divisions. Disruption of R-loop homeostasis leads to spindle assembly defects and chromosomal misalignment, highlighting the importance of R-loops in maintaining genomic stability.
Researchers at MPI unveiled PLK1's crucial role in replenishing CENP-A proteins per centromere, a process critical for cell division. PLK1 initiates a cascade of events by binding to specific machinery components and inducing phosphorylation changes.
A groundbreaking study has revealed that the centromere consists of two subdomains, which play a crucial role in ensuring proper chromosome segregation during cell division. This discovery provides new insights into the mechanisms underlying erroneous divisions in cancer cells.
The study reveals that CENP-E binds to protein complexes, forming a scaffold for the fibrous corona's development. This discovery sheds light on errors during cell division and could contribute to cancer treatment strategies.
A team at Osaka University identified a crucial protein facilitating proper chromosome movement when cells divide. The research revealed that the Cupin domain of CENP-C is essential for its function, supporting centromere/kinetochore assembly and maintaining genomic integrity.
Researchers at Osaka University used cryogenic electron microscopy to study the structural change of the centromere during cell division. The study revealed a complex interaction between proteins involved in cell division, providing new insights into the correct division of chromosomes.
The IPK research team has classified a key gene for cell division, highlighting its role in maintaining genome stability in plants. The study reveals that plant-specific duplicated genes have a significant impact on the centromere and kinetochore.
Researchers from Max Planck Institute have determined the 3D structural details of the human CCAN complex, highlighting its unique features and implications for interactions with centromere protein A. This discovery raises fundamental questions about creating artificial chromosomes.
Researchers have deciphered the structure of the kinetochore corona, a complex protein assembly that plays a pivotal role in chromosome segregation. The study, published in The EMBO Journal, provides new insights into how this critical process is regulated and offers a framework for future studies on cell division.
A complete, gapless genome sequence has been completed for scientists and physicians, revealing new details about the region around the centromere. The newly sequenced genome provides insights into human genetic variation and may hold clues to the evolution of our ancestors in Africa.
A team of researchers has discovered a unique organism that lacks essential genes for copying and distributing its DNA. The free-living protist Carpediemonas membranifera is unable to produce kinetochore proteins, which separate chromosomes during cell division.
Researchers at Max Planck Institute successfully rebuilt the kinetochore, a complex assembly of proteins that binds to microtubules, in vitro. The reconstruction is a significant milestone in understanding how the kinetochore functions and paves the way for creating synthetic chromosomes.
The study identifies Knl1 as a constitutive component of the central kinetochore protein in plants, playing an essential role in chromosomal congregation and segregation during mitosis. Deficiencies in Knl1 are linked to defective kernel development.
Researchers developed a novel probe to study how a 'matchmaker' molecule generates a 'wait' signal at kinetochores, ensuring accurate chromosome inheritance. This discovery provides insight into how accuracy of chromosome inheritance can be lowered in diseases like cancer.
Researchers from the Leibniz Institute of Plant Genetics and Crop Plant Research have discovered a chaperone protein that affects CenH3 loading to centromeres, crucial for kinetochore assembly. This finding has potential applications in plant breeding, particularly in haploid induction, which can speed up breeding processes.
A study published in Nature Cell Biology reveals the importance of the CENP-T pathway in ensuring accurate and timely chromosome segregation during cell division. The research, led by Osaka University, shows that this pathway is essential for successful mitosis and could lead to therapeutic options for diseases involving dysfunctional ...
Biologists at UMass Amherst have quantified the internal force during cell division, resolving a decades-long debate on how much force is involved. The study found that kinetochore fibers exert hundreds of piconewtons of poleward-directed force, settling the matter of how much force is brought to bear.
Researchers discovered a tension-sensitive molecule, Stu2, that ensures correct chromosome distribution during cell division. This 'fail safe' mechanism helps prevent aneuploidy, a genetic abnormality common in tumor cells.
Researchers have revealed the architecture of a protein complex called CCAN, which plays a foundational role in chromosome segregation during cell division. The study found that each subcomplex needs to touch many others to be functional, forming a mesh structure crucial for kinetochore assembly and stability.
Researchers have made a significant breakthrough in understanding the workings of an error correction mechanism that helps cells detect and correct mistakes in cell division. The study reveals the crucial importance of chromosome position in the spindle and how it affects division success, shedding light on aneuploidy prevention.
The American Association of Anatomists has awarded Young Investigators to R.R. Bensley Award winner Bungo Akiyoshi for his discovery of unconventional kinetochores in Kinetoplastids, and Feng Zhang for his contributions to comparative neuroanatomy through genome manipulations using CRISPR-Cas9.
Researchers found a strong, extra-tight linkage that joins sister chromatids in early stages of meiosis, preventing premature separation and misalignment. This discovery sheds light on the mechanisms that ensure proper distribution of chromosomes in healthy cells.
A team led by Yixian Zheng identified a protein that regulates interactions between kinetochores and microtubules, improving our understanding of chromosome alignment. The study suggests expanding the scope of research to include other cellular components for a deeper understanding of mitosis.
Researchers have identified a molecular surveillance system that helps detect and correct errors in cell division, preventing serious problems such as aneuploidy and cancer. The study reveals the importance of forces generated by molecular engines in regulating kinetochore-microtubule interactions.
Sue Biggins, a geneticist at Fred Hutchinson Cancer Center, received the National Academy of Sciences Award in Molecular Biology for her work on understanding cell division and isolating kinetochores. Her research sheds light on how kinetochores separate chromosomes during cell division, with potential implications for cancer treatment.
The kinetochore complex assembles preferentially at the ends of chromosomes, particularly in the telomeres, due to low chromatin turnover and absence of typical heterochromatin and euchromatin proteins. This suggests that epigenetic histone marks play a crucial role in determining kinetochore formation.
Researchers have discovered a mechanism for kinetochore formation that does not rely on the traditional centromere protein CENP-A. CENP-C and CENP-T/W complexes can direct functional kinetochore assembly, enabling accurate chromosome segregation. This breakthrough has implications for generating human artificial chromosomes.
Researchers discover CENP-C and CENP-T proteins, which are essential for kinetochore assembly and can potentially overcome the current obstacle of outfitting artificial chromosomes with kinetochores. This finding could lead to new genetic research tools and efficient creation of artificial human chromosomes.
Researchers have isolated and observed the kinetochore, a molecular complex that pulls chromosomes apart during cell division, outside of cells. The kinetochore's precise mechanism involves a balance of tension and disassembly to ensure accurate DNA replication.
Researchers found that a simple mechanism of finger-trap tension helps stabilize chromosomes during cell division, ensuring accurate gene distribution. This discovery could lead to new ways to correct defects before they occur or target cells with incorrect chromosome numbers to prevent further division.
Researchers have determined how cells regulate microtubule attachments during cell division, a process critical for proper chromosomal distribution. The system relies on phosphorylation and dephosphorylation of key proteins, controlled by enzymes Aurora B and PP1, to correct attachment problems and maintain accurate chromosome separation.
The Gerton Lab has determined the composition of centromeric chromatin in yeast cells, revealing an octameric structure composed of Cse4-containing nucleosomes. This discovery sheds light on mechanisms of centromere propagation and chromosome transmission, which are crucial for maintaining human health.
A team of University of Washington scientists has uncovered the basis for the strong yet dynamic attachment of spindle fibers to kinetochores, a site on each chromosome that mechanically couples to spindle fibers. This discovery sheds light on how chromosomes are accurately and evenly divided during cell division.