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Keywords: rDNA
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Journal Articles
J Cell Sci (2020) 133 (20): jcs242172.
Published: 30 October 2020
...-isometric nuclear envelope expansion resulting in an abnormal nuclear envelope shape. We further show that the tethering of rDNA to the nuclear envelope is required for the appearance of these extensions. * Author for correspondence ([email protected] ; [email protected] Handling Editor...
Includes: Supplementary data
Journal Articles
J Cell Sci (2005) 118 (24): 5777–5784.
Published: 15 December 2005
... to the DNA. We show that cells lacking Rqh1 are delayed in anaphase progression, and show lagging chromosomal DNA, which is particularly apparent in the rDNA locus. This mitotic delay is dependent on the spindle checkpoint, as deletion of mad2 abolishes the delay as well as the accumulation of Cut2 in rqh1 Δ...
Journal Articles
J Cell Sci (2000) 113 (18): 3207–3216.
Published: 15 September 2000
... of intrinsic, large-scale amplification mechanisms of mammalian cells. Here, we describe the successful generation of prototype human satellite DNA-based artificial chromosomes via amplification-dependent de novo chromosome formations induced by integration of exogenous DNA sequences into the centromeric/rDNA...
Journal Articles
J Cell Sci (1999) 112 (18): 3039–3047.
Published: 15 September 1999
... for correspondence (e-mail: [email protected]) 26 08 1999 09 07 1999 © 1999 by Company of Biologists 1999 Acrocentric chromosome RNA polymerase I Upstream binding factor (UBF) Zinc finger rDNA Many proteins have been found on mitotic chromosomes. Early examples were...
Journal Articles
J Cell Sci (1997) 110 (19): 2429–2440.
Published: 1 October 1997
...Jeannine Gébrane-Younès; Nathalie Fomproix; Danièle Hernandez-Verdun ABSTRACT The mechanisms that control inactivation of ribosomal gene (rDNA) transcription during mitosis is still an open question. To investigate this fundamental question, the precise timing of mitotic arrest was established...
Journal Articles
J Cell Sci (1994) 107 (3): 703–708.
Published: 1 March 1994
... has many DNA sequences in common with A chromosomes, showing no region rich in B-specific sequences. Six additional DNA probes were used to test the possible origin of this B from the standard NOR chromosome (chromosome 3). In the short arm of the NOR chromosome, we detected not only 18 S + 25 S rDNA...
Journal Articles
J Cell Sci (1993) 104 (4): 1199–1205.
Published: 1 April 1993
... chromosomes of stimulated lymphocytes. A novel procedure for isolating the intact fibrillar complex from LEP cells was used; the complex contains DNA that hybridizes to secondary constrictions of mitotic chromosomes and to 28 S rDNA sequences, on Southern blots. Electron microscopic DNA-DNA in situ...
Journal Articles
J Cell Sci (1993) 104 (3): 843–852.
Published: 1 March 1993
...Martin I. Highett; David J. Rawlins; Peter J. Shaw ABSTRACT We have used in situ hybridization with probes to rDNA, labelled either with digoxygenin or directly with fluorescein, to determine the arrangement of these genes within the nucleoli of Pisum sativum L. root cells. Confocal laser scanning...
Journal Articles
J Cell Sci (1992) 101 (4): 751–757.
Published: 1 April 1992
...A. R. Leitch; W. Mosg Öller; M. Shi; J. S. Heslop-Harrison ABSTRACT The physical location of the rDNA repeating units (25 S, 18 S and 5.8 S rRNA genes and the intergenic spacer sequences) was investigated in rye (Secale cereale L.) and wheat (Triticum aestivum L.) root tip meristematic cells...