نتایج جستجو برای: chromatid breakage

تعداد نتایج: 11316  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Chad Ellermeier Gerald R Smith

In preparation for the unique segregation of homologs at the first meiotic division, chromosomes undergo dramatic changes. The meiosis-specific sister chromatid cohesins Rec8 and Rec11 of Schizosaccharomyces pombe are recruited around the time of premeiotic replication, and Rec10, a component of meiosis-specific linear elements, is subsequently added. Here we report that Rec10 is essential for ...

Journal: :Cell 1991
C W Greider

Most people take the stability of chromosomes for granted. Some may imagine metaphase chromosomes lined up like a butterfly collection on a page, reassuringly in order and unchanging. However, evidence that has been accumulating for over half a century indicates that genome stability is a dynamic, not a static, process. In the 1940s natural chromosomes ends, or telomeres, were shown to be speci...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Alfredo Villasante José P Abad María Méndez-Lago

The centromere is the DNA region of the eukaryotic chromosome that determines kinetochore formation and sister chromatid cohesion. Centromeres interact with spindle microtubules to ensure the segregation of chromatids during mitosis and of homologous chromosomes in meiosis. The origin of centromeres, therefore, is inseparable from the evolution of cytoskeletal components that distribute chromos...

Journal: :The Journal of Cell Biology 2000
Cristina Machado Deborah J. Andrew

Previously, we reported that chromosomes contain a giant filamentous protein, which we identified as titin, a component of muscle sarcomeres. Here, we report the sequence of the entire titin gene in Drosophila melanogaster, D-Titin, and show that it encodes a two-megadalton protein with significant colinear homology to the NH(2)-terminal half of vertebrate titin. Mutations in D-Titin cause chro...

Journal: :Genetics 1964
J G BREWEN

T has been known for some time that there are differences in the radiationI induced chromosomal aberrations observed at metaphase, according to the stage of the cell cycle the cells were in at the time of irradiation (SWANSON 1957). The observed differences are not only quantitative (changes in frequency per cell), but are also qualitative in that, depending on the stage and the chromosomal stm...

2000
Cristina Machado Deborah J. Andrew

Previously, we reported that chromosomes contain a giant filamentous protein, which we identified as titin, a component of muscle sarcomeres. Here, we report the sequence of the entire titin gene in Drosophila melanogaster, D-Titin , and show that it encodes a two-megadalton protein with significant colinear homology to the NH 2 -terminal half of vertebrate titin. Mutations in D-Titin cause chr...

2015
Ryan G Thys Christine E Lehman Levi C. T Pierce Yuh-Hwa Wang

DNA has the ability to form a variety of secondary structures that can interfere with normal cellular processes, and many of these structures have been associated with neurological diseases and cancer. Secondary structure-forming sequences are often found at chromosomal fragile sites, which are hotspots for sister chromatid exchange, chromosomal translocations, and deletions. Structures formed ...

Journal: :Genetics 2002
Kara E Koehler Elise A Millie Jonathan P Cherry Paul S Burgoyne Edward P Evans Patricia A Hunt Terry J Hassold

The meiotic properties of paracentric inversion heterozygotes have been well studied in insects and plants, but not in mammalian species. In essence, a single meiotic recombination event within the inverted region results in the formation of a dicentric chromatid, which usually breaks or is stretched between the two daughter nuclei during the first meiotic anaphase. Here, we provide evidence th...

Journal: :Cancer genetics and cytogenetics 1983
A B Mitra V V Murty U K Luthra

Double-minute chromosomes (DMs) were observed in repeated samples in the leukocytes of a patient with a previous history of cervical carcinoma. The most interesting cytogenetic finding was the coexistence of DMs and a dicentric chromosome along with chromosome- and chromatid-type breaks and gaps. This observation suggests that DMs might originate through the breakage of existing chromosomes. Th...

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