Literature DB >> 2788606

Toward a long-range map of human chromosomal band 22q11.

H E McDermid1, M L Budarf, B S Emanuel.   

Abstract

Human chromosome band 22q11 is involved in numerous chromosomal rearrangements. A long-range molecular map of this region would allow the more precise localization of the various breakpoints of these rearrangements. Toward this goal we have constructed a genomic DNA library that allows the isolation of DNA clones that are directly adjacent to NotI sites. NotI was chosen because it is a restriction enzyme that digests infrequently in the human genome. The genomic DNA used in this library was from a human/hamster hybrid cell line that has a chromosome 22 as the only visible human chromosome. Two clones were isolated and mapped to different regions of 22q11 using a somatic cell hybrid mapping panel. A long-range restriction map flanking the NotI site of each of these two clones was produced using NotI and other infrequently cutting enzymes. Both NotI sites analyzed were located in HTF islands, regions often associated with the 5' end of genes. Thus, the NotI map of 22q11 may also aid in the cloning of undiscovered genes, giving a starting point for the study of duplication/deficiency syndromes of the region.

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Year:  1989        PMID: 2788606     DOI: 10.1016/0888-7543(89)90079-7

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


  7 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  Mapping of the human lambda immunoglobulin variable gene subgroup 1.

Authors:  H E McDermid; B S Emanuel
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

3.  Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2.

Authors:  T R Bauer; H E McDermid; M L Budarf; M L Van Keuren; B B Blomberg
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

4.  Molecular characterization of the marker chromosome associated with cat eye syndrome.

Authors:  A J Mears; A M Duncan; M L Budarf; B S Emanuel; B Sellinger; J Siegel-Bartelt; C R Greenberg; H E McDermid
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

5.  Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183).

Authors:  M P Mulder; M Wilke; A Langeveld; L G Wilming; A Hagemeijer; E van Drunen; E C Zwarthoff; P H Riegman; W H Deelen; A M van den Ouweland
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

6.  Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

Authors:  E Goldmuntz; D Driscoll; M L Budarf; E H Zackai; D M McDonald-McGinn; J A Biegel; B S Emanuel
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

7.  Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.

Authors:  H Kurahashi; K Akagi; K Karakawa; T Nakamura; J P Dumanski; T Sano; S Okada; S Takai; I Nishisho
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

  7 in total

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