A comparative study of the mating call of Pelophylax ridibundus and Pelophylax kurtmuelleri (Anura: Ranidae) from syntopic and allotopic populations

The mating call of Pelophylax ridibundus and Pelophylax kurtmuelleri from three syntopic and five allotopic populations was studied. All recordings were made during the mating season. We tested the hypothesis that the call of P. ridibundus from allotopic populations would differ from that in syntopic populations with P. kurtmuelleri. For the comparative analysis we used univariate and multivariate statistical methods and the following characteristics: call duration, pulse group duration, pulse group interval, pulse group period, pulse group number, minimum, maximum, fundamental and dominant frequencies and pulse energy. Analyses reveal a trait divergence in most of the studied characteristics of the signals, with stronger differentiation between P. kurtmuelleri and P. ridibundus in syntopic populations than between the two species in allotopic ones. The possible evolutionary implications of this divergence are discussed.     

Forecasting private consumption: survey‐based indicators vs. Google trends

In this study we introduce a new indicator for private consumption based on search query time series provided by Google Trends. The indicator is based on factors extracted from consumption‐related search categories of the Google Trends application Insights for Search. The forecasting performance of the new indicator is assessed relative to the two most common survey‐based indicators: the University of Michigan Consumer Sentiment Index and the Conference Board Consumer Confidence Index. The results show that in almost all conducted in‐sample and out‐of‐sample forecasting experiments the Google indicator outperforms the survey‐based indicators. This suggests that incorporating information from Google Trends may offer significant benefits to forecasters of private consumption. Copyright © 2011 John Wiley & Sons, Ltd.     

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34

Congenital generalized lipodystrophy is an autosomal recessive disorder characterized by marked paucity of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes. We report several different mutations of the gene (AGPAT2) encoding 1-acylglycerol-3-phosphate O-acyltransferase 2 in 20 affected individuals from 11 pedigrees of diverse ethnicities showing linkage to chromosome 9q34. The AGPAT2 enzyme catalyzes the acylation of lysophosphatidic acid to form phosphatidic acid, a key intermediate in the biosynthesis of triacylglycerol and glycerophospholipids. AGPAT2 mRNA is highly expressed in adipose tissue. We conclude that mutations in AGPAT2 may cause congenital generalized lipodystrophy by inhibiting triacylglycerol synthesis and storage in adipocytes.     

Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking

Cranio-lenticulo-sutural dysplasia (CLSD) is an autosomal recessive syndrome characterized by late-closing fontanels, sutural cataracts, facial dysmorphisms and skeletal defects mapped to chromosome 14q13-q21 (ref. 1). Here we show, using a positional cloning approach, that an F382L amino acid substitution in SEC23A segregates with this syndrome. SEC23A is an essential component of the COPII-coated vesicles that transport secretory proteins from the endoplasmic reticulum to the Golgi complex. Electron microscopy and immunofluorescence show that there is gross dilatation of the endoplasmic reticulum in fibroblasts from individuals affected with CLSD. These cells also exhibit cytoplasmic mislocalization of SEC31. Cell-free vesicle budding assays show that the F382L substitution results in loss of SEC23A function. A phenotype reminiscent of CLSD is observed in zebrafish embryos injected with sec23a-blocking morpholinos. Our observations suggest that disrupted endoplasmic reticulum export of the secretory proteins required for normal morphogenesis accounts for CLSD.