نتایج جستجو برای: subtelomeric translocation

تعداد نتایج: 47725  

Journal: :Journal of medical genetics 1998
S W Horsley S J Knight J Nixon S Huson M Fitchett R A Boone D Hilton-Jones J Flint L Kearney

We have previously described a fluorescence in situ hybridisation (FISH) assay for the simultaneous analysis of all human subtelomeric regions using a single microscope slide. Here we report the use of this multiprobe FISH assay in the study of a patient whose karyotype was reported by G banding analysis as 46,XX,del(18)(p11.2). Although the proband had some features suggestive of a chromosomal...

Journal: :The EMBO journal 2006
Anne-Sophie Berthiau Krassimir Yankulov Amadou Bah Emmanuelle Revardel Pierre Luciano Raymund J Wellinger Vincent Géli Eric Gilson

The Tbf1 and Reb1 proteins are present in yeast subtelomeric regions. We establish in this work that they inhibit telomerase-dependent lengthening of telomere. For example, tethering the N-terminal domain of Tbf1 and Reb1 in a subtelomeric region shortens that telomere proportionally to the number of domains bound. We further identified a 90 amino-acid long sequence within the N-terminal domain...

Journal: :The EMBO journal 1999
F E Pryde E J Louis

Silencing at native yeast telomeres, in which the subtelomeric elements are intact, is different from silencing at terminal truncations. The repression of URA3 inserted in different subtelomeric positions at several chromosome ends was investigated. Many ends exhibit very little silencing close to the telomere, while others exhibit substantial repression in limited domains. Silencing at native ...

Journal: :Human molecular genetics 2014
Shira Sagie Erika Ellran Hagar Katzir Rony Shaked Shiran Yehezkel Ilana Laevsky Alaa Ghanayim Dan Geiger Maty Tzukerman Sara Selig

Human telomeric regions are packaged as constitutive heterochromatin, characterized by extensive subtelomeric DNA methylation and specific histone modifications. ICF (immunodeficiency, centromeric instability, facial anomalies) type I patients carry mutations in DNA methyltransferase 3B (DNMT3B) that methylates de novo repetitive sequences during early embryonic development. ICF type I patient ...

2011
Jennifer J Smith Leslie R Miller Richard Kreisberg Laura Vazquez Yakun Wan John D Aitchison

Subtelomeric chromatin is subject to evolutionarily conserved complex epigenetic regulation and is implicated in numerous aspects of cellular function including formation of heterochromatin, regulation of stress response pathways and control of lifespan. Subtelomeric DNA is characterized by the presence of specific repeated segments that serve to propagate silencing or to protect chromosomal re...

2013
Cara A. Froyd Shivali Kapoor Fred Dietrich Laura N. Rusche

Deacetylases of the Sir2 or sirtuin family are thought to regulate life cycle progression and life span in response to nutrient availability. This family has undergone successive rounds of duplication and diversification, enabling the enzymes to perform a wide variety of biological functions. Two evolutionarily conserved functions of yeast Sir2 proteins are the generation of repressive chromati...

Journal: :Cytogenetic and genome research 2008
H Riethman

Copy number variation is a defining characteristic of human subtelomeres. Human subtelomeric segmental duplication regions ('Subtelomeric Repeats') comprise about 25% of the most distal 500 kb and 80% of the most distal 100 kb in human DNA. Huge allelic disparities seen in subtelomeric DNA sequence content and organization are postulated to have an impact on the dosage of transcripts embedded w...

2014
Lucy Glover David Horn

The African trypanosome, Trypanosoma brucei, is a parasitic protozoan that achieves antigenic variation through DNA-repair processes involving Variant Surface Glycoprotein (VSG) gene rearrangements at subtelomeres. Subtelomeric suppression of DNA repair operates in eukaryotes but little is known about these controls in trypanosomes. Here, we identify a trypanosome histone acetyltransferase (HAT...

2014
Shinjiro Kodama Tetsuya Yamada Junta Imai Shojiro Sawada Kei Takahashi Sohei Tsukita Keizo Kaneko Kenji Uno Yasushi Ishigaki Yoshitomo Oka Hideki Katagiri

Genetic factors play very important roles in the onset and progression of type 2 diabetes mellitus (T2DM). However, the genetic factors correlating with T2DM onset have not as yet been fully clarified. We previously found that copy number losses in the subtelomeric region on chromosome 4p16.3 were detected in early-onset Japanese T2DM patients (onset age <35 years) at a high frequency. Herein, ...

2015
Marta Kwapisz Myriam Ruault Erwin van Dijk Marc Descrimes Angela Taddei Antonin Morillon

Long non-coding RNAs (lncRNAs) have been shown to regulate gene expression, chromatin domains and chromosome stability in eukaryotic cells. Recent observations have reported the existence of telomeric repeats containing long ncRNAs – TERRA in mammalian and yeast cells. However, their functions remain poorly characterized. Here, we report the existence in S. cerevisiae of several lncRNAs within ...

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