ArticleNucleic acids research1992
Characterisation of a boundary between satellite III and alphoid sequences on human chromosome 10.
Article in Nucleic acids research, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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17 citing papers in PubMed, 35 citations in OpenAlex.
- DNMT3B PWWP mutations cause hypermethylation of heterochromatin.EMBO reports · 2024Article
- White spot syndrome viral protein VP9 alters the cellular higher-order chromatin structure.FASEB bioAdvances · 2020Article
- Genomic characterization of large heterochromatic gaps in the human genome assembly.PLoS computational biology · 2014Article
- Consensus higher order repeats and frequency of string distributions in human genome.Current genomics · 2007Article
- Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2001Article
- Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1999Article
- 1st International Conference on the Mammalian Centromere. Taichung, Taiwan, 2-4 October 1998. Abstracts.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1998Article
- Distribution and linkage of repetitive clusters from the heterochromatic region of human chromosome 22.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1996Article
- Transcripts from opposite strands of gamma satellite DNA are differentially expressed during mouse development.Mammalian genome : official journal of the International Mammalian Genome Society · 1995Article
- Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus.The EMBO journal · 1995Article
- New sites of methylcytosine-rich DNA detected on metaphase chromosomes.Human genetics · 1994Article
- Tandemly repeated pentanucleotides in DNA sequences of eucaryotes.Nucleic acids research · 1994Article
- Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes.Human genetics · 1994Article
- A multiple interval physical map of the pericentromeric region of human chromosome 10.Human genetics · 1994Article
- The organisation of repetitive sequences in the pericentromeric region of human chromosome 10.Nucleic acids research · 1993Article
- Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution.Nucleic acids research · 1993Article
- New nucleotide sequence data on the EMBL File Server.Nucleic acids research · 1992Article
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3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Alphoid and satellite III sequences are arranged as large tandem arrays in the centromeric regions of human chromosomes. Several recent studies using in situ hybridisation to investigate the relative positions of these sequences have shown that they occupy adjacent but non-overlapping domains in metaphase chromosomes. We have analysed the DNA sequence at the junction between alphoid and satellite III sequences in a cosmid previously mapped to chromosome 10. The alphoid sequence consists of tandemly arranged dimers which are distinct from the known chromosome 10-specific alphoid family. Polymerase chain reaction experiments confirm the integrity of the sequence data. These results, together with pulsed field gel electrophoresis data place the boundary between alphoid and satellite III sequences in the mapping interval 10 centromere-10q11.2. The sequence data shows that these repetitive sequences are separated by a partial L1 interspersed repeat sequence less than 500bp in length. The arrangement of the junction suggests that a recombination event has brought these sequences into close proximity.
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