18 research outputs found
A novel human pain insensitivity disorder caused by a point mutation in ZFHX2
Chronic pain is a major global public health issue causing a severe impact on both the quality
of life for sufferers and the wider economy. Despite the significant clinical burden, little
progress has been made in terms of therapeutic development. A uniquepowerful approach to
identifying new human-validated analgesic drug targets is to study rare families with
inherited pain insensitivity. Here we have analysed an otherwise normal family where six
affected individuals display a pain insensitive phenotype that is characterized by
hyposensitivity to noxious heat and painless bone fractures. This autosomal dominant
disorder is found in three generations and is not associated with a peripheral neuropathy. A
novel point mutation in ZFHX2, encoding a putative transcription factor expressed in small
diameter sensory neurons, was identified by whole exome sequencing that segregates with
the pain insensitivity. The mutation is predicted to change an evolutionarily highly conserved
arginine residue 1913 to a lysine within a homeodomain. BAC transgenic mice bearing the
orthologous murine p.R1907K mutation, as well as Zfhx2 null mutant mice, have significant
deficits in pain sensitivity. Gene expression analyses in dorsal root ganglia from mutant and
wild-type mice show altered expression of genes implicated in peripheral pain mechanisms.
The ZFHX2 variant and downstream regulated genes associated with a human paininsensitive
phenotype are therefore potential novel targets for the development of new
analgesic drugs
Leptin-mediated modulation of steroidogenic gene expression in hypoxic zebrafish embryos: Implications for the disruption of sex steroids
Hypoxia can impair reproduction of fishes through the disruption of sex steroids. Here, using zebrafish (Danio rerio) embryos, we investigated (i) whether hypoxia can directly affect steroidogenesis independent of pituitary regulation via modulation of steroidogenic gene expression, and (ii) the role of leptin in hypoxia-induced disruption of steroidogenesis. Exposure of fertilized zebrafish embryos to hypoxia (1.0 mg O 2 L -1) from 0-72 h postfertilization (hpf), a developmental window when steroidogenesis is unregulated by pituitary influence, resulted in the up-regulation of cyp11a, cyp17, and 3β-hsd and the down-regulation of cyp19a. Similar gene expression patterns were observed for embryos exposed to 10 mM cobalt chloride (CoCl 2, a chemical inducer of hypoxia-inducible factor 1, HIF-1), suggesting a regulatory role of HIF-1 in steroidogenesis. Testosterone (T) and estradiol (E2) concentrations in hypoxic embryos were greater and lesser, respectively, relative to the normoxic control, thus leading to an increased T/E2 ratio. Expression of the leptin-a gene (zlep-a) was up-regulated upon both hypoxia and CoCl 2 treatments. Functional assays suggested that under hypoxia, elevated zlep-a expression might activate cyp11a and 3β-hsd and inhibit cyp19a. Overall, this study indicates that hypoxia, possibly via HIF-1-induced leptin expression, modulates sex steroid synthesis by acting directly on steroidogenic gene expression. © 2012 American Chemical Society.link_to_subscribed_fulltex
Experimental and theoretical study of the low-temperature kinetics of the reaction of CN with CH2O and implications for interstellar environments
Rate coefficients for the reaction of CN with CH2O were measured for the first time below room temperature in the range 32 – 103 K using a pulsed Laval nozzle apparatus together with the Pulsed Laser Photolysis–Laser-Induced Fluorescence technique. The rate coefficients exhibited a strong negative temperature dependence, reaching (4.62±0.84) × 10 11 cm3molecule-1s-1 at 32 K, and no pressure dependence was observed at 70 K. The potential energy surface (PES) of the CN + CH2O reaction was calculated at the CCSD(T)/aug-cc-pVTZ//M06-2X/aug-cc-pVTZ level of theory, with the lowest energy channel to reaction characterized by the formation of a weakly-bound van der Waals complex, bound by 13.3 kJ mol-1, prior to two transition states with energies of 0.62 and 3.97 kJ mol 1, leading to the products HCN + HCO or HNC + HCO, respectively. For the formation of formyl cyanide, HCOCN, a large activation barrier of 32.9 kJ mol-1 was calculated. Reaction rate theory calculations were performed with the MESMER (Master Equation Solver for Multi Energy well Reactions) package on this PES to calculate rate coefficients. While this ab initio description provided good agreement with the low-temperature rate coefficients, it was not capable of describing the high-temperature experimental rate coefficients from the literature. However, increasing the energies and imaginary frequencies of both transition states allowed MESMER simulations of the rate coefficients to be in good agreement with data spanning 32 – 769 K. The mechanism for the reaction is formation of a weakly-bound complex followed by quantum mechanical tunnelling through the small barrier to form HCN + HCO products. MESMER calculations showed that channel generating HNC is not important. MESMER simulated the rate coefficients from 4 – 1000 K which were used to recommend best-fit modified Arrhenius expressions for use in astrochemical modelling. The UMIST Rate12 (UDfa) model yielded no significant changes in the abundances of HCN, HNC, and HCO for a variety of environments upon inclusion of rate coefficients reported here. The main implication from this study is that the title reaction is not a primary formation route to the interstellar molecule formyl cyanide, HCOCN, as currently implemented in the KIDA astrochemical model