نتایج جستجو برای: centromeric index

تعداد نتایج: 398997  

Journal: :The Journal of Cell Biology 2002
Maki Murata-Hori Yu-li Wang

To address the mechanism that coordinates cytokinesis with mitosis, we have studied the dynamics of aurora B, a chromosomal passenger protein involved in signaling cytokinesis. Photobleaching analyses indicated dynamic exchange of aurora B between a centromeric and a cytoplasmic pool before anaphase onset, and stable associations with microtubules after anaphase onset. Bleaching near centromere...

Journal: :Trends in genetics : TIG 2014
Kristin C Scott Beth A Sullivan

Centromeres are essential for chromosome inheritance and genome stability. Centromeric proteins, including the centromeric histone centromere protein A (CENP-A), define the site of centromeric chromatin and kinetochore assembly. In many organisms, centromeres are located in or near regions of repetitive DNA. However, some atypical centromeres spontaneously form on unique sequences. These neocen...

2002
Helen Pomykala

A major unresolved question for the 11q23 translocations involving MLL is the chromosomal mechanism(s1 leading to these translocations. We have mapped breakpoints within the 8.3-kb BamHl breakpoint cluster region in 31 patients with acute lymphoblastic leukemia and acute myeloid leukemia (AML) de novo and in 8 t-AML patients. In 23 of 31 leukemia de novo patients, MLL breakpoints mapped to the ...

Journal: :Genetics 2013
Prashant K Mishra Alicia R Ottmann Munira A Basrai

The kinetochore (centromeric DNA and associated protein complex) is essential for faithful chromosome segregation and maintenance of genome stability. Here we report that an evolutionarily conserved protein Pat1 is a structural component of Saccharomyces cerevisiae kinetochore and associates with centromeres in a NDC10-dependent manner. Consistent with a role for Pat1 in kinetochore structure a...

Journal: :Genes & development 2005
Chryssa Kanellopoulou Stefan A Muljo Andrew L Kung Shridar Ganesan Ronny Drapkin Thomas Jenuwein David M Livingston Klaus Rajewsky

Dicer is the enzyme that cleaves double-stranded RNA (dsRNA) into 21-25-nt-long species responsible for sequence-specific RNA-induced gene silencing at the transcriptional, post-transcriptional, or translational level. We disrupted the dicer-1 (dcr-1) gene in mouse embryonic stem (ES) cells by conditional gene targeting and generated Dicer-null ES cells. These cells were viable, despite being c...

Journal: :The Plant cell 2002
Cathy Xiaoyan Zhong Joshua B Marshall Christopher Topp Rebecca Mroczek Akio Kato Kiyotaka Nagaki James A Birchler Jiming Jiang R Kelly Dawe

Maize centromeres are composed of CentC tandem repeat arrays, centromeric retrotransposons (CRs), and a variety of other repeats. One particularly well-conserved CR element, CRM, occurs primarily as complete and uninterrupted elements and is interspersed thoroughly with CentC at the light microscopic level. To determine if these major centromeric DNAs are part of the functional centromere/kinet...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Zhanyun Tang Yuxiao Sun Sara E Harley Hui Zou Hongtao Yu

Sister chromatids in mammalian cells remain attached mostly at their centromeres at metaphase because of the loss of cohesion along chromosome arms in prophase. Here, we report that Bub1 retains centromeric cohesion in mitosis of human cells. Depletion of Bub1 or Shugoshin (Sgo1) in HeLa cells by RNA interference causes massive missegregation of sister chromatids that originates at centromeres....

2011
Yuwen Ke Jae-Wan Huh Ross Warrington Bing Li Nan Wu Mei Leng Junmei Zhang Haydn L Ball Hongtao Yu

Centromeres nucleate the formation of kinetochores and are vital for chromosome segregation during mitosis. The SNF2 family helicase PICH (Plk1-interacting checkpoint helicase) and the BLM (the Bloom's syndrome protein) helicase decorate ultrafine histone-negative DNA threads that link the segregating sister centromeres during anaphase. The functions of PICH and BLM at these threads are not und...

Journal: :American journal of medical genetics 2002
Juliana Godoy Assumpção Windy Berkofsky-Fessler Nilma Viguetti Campos Andréa Trevas Maciel-Guerra Shulan Li Maria Isabel Melaragno Maricilda Palandi de Mello Peter E Warburton

An 18-year-old woman was evaluated because of primary amenorrhea and hypogonadism. Chromosome analysis from peripheral blood lymphocytes revealed a nonmosaic 46,X,+mar constitution. The marker was shown to be a rearranged Y chromosome consisting of an inverted duplication of the long arm: rea(Y)(qter-q11::q11-qter). Deletion mapping analysis with Y-specific STS showed that the marker lacked Yp ...

Journal: :Human molecular genetics 2001
R Weksberg J Nishikawa O Caluseriu Y L Fei C Shuman C Wei L Steele J Cameron A Smith I Ambus M Li P N Ray P Sadowski J Squire

Dysregulation of imprinted genes on human chromosome 11p15 has been implicated in Beckwith-Wiedemann syndrome (BWS), an overgrowth syndrome associated with congenital malformations and tumor predisposition. The molecular basis of BWS is complex and heterogeneous. The syndrome is associated with alterations in two distinct imprinting domains on 11p15: a telomeric domain containing the H19 and IG...

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