Literature DB >> 3032768

Chromosomal location by in situ hybridization of the human Sau3A family of DNA repeats.

A Agresti, G Rainaldi, A Lobbiani, I Magnani, R Di Lernia, R Meneveri, A G Siccardi, E Ginelli.   

Abstract

The Sau3A family is a human, clustered, highly repetitive, GC-rich DNA family. In situ hybridization studies with a plasmid carrying a Sau3A monomer as a probe have shown that Sau3A sequences are preferentially concentrated in the heterochromatic regions of human acrocentric chromosomes (D and G groups, both in pericentromeric regions and in cytological satellites) and in pericentromeric heterochromatin of chromosome 1. The same chromosomal locations were observed by using as probes two recombinant phages which carry Sau3A-positive genomic sectors. The two sectors differ for the relative proportions of monomer and multiples of Sau3A repeats, which show different extents of homology to the cloned monomer, and for the presence, in one of the two, of a small amount of an unrelated repeat (alphoid DNA). The similarity of the results obtained with the three probes suggests that heterogeneous Sau3A repeats share the same chromosomal localizations and that the two analyzed genomic sectors may not contain significant amounts of repetitive DNAs other than the Sau3A family. A comparison between the chromosomal locations of Sau3A and EcoRI families of repeats has confirmed that each family is characterized by specific chromosomal locations and that single heterochromatic regions may contain both.

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Year:  1987        PMID: 3032768     DOI: 10.1007/BF00284102

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  31 in total

1.  Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome.

Authors:  J S Waye; H F Willard
Journal:  Nucleic Acids Res       Date:  1985-04-25       Impact factor: 16.971

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Journal:  Nat New Biol       Date:  1971-10-27

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Authors:  K W Jones; J Prosser; G Corneo; E Ginelli
Journal:  Chromosoma       Date:  1973-07-18       Impact factor: 4.316

4.  Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.

Authors:  J R Gosden; S S Lawrie; C M Gosden
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

5.  Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome.

Authors:  T P Yang; S K Hansen; K K Oishi; O A Ryder; B A Hamkalo
Journal:  Proc Natl Acad Sci U S A       Date:  1982-11       Impact factor: 11.205

6.  NOR associations with heterochromatin.

Authors:  C M Tuck-Muller; B L Bordson; M Varela; J W Bennett
Journal:  Cytogenet Cell Genet       Date:  1984

7.  Chromosomal localization of complex and simple repeated human DNAs.

Authors:  L Manuelidis
Journal:  Chromosoma       Date:  1978-03-22       Impact factor: 4.316

8.  Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.

Authors:  M E Harper; G F Saunders
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

9.  A satellite DNA isolated from human tissues.

Authors:  G Corneo; E Ginelli; E Polli
Journal:  J Mol Biol       Date:  1967-02-14       Impact factor: 5.469

10.  Organization and chromosomal specificity of autosomal homologs of human Y chromosome repeated DNA.

Authors:  R D Burk; P Szabo; S O'Brien; W G Nash; L Yu; K D Smith
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

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  17 in total

1.  A homologous subfamily of satellite III DNA on human chromosomes 14 and 22.

Authors:  K H Choo; E Earle; C McQuillan
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

2.  Genomic differentiation of 18S ribosomal DNA and beta-satellite DNA in the hominoid and its evolutionary aspects.

Authors:  H Hirai; T Taguchi; A K Godwin
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

3.  A chromosome 14-specific human satellite III DNA subfamily that shows variable presence on different chromosomes 14.

Authors:  K H Choo; E Earle; B Vissel; P Kalitsis
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

4.  The organisation of repetitive DNA sequences on human chromosomes with respect to the kinetochore analysed using a combination of oligonucleotide primers and CREST anticentromere serum.

Authors:  A Mitchell; P Jeppesen; D Hanratty; J Gosden
Journal:  Chromosoma       Date:  1992-03       Impact factor: 4.316

Review 5.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

6.  The organisation of repetitive sequences in the pericentromeric region of human chromosome 10.

Authors:  M S Jackson; P Slijepcevic; B A Ponder
Journal:  Nucleic Acids Res       Date:  1993-12-25       Impact factor: 16.971

7.  Differential digestion of the centromeric heterochromatic regions of the 5-azacytidine-decondensed human chromosomes 1, 9, 15, and 16 by NdeII and Sau3AI restriction endonucleases.

Authors:  P Martínez; C Bouza; A Viñas; L Sánchez
Journal:  Genetica       Date:  1995       Impact factor: 1.082

8.  Analysis of human extrachromosomal DNA elements originating from different beta-satellite subfamilies.

Authors:  G Assum; T Fink; T Steinbeisser; K J Fisel
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

9.  Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22.

Authors:  Y G Xie; F Y Han; S Bajalica; E Blennow; U Kristoffersson; J P Dumanski; M Nordenskjöld
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

10.  The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

Authors:  S T Winokur; U Bengtsson; J Feddersen; K D Mathews; B Weiffenbach; H Bailey; R P Markovich; J C Murray; J J Wasmuth; M R Altherr
Journal:  Chromosome Res       Date:  1994-05       Impact factor: 5.239

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