Literature DB >> 3701863

Sequence relationships of three human satellite DNAs.

J Prosser, M Frommer, C Paul, P C Vincent.   

Abstract

The simple sequence components of three human classical satellite DNAs have been defined, and some segments of each satellite have been sequenced. Each of the classical satellites I, II and III was found to contain, as a major component, a single family of simple repeated sequences. The three simple-sequence families have been called satellites 1, 2 and 3, to indicate the enrichment of each in one of the classical satellites I, II and III, and to differentiate them from these classical satellites, which also contain other repeated components. Satellite 3, the simple sequence component of classical satellite III, when digested with the restriction endonuclease HinfI, forms a ladder based on a repeat of five base-pairs, 5' A-T-T-C-C. The HinfI ladder was shown to be composed of repeated elements with the general sequence 5' (A-T-T-C-C)n-A-TC-T-C-G-G-G-T-T-G. Satellite 2, the simple sequence component of classical satellite II, is digested by HinfI into a large number of very small fragments, of length 10 to 80 base-pairs. These were found to contain the simple repeat 5' A-T-T-C-C, in a highly diverged form. Analysis of satellite 2 sequences suggested that the five base-pair repeat was originally amplified as a higher-order repeat like that of satellite 3. However, the main tandemly repeated segments of satellite 2 in the human genome are much longer, and the simple sequence elements on which they are based are quite degenerate. Satellite 1, the simple sequence component of classical satellite I, is digested by the restriction endonuclease RsaI into a ladder of fragments less than 150 base-pairs in length. These ladder fragments were found to be formed by the loss of RsaI sites from two related A + T-rich sequences, A (17 base-pairs) and B (25 base-pairs), arranged in alternating arrays, -A-B-A-B-A-. Analysis of a large number of cloned fragments from the RsaI ladder of satellite 1 showed that the tandem arrays, -A-B-A-B-A, have a more complex arrangement, with apparent amplification of segments containing particular sequence variants of the repeat units, A and B. No sequence relationship was evident between the repeat elements of satellite 1 and those of satellites 2 and 3.

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Year:  1986        PMID: 3701863     DOI: 10.1016/0022-2836(86)90224-x

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  63 in total

1.  Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.

Authors:  R Bandyopadhyay; C McQuillan; S L Page; K H Choo; L G Shaffer
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

Review 2.  Unusual DNA duplex and hairpin motifs.

Authors:  Shan-Ho Chou; Ko-Hsin Chin; Andrew H-J Wang
Journal:  Nucleic Acids Res       Date:  2003-05-15       Impact factor: 16.971

3.  Antibodies to defined histone epitopes reveal variations in chromatin conformation and underacetylation of centric heterochromatin in human metaphase chromosomes.

Authors:  P Jeppesen; A Mitchell; B Turner; P Perry
Journal:  Chromosoma       Date:  1992-03       Impact factor: 4.316

Review 4.  Code domains in tandem repetitive DNA sequence structures.

Authors:  P Vogt
Journal:  Chromosoma       Date:  1992-10       Impact factor: 4.316

5.  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

6.  Dodeca satellite: a conserved G+C-rich satellite from the centromeric heterochromatin of Drosophila melanogaster.

Authors:  J P Abad; M Carmena; S Baars; R D Saunders; D M Glover; P Ludeña; C Sentis; C Tyler-Smith; A Villasante
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

7.  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

8.  Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.

Authors:  Robert Lyle; Paola Prandini; Kazutoyo Osoegawa; Boudewijn ten Hallers; Sean Humphray; Baoli Zhu; Eduardo Eyras; Robert Castelo; Christine P Bird; Sarantos Gagos; Carol Scott; Antony Cox; Samuel Deutsch; Catherine Ucla; Marc Cruts; Sophie Dahoun; Xinwei She; Frederique Bena; Sheng-Yue Wang; Christine Van Broeckhoven; Evan E Eichler; Roderic Guigo; Jane Rogers; Pieter J de Jong; Alexandre Reymond; Stylianos E Antonarakis
Journal:  Genome Res       Date:  2007-09-25       Impact factor: 9.043

9.  Highly conserved repetitive DNA sequences are present at human centromeres.

Authors:  D L Grady; R L Ratliff; D L Robinson; E C McCanlies; J Meyne; R K Moyzis
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

10.  A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

Authors:  L E Voullaire; H R Slater; V Petrovic; K H Choo
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

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