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PMID: 2828023 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'.

The EMBO journal ·Vol. 6 ·No. 11 ·1987-11-00 ·Pages 3285-9

Nguyen C, Pontarotti P, Birnbaum D, Chimini G, Rey JA, Mattei JF, Jordan BR

Abstract

In spite of the large amount of genetic data obtained on the X chromosome and of the availability of many cloned sequences little is known about the physical map of this chromosome. The construction of large-scale restriction maps is now possible with pulsed field gel methods and data has recently been obtained in the region of band Xq28. We present here results of physical mapping in the Xq27 region, i.e. proximal to the fragile site at Xq27.3 associated with mental retardation, and show physical linkage between the coagulation factor IX gene and the mcf.2 transforming sequence recently localized to Xq27. Our data also indicate partial methylation of some sites in this region, and locate several 'HTF islands', i.e. CpG-rich, unmethylated sequences, containing several sites for 'rare cutter' enzymes, which are believed to be associated with expressed 'housekeeping' genes.

MeSH Terms
Base Composition Cell Line Chromosome Mapping DNA Restriction Enzymes Factor IX/genetics Fragile X Syndrome Genes Humans Hybrid Cells/cytology Male Nucleic Acid Hybridization Sex Chromosome Aberrations Transformation, Genetic Translocation, Genetic X Chromosome
Chemicals
Factor IX DNA Restriction Enzymes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Nguyen C
Centre d'Immunologie INSERM-CNRS de Marseille-Luminy, France.
Pontarotti P
Birnbaum D
Chimini G
Rey J A
Mattei J F
Jordan B R
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16 references, click to expand
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1987-11-00
Pages
3285-9
Language
English
Region
England
NLM ID
8208664
PMCID
PMC553781
Subset
IM
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