Literature DB >> 6205826

Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes.

D M Kurnit, R L Neve, C C Morton, G A Bruns, N S Ma, D R Cox, H P Klinger.   

Abstract

A search for genes located on human chromosome 21 resulted in the isolation of a HeLa cDNA clone, pUNC724, which hybridized to 3.7 and 2.5 kilobase (kb) EcoRI fragments on each of the human acrocentric chromosomes. In situ hybridization further localized pUNC724 to the pericentromeric region of the human acrocentrics. Two other EcoRI fragments that hybridized to pUNC724 were assigned to the long arms of chromosomes 1 and 18. The pUNC724 sequence does not appear to be related to ribosomal or satellite DNA sequences. The juxtaposition of DNA sequences homologous to pUNC724 and ribosomal DNA sequences presumably occurred within the past thirty-five million years, following the divergence of the lines leading to man and the New World owl monkey, Aotus trivirgatus--pUNC724 is not syntenic with the single chromosome containing ribosomal DNA sequences in the owl monkey.

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Year:  1984        PMID: 6205826     DOI: 10.1159/000132039

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  13 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

2.  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

Review 3.  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

4.  Cytochemical heterogeneity of the C-band in human chromosome 1.

Authors:  A Babu; R S Verma
Journal:  Histochem J       Date:  1986-06

5.  Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes.

Authors:  U Tantravahi; G D Stewart; M Van Keuren; G McNeil; S Roy; D Patterson; H Drabkin; M Lalande; D M Kurnit; S A Latt
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

6.  Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

Authors:  G D Stewart; T J Hassold; A Berg; P Watkins; R Tanzi; D M Kurnit
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

7.  Regional localization and characterization of a DNA segment on the long arm of chromosome 21.

Authors:  D N Cooper; S C Niemann; J R Gosden; A R Mitchell; A M Goate; G S Rajendran; D A Miller; L Lim; J Schmidtke
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

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.  Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes.

Authors:  R Viersbach; G Schwanitz; M M Nöthen
Journal:  Hum Genet       Date:  1994-06       Impact factor: 4.132

10.  Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19. Two animal models for human trisomies.

Authors:  C Bacchus; H Sterz; W Buselmaier; S Sahai; H Winking
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

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