Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma

Background  

DBA/2J (D2) mice develop an age-related form of glaucoma. Their eyes progressively develop iris pigment dispersion and iris atrophy followed by increased intraocular pressure (IOP) and glaucomatous optic nerve damage. Mutant alleles of the Gpnmb and Tyrp1 genes are necessary for the iris disease, but it is unknown whether alleles of other D2 gene(s) are necessary for the distinct later stages of disease. We initiated a study of congenic strains to further define the genetic requirements and disease mechanisms of the D2 glaucoma.     

Nucleotides and related compounds in bracken

The role of sugar nucleotides in polysaccharide synthesis is discussed. The presence of acid soluble nucleotides in bracken rhizomes was demonstrated (20 μmol/kg fresh weight) and the uridine series was shown to predominate accounting for some 80% of the total. The following were identified, UDP-glucose (60%), UDP-galactose (15%), UDP-xylose (9%), UDP-arabinose (3%), UDP-glucuronic acid (4%), GDP-mannose (6%) and GDP-fucose (3%). It is probable that these sugar nucleotides supply the full complement of sugars identified in the carbohydrate fractions of bracken.     

Ontogeny of intersexual head shape and prey selection in the pitviper Agkistrodon piscivorus

Different animal intraspecific classes commonly differ in their prey selection. Such differences in feeding ecology are thought to reduce resource competition between classes, but other factors (i.e. behavioural, morphological, and physiological differences) also contribute to this widespread phenomenon. Although several studies have correlated the size of the feeding apparatus with prey selection in many animals, few studies have examined how the shape of the feeding apparatus is related to prey selection. Furthermore, even though the dietary regimen of many animals changes during ontogeny, few studies have examined how shape changes in the feeding apparatus may be related to these ontogenetic dietary shifts. Here we address these issues by examining how head shape, head size and prey selection change over ontogeny in adult males, adult females and juveniles of the cottonmouth snake Agkistrodon piscivorus . Our scaling data for head characteristics showed that all head measurements in adult male and female A. piscivorus scaled with significant negative allometry, whereas juvenile head measurements typically scaled isometrically, except for head volume (positive) and head length (negative). Thus, juveniles have relatively broad and high, but short, heads. Large adult male and female A. piscivorus have relatively small head dimensions overall. Thus, juveniles appear to undergo a rapid change in head volume, which subsequently slows considerably as sexual maturity is achieved. However, our multivariate analysis of size-adjusted head dimensions showed that juveniles differed only slightly in their head shape compared with adult male and female A. piscivorus . In general, prey size increased with snake size across all age and sex groups, but an ontogenetic shift in prey type was not detected in either males or females.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 81 , 151–159.     

Oncogenic comparison of human papillomavirus type 58 E7 variants

Human papillomavirus 58 (HPV58) ranks the second or third in East Asian cervical cancers. Current studies on HPV58 are scarce and focus on the prototype. Previously, we identified the three most common circulating HPV58 E7 strains contained amino acid alterations: G41R/G63D (51%), T20I/G63S (22%) and T74A/D76E (14%) respectively. Among them, the T20I/G63S variant (V1) had a stronger epidemiological association with cervical cancer. We therefore suggested that V1 possessed stronger oncogenicity than the other two variants. Here, we performed phenotypic assays to characterize and compare their oncogenicities with HPV58 E7 prototype. Our results showed that overexpression of V1 conferred a higher colony‐forming ability to primary murine epithelial cells than prototype (P < 0.05) and other variants, implicating its higher immortalising potential. Further experiments showed that both V1 and prototype enhanced the anchorage‐independent growth of NIH/3T3 cells (P < 0.001), implicating their stronger transforming power than the two other variants. Moreover, they possessed an increased ability to degrade pRb (P < 0.001), which is a major effector pathway of E7‐driven oncogenesis. Our work represents the first study to compare the oncogenicities of HPV58 E7 prototype and variants. These findings deepened our understanding of HPV58 and might inform clinical screening and follow‐up strategy.