Literature DB >> 2777253

Mapping studies of the serum cholinesterase-2 locus (CHE2).

M L Marazita1, B J Keats, M A Spence, R S Sparkes, L L Field, M C Sparkes, M Crist.   

Abstract

Serum cholinesterase (butyrylcholinesterase, EC 3.1.1.8, BChE) is controlled by two genetic loci, CHE1 and CHE2. The CHE1 locus has been mapped to 3q, but the map location of CHE2 is uncertain. In an effort to clarify the location of CHE2, we combined all the published linkage analysis data for CHE2 (as summarized in the Keats Linkage Database) with the data from the UCLA Linkage Database. Exclusions with substantial portions of the genome could be made (notably with portions of chromosomes 1, 2, 3, 4, 6, 7, 8, 9, 14, 16, 18, 19, 20, 22, and LG1). Although not quite statistically significant (zeta = 2.51), loose linkage (theta = 0.32) of CHE2 with the haptoglobin locus on 16q22 was the most likely conclusion from the family data. In addition, calculating the lod score between CHE2 and the available linkage map of chromosome 16 (markers HBA, PGP, FRA16A, and HP) resulted in an overall lod score of 3.2. This result is particularly intriguing given the hybridization of a BChE cDNA (designated CHEL3) to the same region. Resolution of the issue will require more detailed linkage studies of CHE2 on chromosome 16 and a better understanding of the relationship between the CHE1 and CHE2 loci with respect to production of serum cholinesterases.

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Year:  1989        PMID: 2777253     DOI: 10.1007/BF00286706

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


  28 in total

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3.  Linkage relationships between 22 autosomal markers.

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4.  Genetic variation in human erythrocyte acetylcholinesterase.

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5.  A chiasma map of man.

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Review 6.  On the geographical distribution of pseudocholinesterase variants.

Authors:  H Steegmüller
Journal:  Humangenetik       Date:  1975

7.  Genetic linkage relation to the pepsinogen Pg5 locus.

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8.  Isolation and characterization of full-length cDNA clones coding for cholinesterase from fetal human tissues.

Authors:  C A Prody; D Zevin-Sonkin; A Gnatt; O Goldberg; H Soreq
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

9.  Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22.

Authors:  H Eiberg; N Møller; J Mohr; L S Nielsen
Journal:  Clin Genet       Date:  1986-05       Impact factor: 4.438

10.  Linkage of plasma alpha-L-fucosidase (FUCA2) and the plasminogen (PLG) system.

Authors:  H Eiberg; J Mohr; L S Nielsen
Journal:  Clin Genet       Date:  1984-07       Impact factor: 4.438

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  1 in total

1.  Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.

Authors:  B N La Du; C F Bartels; C P Nogueira; M Arpagaus; O Lockridge
Journal:  Cell Mol Neurobiol       Date:  1991-02       Impact factor: 5.046

  1 in total

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