scholarly journals Transcription of pericentromeric tandemly repeated DNA transcripts in human preovulatory oocytes

2019 ◽  
Vol 35 (3) ◽  
pp. 207-208
Author(s):  
M. A. Dobrynin ◽  
A. S. Kalugina ◽  
N. M. Korchagina ◽  
A. Prjibelski ◽  
O. I. Podgornaya ◽  
...  
Keyword(s):  
Repeated Dna ◽  
Tandemly Repeated Dna

Localization of tandemly repeated DNA sequences in Arabidopsis thaliana

1991 ◽  
Vol 1 (2) ◽  
pp. 159-166 ◽  
Author(s):  
J. Maluszynska ◽  
J.S. Heslop-Harrison
Keyword(s):  
Arabidopsis Thaliana ◽  
Dna Sequences ◽  
Repeated Dna ◽  
Repeated Dna Sequences ◽  
Tandemly Repeated Dna

A variable region of Anticarsia gemmatalis nuclear polyhedrosis virus contains tandemly repeated DNA sequences

1996 ◽  
Vol 41 (2) ◽  
pp. 123-132 ◽  
Author(s):  
Alejandra Garcia-Maruniak ◽  
Octavio H.O Pavan ◽  
James E Maruniak
Keyword(s):  
Dna Sequences ◽  
Nuclear Polyhedrosis Virus ◽  
Variable Region ◽  
Anticarsia Gemmatalis ◽  
Repeated Dna ◽  
Repeated Dna Sequences ◽  
Polyhedrosis Virus ◽  
Nuclear Polyhedrosis ◽  
Tandemly Repeated Dna

scholarly journals Chromosomal localization of a tandemly repeated DNA sequence in Trifolium repens L.

Cell Research ◽  
1996 ◽  
Vol 6 (1) ◽  
pp. 39-46 ◽  
Author(s):  
JM Zhu ◽  
NW Ellison ◽  
RW Rowland
Keyword(s):  
Dna Sequence ◽  
Trifolium Repens ◽  
Chromosomal Localization ◽  
Repeated Dna ◽  
Repeated Dna Sequence ◽  
Trifolium Repens L ◽  
Tandemly Repeated Dna Sequence ◽  
Tandemly Repeated Dna

Tandemly repeated DNA sequences from Xenopus laevis

1983 ◽  
Vol 165 (4) ◽  
pp. 567-585 ◽  
Author(s):  
Brenda S. Lam ◽  
Dana Carroll
Keyword(s):  
Xenopus Laevis ◽  
Dna Sequences ◽  
Repeated Dna ◽  
Repeated Dna Sequences ◽  
Tandemly Repeated Dna

Characterization of a major tandemly repeated DNA sequence (RBMII) prevalent among many species of waterfowl (Anatidae)

Genome ◽  
1992 ◽  
Vol 35 (6) ◽  
pp. 1037-1044 ◽  
Author(s):  
Cort S. Madsen ◽  
Kevin P. McHugh ◽  
Siwo R. de Kloet
Keyword(s):  
Dna Sequence ◽  
Sequence Variation ◽  
Sequence Divergence ◽  
Repeated Dna ◽  
Sequence Comparisons ◽  
Nonrandom Distribution ◽  
Repeated Dna Sequence ◽  
Tandemly Repeated Dna Sequence ◽  
Tandemly Repeated Dna

We have investigated the evolution of a 190 base pair tandemly repeated DNA sequence (RBMII) in 27 different species of waterfowl. In this paper we show that the RBMII sequence is present in many species belonging to 7 of the 11 Anatid tribes. Inter- and intra-tribal differences in repeat presence indicate that, although the RBMII sequence has been maintained among widely divergent species, it is rapidly evolving. Restriction enzyme analyses suggest very different hierarchical repeat organizations among different species. DNA sequence comparisons of 32 cloned monomer units from five different species revealed what appears to be a nonrandom distribution of sequence divergence, as well as large differences (up to 25-fold) in intraspecific sequence variation between relatively closely related species.Key words: repeated DNA, Anatidae, sequence variation.

The molecular structure, chromosomal organization, and interspecies distribution of a family of tandemly repeated DNA sequences of Antirrhinum majus L.

Genome ◽  
1996 ◽  
Vol 39 (2) ◽  
pp. 243-248 ◽  
Author(s):  
Thomas Schmidt ◽  
Jörg Kudla
Keyword(s):  
In Situ Hybridization ◽  
Dna Sequences ◽  
Satellite Dna ◽  
Antirrhinum Majus ◽  
Repeated Dna ◽  
Satellite Dnas ◽  
Repeated Dna Sequences ◽  
The North ◽  
Tandemly Repeated Dna

Monomers of a major family of tandemly repeated DNA sequences of Antirrhinum majus have been cloned and characterized. The repeats are 163–167 bp long, contain on average 60% A + T residues, and are organized in head-to-tail orientation. According to site-specific methylation differences two subsets of repeating units can be distinguished. Fluorescent in situ hybridization revealed that the repeats are localized at centromeric regions of six of the eight chromosome pairs of A. majus with substantial differences in array size. The monomeric unit shows no homologies to other plant satellite DNAs. The repeat exists in a similar copy number and conserved size in the genomes of six European species of the genus Antirrhinum. Tandemly repeated DNA sequences with homology to the cloned monomer were also found in the North American section Saerorhinum, indicating that this satellite DNA might be of ancient origin and was probably already present in the ancestral genome of both sections. Key words : Antirrhinum majus, satellite DNA, repetitive DNA, methylation, in situ hybridization.

Breakage of the human Y-chromosome short arm between two blocks of tandemly repeated DNA sequences

Genomics ◽  
1989 ◽  
Vol 5 (1) ◽  
pp. 153-156 ◽  
Author(s):  
Ulrich Müller ◽  
Marc Lalande ◽  
Timothy A. Donlon ◽  
Michael W. Heartlein
Keyword(s):  
Y Chromosome ◽  
Dna Sequences ◽  
Repeated Dna ◽  
Repeated Dna Sequences ◽  
Human Y Chromosome ◽  
Tandemly Repeated Dna

Instability of bacterial artificial chromosome (BAC) clones containing tandemly repeated DNA sequences

Genome ◽  
2001 ◽  
Vol 44 (3) ◽  
pp. 463-469 ◽  
Author(s):  
Junqi Song ◽  
Fenggao Dong ◽  
Jason W Lilly ◽  
Robert M Stupar ◽  
Jiming Jiang
Keyword(s):  
Dna Sequences ◽  
Tandem Repeats ◽  
Early Stage ◽  
Repeated Dna ◽  
Genome Research ◽  
Bac Clone ◽  
Artificial Chromosomes ◽  
Bac Clones ◽  
The Impact ◽  
Tandemly Repeated Dna

The cloning and propagation of large DNA fragments as bacterial artificial chromosomes (BACs) has become a valuable technique in genome research. BAC clones are highly stable in the host, Escherichia coli, a major advantage over yeast artificial chromosomes (YACs) in which recombination-induced instability is a major drawback. Here we report that BAC clones containing tandemly repeated DNA elements are not stable and can undergo drastic deletions during routine library maintenance and DNA preparation. Instability was observed in three BAC clones from sorghum, rice, and potato, each containing distinct tandem repeats. As many as 46% and 74% of the single colonies derived from a rice BAC clone containing 5S ribosomal RNA genes had insert deletions after 24 and 120 h of growth, respectively. We also demonstrated that BAC insert rearrangement can occur in the early stage of library construction and duplication. Thus, a minimum growth approach may not avoid the instability problem of such clones. The impact of BAC instability on genome research is discussed.Key words: repetitive DNA, large insert DNA library, genome research.

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