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Acetylcholinesterase Paraoxonase Genotype and Expression Predict Acetylcholinesterase͞paraoxonase genotype and expression predict anxiety scores in Health, Risk Factors, Exercise Training, and Genetics study Ella H. Sklan*, Alexander Lowenthal*, Mira Korner†, Ya’acov Ritov‡, Daniel M. Landers§, Tuomo Rankinen¶, Claude Bouchard¶, Arthur S. Leonʈ, Treva Rice**, D. C. Rao**, Jack H. Wilmore††, James S. Skinner‡‡, and Hermona Soreq*§§ *Department of Biological Chemistry and †Laboratory of DNA Analysis, ‡Institute of Life Sciences and Department of Statistics, Hebrew University of Jerusalem, Jerusalem 91904, Israel; §Department of Kinesiology, Arizona State University, Tempe, AZ 85287; ¶Human Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA 70808; ʈSchool of Kinesiology and Leisure Studies, University of Minnesota, Minneapolis, MN 55455; **Division of Biostatistics, Washington University School of Medicine, St. Louis, MO 63110; ††Department of Health and Kinesiology, Texas A&M University, College Station, TX 78363; and ‡‡Department of Kinesiology, Indiana University, Bloomington, IN 47405 Edited by Roger D. Kornberg, Stanford University School of Medicine, Stanford, CA, and approved February 23, 2004 (received for review November 19, 2003) Anxiety involves complex, incompletely understood interactions of chemical warfare agents, depletes both AChE and the homol- genomic, environmental, and experience-derived factors, and is ogous enzyme butyrylcholinesterase (BChE) (11), inducing cho- currently being measured by psychological criteria. Here, we report linergic excitation. Polymorphisms in the corresponding ACHE previously nonperceived interrelationships between expression and BCHE genes could hence affect both the environmental and variations and nucleotide polymorphisms of the chromosome the experience-related elements of anxiety. A third relevant 7q21–22 acetylcholinesterase-paraoxonase 1 (ACHE-PON1) locus enzyme is the PON protein product of the paraoxonase PON1 with the trait- and state-anxiety measures of 461 healthy subjects gene, which destroys environmental toxins that target AChE from the Health, Risk Factors, Exercise Training, and Genetics (12). PON also possesses peroxidase-like activity (13), and can Family Study. The AChE protein controls the termination of the directly reduce oxidative stress in macrophages and in serum stress-enhanced acetylcholine signaling, whereas the PON protein (14). Polymorphisms in the ACHE, BCHE, and PON1 genes displays peroxidase-like activity, thus protecting blood proteins could therefore affect both the environmental and the experi- from oxidative stress damages. Serum AChE and PON enzyme ence-related elements of anxiety. activities were both found to be affected by demographic param- In mice, we observed that acute stress of even moderate eters, and showed inverse, reciprocal associations with anxiety intensity (e.g., confined swim) causes modulation of the genetic measures. Moreover, the transient scores of state anxiety and the regulation of ACh availability in the CNS (15). This condition susceptibility score of trait anxiety both appeared to be linked to may be viewed as a laboratory-induced passive gene– enzyme activities. This finding supported the notion of correspond- environment interaction, demonstrating that environmental ing gene expression relationships. Parallel polymorphisms in the components of variance for anxiety measures are experience ACHE and PON1 genes displayed apparent associations with both related, and vice versa. This gene–environment interaction in- trait- and state-anxiety scores. Our findings indicate that a signif- volves overproduction of the readthrough monomeric AChE icant source of anxiety feelings involves inherited and acquired (AChE-R) splice variant. Such overproduction acts in the short parameters of acetylcholine regulation that can be readily quan- term to reduce excess ACh after stress, but at a longer term, is tified, which can help explaining part of the human variance for associated with glucocorticoid-regulated neuronal hyperarousal state and trait anxiety. and extreme sensitivity to anti-AChEs (16). Transgenic overex- pression of AChE-R in mice intensifies conflict behavior (17), nxiety is a ubiquitous and unavoidable experience of life, another phenomenon associated with anxiety (18). In view of Adefined as a feeling of fear that is out of proportion to the these findings, we initiated a study aimed at testing whether nature of the threat (1). Anxiety disorders are the most prevalent genomic polymorphisms in the ACHE-PON1 locus and corre- of psychiatric disorders (2), which led to an extensive search of sponding changes in serum AChE, BChE, and PON activities the mechanisms and͞or genomic elements underlying these could serve as predictors of the anxiety scores of healthy phenomena. Several genes were reported to be potential con- humans, assisting the study of this complex phenotype. tributors to the genetic variance of anxiety-related traits or Materials and Methods modifiers of the phenotypic expression of pathologic anxiety (3). However, molecular genetics and͞or biochemistry have so far Study Sample Description. The Health, Risk Factors, Exercise failed to identify variation(s) that are consistently associated Training, and Genetics (HERITAGE) Family Study was de- with the increased psychologically measurable susceptibility to signed to investigate the role of diverse risk factors in the anxiety feelings in generally healthy subjects. genotype on responses to regular exercise (19). Measures of state Variance in personality traits is often considered to involve and trait anxiety were obtained on a subset of the families as part complex interactions of environmental and experience-derived factors with several gene products and neurotransmission cir- This paper was submitted directly (Track II) to the PNAS office. cuits [e.g., serotonergic (4), GABAergic, and cholinergic (5)]. Abbreviations: ACh, acetylcholine; AChE, acetylcholinesterase; AChE-R, readthrough Neurotransmission mediated by acetylcholine (ACh) in partic- AChE; PON, paraoxonase; BChE, butyrylcholinesterase; HERITAGE, Health, Risk Factors, ular contributes to numerous physiologic functions (6) as well as Exercise Training, and Genetics; LD, linkage disequilibrium; STAI, state-trait-anxiety inven- to memory, learning, and panic responses (7, 8). Anxiety pro- tory; BMI, body mass index. vokes cholinergic hyperarousal (e.g., sweating, intestinal or Data deposition: The sequences reported in this paper have been deposited in the GenBank gastric constrictions, etc.) (9, 10). In addition, the ACh hydro- database [accession nos. AF539592 (PON1), AF002993 (ACHE), and NM000055 (BCHE)]. lyzing enzyme acetylcholinesterase (AChE) is a target of pesti- §§To whom correspondence should be addressed. E-mail: [email protected]. cides. Human exposure to pesticides, or to the closely related © 2004 by The National Academy of Sciences of the USA 5512–5517 ͉ PNAS ͉ April 13, 2004 ͉ vol. 101 ͉ no. 15 www.pnas.org͞cgi͞doi͞10.1073͞pnas.0307659101 Downloaded by guest on October 1, 2021 of the study questionnaire. A total of 461 individuals (198 men and 263 women) from 150 two-generation families of African- American (172) or Caucasian origin (289) with complete data were available for this study. Serum Analyses. Blood samples were collected at baseline in the morning after a 12-h fast. Questionnaires were completed later that morning. Serum was prepared by blood centrifugation at 2,000 ϫ g (15 min at 4°C). Aliquots of 2 ml in cryogenic tubes were frozen at 80°C until use. Nondenaturing gel and catalytic activity measurements of AChE were as described (15). For other enzyme tests, see Supporting Materials and Methods, which is published as supporting information on the PNAS web site. Genotyping. Genomic DNA was prepared from permanent lym- phoblastoid cells as described (20). PCR amplification by using Taq polymerase (Sigma, D-6677) was followed by Exo-Sap enzymatic purification (United States Biochemical, US78200) of the PCR product (Table 1, which is published as supporting information on the PNAS web site). Standard automated se- quencing was performed by using the Big Dye Terminator cycle sequencing chemistry, ABI 3700 DNA analyzer, and data col- lection and sequence analysis software (Applied Biosystems). The 55L͞M and 192Q͞R coding sequence polymorphisms in PON1 were detected by using single-nucleotide primer extension and the SNaPshot method (SNaPshot ddNTP primer extension kit, ABI), using as probes 5Ј-GGCAGAAACTGG CTCTGAA- GAC-3Ј for 55L͞M and 5Ј-GATCACTATTTTCTTGAC- CCCTACTTAC-3Јfor 192Q͞R. After extension and calf intes- tine phosphatase treatment (Amersham Pharmacia Biosciences, Freiburg, Germany, E2250Y), products were electrophoresed on a 3700 ABI analyzer and results were analyzed with GENESCAN software. Statistics. To test whether observed genotype frequencies con- Fig. 1. Acquired changes in measured values. Graphs show mean Ϯ SEM for BIOCHEMISTRY formed with the Hardy–Weinberg equilibrium expectations, and each value (n ϭ 434). Note that trait-anxiety scores decrease with age, whereas to evaluate the significance of the linkage disequilibrium (LD) AChE and BChE activities are elevated with both age and BMI. between each polymorphism pair, we used the ␹2 test. P values for the difference between the genotypes of the subjects in distinct trait anxiety subgroups were calculated by the state-trait-anxiety inventory (STAI) (25). To investigate the using the likelihood ratio test. The P value was the exact role of cholinergic
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