Literature DB >> 1783377

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.

M S Driesen1, J G Dauwerse, M C Wapenaar, E J Meershoek, P Mollevanger, K L Chen, K H Fischbeck, G J van Ommen.   

Abstract

A yeast artificial chromosome (YAC) library has been constructed from a somatic cell hybrid containing a t(1p;19q) chromosome and chromosome 17. After amplification, part of this library was analyzed by high-density colony filter screening with a repetitive human DNA probe (Alu). The human YACs distinguished by the screening were further analyzed by Alu fingerprinting and Alu PCR. Fluorescent in situ hybridization (FISH) was performed to localize the YACs to subchromosomal regions of chromosome 1p, 17, or 19q. We have obtained a panel of 123 individual YACs with a mean size of 160 kb, and 77 of these were regionally localized by FISH: 33 to 1p, 10 to 17p, 25 to 17q, and 9 to 19q. The YACs cover a total of 19.7 Mb or 9% of the 220 Mb of human DNA contained in the hybrid. No overlapping YACs have yet been detected. These YACs are available upon request and should be helpful in mapping studies of disease loci, e.g., Charcot-Marie-Tooth disease, Miller-Dieker syndrome, hereditary breast tumor, myotonic dystrophy, and malignant hyperthermia.

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Year:  1991        PMID: 1783377     DOI: 10.1016/0888-7543(91)90035-d

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  A transcribed polymorphism and sub-localisation of MDM2.

Authors:  J Heighway; E L Mitchell; D Jones; G R White; M F Santibáñez Koref
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

2.  Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations.

Authors:  F Petrij; H G Dauwerse; R I Blough; R H Giles; J J van der Smagt; R Wallerstein; P D Maaswinkel-Mooy; C D van Karnebeek; G J van Ommen; A van Haeringen; J H Rubinstein; H M Saal; R C Hennekam; D J Peters; M H Breuning
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

3.  A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene.

Authors:  J A Terrett; R Newbury-Ecob; N M Smith; Q Y Li; C Garrett; P Cox; D Bonnet; S Lyonnet; A Munnich; A J Buckler; J D Brook
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

4.  Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.

Authors:  J F Deleuze; S Dhorne; J Hazan; E Borghi; N Raynaud; N Pollet; M Meunier-Rotival; J Deschatrette; D Alagille; M Hadchouel
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

5.  Construction and characterization of a bacterial artificial chromosome library of Sorghum bicolor.

Authors:  S S Woo; J Jiang; B S Gill; A H Paterson; R A Wing
Journal:  Nucleic Acids Res       Date:  1994-11-25       Impact factor: 16.971

6.  Intrachromosomal triplication of 15q11-q13.

Authors:  A A Schinzel; L Brecevic; F Bernasconi; F Binkert; F Berthet; A Wuilloud; W P Robinson
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

  6 in total

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