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1.
Am J Respir Crit Care Med ; 187(6): 584-8, 2013 Mar 15.
Article in English | MEDLINE | ID: mdl-23328528

ABSTRACT

RATIONALE: Epigenetic and/or genetic variation in the gene encoding the receptor for adenylate-cyclase activating polypeptide 1 (ADCYAP1R1) has been linked to post-traumatic stress disorder in adults and anxiety in children. Psychosocial stress has been linked to asthma morbidity in Puerto Rican children. OBJECTIVES: To examine whether epigenetic or genetic variation in ADCYAP1R1 is associated with childhood asthma in Puerto Ricans. METHODS: We conducted a case-control study of 516 children ages 6-14 years living in San Juan, Puerto Rico. We assessed methylation at a CpG site in the promoter of ADCYAP1R1 (cg11218385) using a pyrosequencing assay in DNA from white blood cells. We tested whether cg11218385 methylation (range, 0.4-6.1%) is associated with asthma using logistic regression. We also examined whether exposure to violence (assessed by the Exposure to Violence [ETV] Scale in children 9 yr and older) is associated with cg11218385 methylation (using linear regression) or asthma (using logistic regression). Logistic regression was used to test for association between a single nucleotide polymorphism in ADCYAP1R1 (rs2267735) and asthma under an additive model. All multivariate models were adjusted for age, sex, household income, and principal components. MEASUREMENTS AND MAIN RESULTS: EACH 1% increment in cg11218385 methylation was associated with increased odds of asthma (adjusted odds ratio, 1.3; 95% confidence interval, 1.0-1.6; P = 0.03). Among children 9 years and older, exposure to violence was associated with cg11218385 methylation. The C allele of single nucleotide polymorphism rs2267735 was significantly associated with increased odds of asthma (adjusted odds ratio, 1.3; 95% confidence interval, 1.02-1.67; P = 0.03). CONCLUSIONS: Epigenetic and genetic variants in ADCYAP1R1 are associated with asthma in Puerto Rican children.


Subject(s)
Asthma/genetics , Genetic Variation/genetics , Hispanic or Latino/genetics , Adolescent , Case-Control Studies , Child , CpG Islands/genetics , DNA Methylation/genetics , Epigenesis, Genetic , Female , Humans , Logistic Models , Male , Polymorphism, Single Nucleotide , Puerto Rico/ethnology , Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide
2.
PLoS One ; 7(12): e52190, 2012.
Article in English | MEDLINE | ID: mdl-23251700

ABSTRACT

Kremens are high-affinity receptors for Dickkopf 1 (Dkk1) and regulate the Wnt/ß-catenin signaling pathway by down-regulating the low-density lipoprotein receptor-related protein 6 (LRP6). Dkk1 competes with Wnt for binding to LRP6; binding of Dkk1 inhibits canonical signaling through formation of a ternary complex with Kremen. The majority of down-regulated clathrin-mediated endocytic receptors contain short conserved regions that recognize tyrosine or dileucine sorting motifs. In this study, we found that Kremen1 is internalized from the cell surface in a clathrin-dependent manner. Kremen1 contains an atypical dileucine motif with the sequence DXXXLV. Mutation of LV to AA in this motif blocked Kremen1 internalization; as reported previously for other proteins, the aspartic acid residue in Kremen1 is not critical. Inhibition of expression of the adaptor protein 2 (AP-2) or inhibition of clathrin by pitstop 2 also blocked Kremen1 internalization. The novel amino acid sequence identified in Kremen1 is similar to the motif previously identified in hydra, yeast, and other organisms known to signal from the trans-Golgi network to the endosomal compartment.


Subject(s)
Clathrin/metabolism , Intercellular Signaling Peptides and Proteins/metabolism , Adaptor Protein Complex 2/genetics , Adaptor Protein Complex 2/metabolism , Amino Acid Motifs , Amino Acid Sequence , Animals , Cell Line , Cell Line, Tumor , Cell Membrane/genetics , Cell Membrane/metabolism , Clathrin/genetics , Endocytosis , HEK293 Cells , HeLa Cells , Humans , Intercellular Signaling Peptides and Proteins/genetics , Mice , Molecular Sequence Data , Mutation , Protein Binding , Protein Transport , Sequence Alignment
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