Literature DB >> 8531924

Assignment of Alu-repetitive sequences to large restriction fragments from human chromosomes 6 and 22.

E Meese1, H W Müller, N Brass, J M Trent, N Blin.   

Abstract

We have employed a pulsed field gel electrophoresis and Alu hybridization approach for identification of large restriction fragments on chromosome 6 and 22. This technique allows large portions of selected human chromosomes to be visualized as discrete hybridization signals. Somatic cell hybrid DNA which contains chromosome 6 or chromosome 22 was restricted with either Notl or Mlul. The restriction fragments were separated by pulsed field gel electrophoresis (PFGE) and hybridized against an Alu repetitive sequence (Blur 8). The hybridization signals result in a fingerprint-like pattern which is unique for each chromosome and each restriction enzyme. In addition, a continuous pattern of restriction fragments was demonstrated by gradually increasing puls times. This approach will also be suitable to analyze aberrant human chromosomes retained in somatic cell hybrids and can be used to analyze flow sorted human chromosomes. To this end, our method provides a valuable alternative to standard cytogenetic analysis.

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Year:  1995        PMID: 8531924     DOI: 10.1007/bf00986496

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  20 in total

1.  Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.

Authors:  O Delattre; J Zucman; B Plougastel; C Desmaze; T Melot; M Peter; H Kovar; I Joubert; P de Jong; G Rouleau
Journal:  Nature       Date:  1992-09-10       Impact factor: 49.962

2.  A centromere-based genetic map of the short arm of human chromosome 6.

Authors:  H Blanché; H Y Zoghbi; E W Jabs; B de Gouyon; R Zunec; J Dausset; H M Cann
Journal:  Genomics       Date:  1991-03       Impact factor: 5.736

3.  Development and utilization of a somatic cell hybrid mapping panel to assign NotI linking probes to the long arm of human chromosome 6.

Authors:  E U Meese; C M Witkowski; H Y Zoghbi; E J Stanbridge; P S Meltzer; J M Trent
Journal:  Genomics       Date:  1992-03       Impact factor: 5.736

4.  Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR.

Authors:  B L Dubois; S L Naylor
Journal:  Genomics       Date:  1993-05       Impact factor: 5.736

5.  Report and abstracts of the Fourth International Workshop on Human Chromosome 22 mapping 1994. Cambridge, United Kingdom, July 2-4, 1994.

Authors:  P J Scambler
Journal:  Cytogenet Cell Genet       Date:  1994

6.  A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors:  A de la Chapelle; R Herva; M Koivisto; P Aula
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 7.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

8.  NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.

Authors:  H L Drwinga; L H Toji; C H Kim; A E Greene; R A Mulivor
Journal:  Genomics       Date:  1993-05       Impact factor: 5.736

9.  The human Y chromosome: a 43-interval map based on naturally occurring deletions.

Authors:  D Vollrath; S Foote; A Hilton; L G Brown; P Beer-Romero; J S Bogan; D C Page
Journal:  Science       Date:  1992-10-02       Impact factor: 47.728

10.  Tumorigenicity in human melanoma cell lines controlled by introduction of human chromosome 6.

Authors:  J M Trent; E J Stanbridge; H L McBride; E U Meese; G Casey; D E Araujo; C M Witkowski; R B Nagle
Journal:  Science       Date:  1990-02-02       Impact factor: 47.728

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