Literature DB >> 12043848

Genomic dissection reveals locus response to stress for mammalian acetylcholinesterase.

A D Grant1, M Shapira, H Soreq.   

Abstract

The mammalian acetylcholinesterase (ACHE) locus was investigated using computational predictive methods and experiments of reverse transcription polymerase chain reaction (RT-PCR). Computational analysis identified two genes downstream to ACHE, an inversely oriented arsenite resistance gene homologue (ARS), and a novel previously unidentified gene (PIX), co-oriented with ACHE. Experimental evidence shows coregulation of murine ACHE and ARS following confined swim, indicating coordinated locus response to stress, that is possibly mediated by altered cholinergic neurotransmission.

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Year:  2001        PMID: 12043848     DOI: 10.1023/a:1015112407079

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  31 in total

1.  Pesticide exposures and other agricultural risk factors for leukemia among men in Iowa and Minnesota.

Authors:  L M Brown; A Blair; R Gibson; G D Everett; K P Cantor; L M Schuman; L F Burmeister; S F Van Lier; F Dick
Journal:  Cancer Res       Date:  1990-10-15       Impact factor: 12.701

Review 2.  Non-classical actions of cholinesterases: role in cellular differentiation, tumorigenesis and Alzheimer's disease.

Authors:  P G Layer
Journal:  Neurochem Int       Date:  1996 May-Jun       Impact factor: 3.921

3.  Study of Alu sequences at the hypoxanthine phosphoribosyltransferase (hprt) encoding region of man.

Authors:  P J Renwick; A J Birley; M A Hultén
Journal:  Gene       Date:  1997-01-15       Impact factor: 3.688

4.  Anticholinesterases induce multigenic transcriptional feedback response suppressing cholinergic neurotransmission.

Authors:  D Kaufer; A Friedman; S Seidman; H Soreq
Journal:  Chem Biol Interact       Date:  1999-05-14       Impact factor: 5.192

5.  A transcription-activating polymorphism in the ACHE promoter associated with acute sensitivity to anti-acetylcholinesterases.

Authors:  M Shapira; I Tur-Kaspa; L Bosgraaf; N Livni; A D Grant; D Grisaru; M Korner; R P Ebstein; H Soreq
Journal:  Hum Mol Genet       Date:  2000-05-22       Impact factor: 6.150

6.  Expression cloning for arsenite-resistance resulted in isolation of tumor-suppressor fau cDNA: possible involvement of the ubiquitin system in arsenic carcinogenesis.

Authors:  T G Rossman; Z Wang
Journal:  Carcinogenesis       Date:  1999-02       Impact factor: 4.944

7.  Acute stress facilitates long-lasting changes in cholinergic gene expression.

Authors:  D Kaufer; A Friedman; S Seidman; H Soreq
Journal:  Nature       Date:  1998-05-28       Impact factor: 49.962

Review 8.  Resistance mechanisms to arsenicals and antimonials.

Authors:  B P Rosen
Journal:  J Basic Clin Physiol Pharmacol       Date:  1995

Review 9.  Acetylcholinesterase: C-terminal domains, molecular forms and functional localization.

Authors:  J Massoulié; A Anselmet; S Bon; E Krejci; C Legay; N Morel; S Simon
Journal:  J Physiol Paris       Date:  1998 Jun-Aug

10.  Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in mice.

Authors:  R Beeri; C Andres; E Lev-Lehman; R Timberg; T Huberman; M Shani; H Soreq
Journal:  Curr Biol       Date:  1995-09-01       Impact factor: 10.834

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