Association between genome-wide association studies reported SNPs and pediatric-onset Crohn’s disease in Canadian children

A recent pediatric-focused genome-wide association study has implicated three novel susceptibility loci for Crohn’ disease (CD).We aimed to investigate whether the three recently reported and other previously reported genes/loci were also associated with CD in Canadian children. A case–control design was implemented at three pediatric gastroenterology clinics in Canada. Children <19 years of age with a confirmed diagnosis of CD were recruited along with controls. Single nucleotide polymorphisms (SNPs) in 19 reported genes/loci were genotyped. Associations between individual SNPs and CD were examined. A total of 563 cases and 553 controls were studied. The mean (±SD) age of the cases was 12.3 (±3.2) years. Most cases were male (56.0%), had ileo-colonic disease (L3 ± L4, 48.8%) and inflammatory behavior (B1 ± p, 87.9%) at diagnosis. Allelic association analysis (two-tailed) showed that 8 of the 19 targeted SNPs were significantly associated with overall susceptibility for CD. Associations with one additional SNP was borderline non-significant. Significantly associated SNPs included SNPs rs1250550 (p = 0.026) and rs8049439 (p = 0.04), recently reported to be specifically associated with pediatric-onset CD.Based on the results, we confirmed associations between two of the three novel pediatric-CD loci and other regions reported for associations with either pediatric and/or adult-onset CD.     

Localization in the gasserian ganglion of axons innervating the common hairs of the mystacial pad in the normal adult rat and in rats dewhiskered at birth

The neurons which innervate the small common hairs of the mystacial pad are shown to be located in the dorsomedial part of the ganglion of Gasser. In ganglia atrophied as a consequence of early destruction of vibrissae follicles, neurons that innervate these small hairs are still active.     

Genetic effect of mottled locus on reproduction and preweaning growth in laboratory mice

Summary An experiment was conducted to study the maternal and fetal effects of the sex-linked gene tortoise on litter size, birth weight, body weight from birth to 30-day of age, and mortality in normal (N) and mutant (M) mice (Mus musculus). The experiment involved two mating types: (1) N x N (dam x sire) which produced normal male and normal female offspring and (2) M X N which produced mutant males that died in utero, mutant females and normal male and female offspring. Comparison 1 consisted of all phenotypically normal male and female offspring from both N X N and M X N mating types born in 2 parities. The data supports the hypothesis that the tortoise gene, when present in the dam, did not significantly affect the body weight of normal progeny prior to 18 days old. There is also evidence for a negative maternal effect of the tortoise gene on body weight from 21 to 30 days of age postpartum. Mating type X parity interaction was not significant prior to 9 day postpartum. Sex of mice did not influence body weight of siblings prior to 18 day old, but males were heavier than females there-after. Normal and mutant females born in six parities from the M X N mating type constituted Comparison 2. The birth weight of the offspring in Comparison 2 was not significantly influenced by the presence of the tortoise gene. All other body weight measurements, however, were lower for mutant females when compared to normal females. Parity affected all body weight measurements in both comparisons. Mortality rate of the offspring was not influenced by parental mating type or parity, but sex differences were observed. Mutant females had higher mortality than normal sisters. This study provides evidence that the mottled locus in the tortoise dam and progeny influences growth and survival.Reference to a company and/or product named by the USDA is only for purposes of information and does not imply approval or recommendation of the product to the exclusion of others