Literature DB >> 8641690

EagI and NotI linking clones from human chromosomes 11 and Xp.

M A Pook1, R Thakrar, B Pottinger, B Harding, D Porteous, V van Heyningen, J Cowell, C Jones, S Povey, K E Davies, R V Thakker.   

Abstract

EagI and NotI linking libraries were prepared in the lambda vector, EMBL5, from the mouse-human somatic cell hybrid 1W1LA4.9, which contains human chromosomes 11 and Xp as the only human component. Individual clones containing human DNA were isolated by their ability to hybridise with total human DNA and digested with SalI and EcoRI to identify the human insert size and single-copy fragments. The mean (+/- SD) insert sizes of the EagI and NotI clones were 18.3 +/- 3.2 kb and 16.6 +/- 3.6 kb, respectively. Regional localisation of 66 clones (52 EagI, 14 NotI) was achieved using a panel of 20 somatic cell hybrids that contained different overlapping deletions of chromosomes 11 or Xp. Thirty-nine clones (36 EagI, 3 NotI) were localised to chromosome 11; 17 of these were clustered in 11q13 and another nine were clustered in 11q14-q23.1. Twenty-seven clones (16 EagI, 11 NotI) were localised to Xp and 10 of these were clustered in Xp11. The 66 clones were assessed for seven different microsatellite repetitive sequences; restriction fragment length polymorphisms for five clones from 11q13 were also identified. These EagI and NotI clones, which supplement those previously mapped to chromosome 11 and Xp, should facilitate the generation of more detailed maps and the identification of genes that are associated with CpG-rich islands.

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Year:  1996        PMID: 8641690     DOI: 10.1007/BF02346183

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


  41 in total

1.  Characterization of (CA)n microsatellites with degenerate sequencing primers.

Authors:  D L Browne; M Litt
Journal:  Nucleic Acids Res       Date:  1992-01-11       Impact factor: 16.971

2.  Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library.

Authors:  R B Wadey; P F Little; J Pritchard; J K Cowell
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

3.  A human chromosome 11 NotI end clone library.

Authors:  J Sanford; B W Kim; L L Deaven; C Jones; M J Higgins; N J Nowak; T B Shows
Journal:  Genomics       Date:  1993-03       Impact factor: 5.736

4.  Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994.

Authors:  H F Willard; F Cremers; J L Mandel; A P Monaco; D L Nelson; D Schlessinger
Journal:  Cytogenet Cell Genet       Date:  1994

5.  Further studies on a hybrid cell-surface antigen associated with human chromosome 11 using a monoclonal antibody.

Authors:  C Jones; K A Kimmel; T E Carey; Y E Miller; D W Lehman; D MacKenzie
Journal:  Somatic Cell Genet       Date:  1983-07

6.  Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

Authors:  R V Thakker; P Bouloux; C Wooding; K Chotai; P M Broad; N K Spurr; G M Besser; J L O'Riordan
Journal:  N Engl J Med       Date:  1989-07-27       Impact factor: 91.245

7.  The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.

Authors:  J K Cowell; R B Wadey; B B Buckle; J Pritchard
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

8.  Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Authors:  P Wieacker; K E Davies; H J Cooke; P L Pearson; R Williamson; S Bhattacharya; J Zimmer; H H Ropers
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids.

Authors:  D S Gerhard; E Lawrence; J Wu; H Chua; N Ma; S Bland; C Jones
Journal:  Genomics       Date:  1992-08       Impact factor: 5.736

10.  Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Authors:  S J Scheinman; M A Pook; C Wooding; J T Pang; P A Frymoyer; R V Thakker
Journal:  J Clin Invest       Date:  1993-06       Impact factor: 14.808

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  1 in total

1.  Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Authors:  J T Pang; S E Lloyd; C Wooding; B Farren; B Pottinger; B Harding; S E Leigh; M A Pook; F J Benham; G T Gillett; R T Taggart; R V Thakker
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

  1 in total

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