The European stag beetle, Lucanus cervus, is recognised as a flagship species for biodiversity conservation. Although the species is widely distributed across Europe declines have led to it being granted protected or endangered status in a number of countries and regarded as "near threatened" by the IUCN. The integration of genetic approaches into conservation efforts is urgently needed but has been impeded to date by the lack of appropriate genetic markers. To provide such a resource the development of the first microsatellite loci for stag beetle is described. Loci were identified using two methods (i) enriched library cloning (ELC) and (ii) Restriction enzyme Associated DNA sequencing (RAD-Seq). Inefficient microsatellite detection using the ELC method suggests that RAD-Seq, or other Next Generation Sequencing based methods, may ultimately be more cost effective for obtaining informative suites of markers for this and other coleopteran species. 18 loci were characterised by genotyping 42 UK specimens collected as prey leftover/roadkill. All loci produced unambiguous genotypes and were polymorphic. Though preliminary, estimates of genetic variability suggest UK populations may be genetically depauperate. The microsatellite loci represent a suite of genetic markers that can be applied to non-invasive population monitoring and numerous other areas of Lucanus conservation and evolutionary research., Niall J. McKeown, Deborah J. Harvey, Amy J. E. Healey, Ilze Skujina, Karen Cox, Alan C. Gange, Paul W. Shaw., and Obsahuje bibliografii
Článek se zabývá taxonomií, reprodukční biologií, fylogenetikou, fylogeografií a introdukční historií ryb rodu karas (Carassius). Článek poskytuje souhrn poznatků, které jsou značně komplikované a spojené s jedinečným způsobem rozmnožování, definicí druhu a nepřesným chápáním biologie a systematiky těchto ryb v minulosti. Celá problematika je ještě daleko od svého kompletního vyřešení, ale současný pohled nám může pomoci v lepší péči o vodní prostředí., This article deals with the taxonomy, reproductive biology, phylogenetics, phylogeography and introduction history of the fishes of the genus Carassius. It summarizes findings associated with their unique mode of reproduction, challenging species delimitation and insufficient understanding of the biology and systematics of these fishes in the past. Deeper insight into the biology of Prussian Carp (Carassius gibelio) will require more research, but the available results can improve our understanding and management of the aquatic environment., Lukáš Kalous., and Obsahuje seznam literatury
Následující řádky přinášejí informaci o významném buněčném mechanismu, který pomáhá udržovat energetickou rovnováhu buněk v okamžicích náhlého zvýšení požadavku na dodávku energie. Tento mechanismus také usnadňuje přenos energeticky bohatých substrátů v buněčném prostoru k místům jeho spotřeby a je zvláště rozvinutý v buňkách, jejichž požadavky na dodávku energie v průběhu času značně kolísají a jsou schopné vysokého výkonu. Můžeme jej pozorovat ve svalových vláknech, srdečních myocytech, neuronech, ale i ve spermatických buňkách, které se po probuzení k aktivitě pokouší vyhrát závod s ostatními a splnit tím svoji biologickou úlohu., The article presents information on an important cell mechanism that helps to maintain the energy balance in cells at moments when there is a sudden increase in demand for energy supply. This mechanism also facilitates the transfer of energy-rich substrata in cellular space to the locations of its consumption, and it is particularly well-developed in cells that are capable of high performance and their energy requirements vary considerably over time. We can observe it in muscle fibres, cardiac myocytes, neurons and sperm cells., and Jitka Žurmanová.
The apolipoprotein A-V (apo A-V) plays an important role in regulation of triglyceride (TG) concentration in serum. To better understand how apo A-V affects triglyceridemia and glucoregulation, the lipoprotein lipase (LPL) activity was determined using intravenous fat tolerance test (IVFTT) and oral glucose tolerance test (oGTT) was performed in carriers of apolipoprotein A-V gene ( APOAV) variants known to be associated with increased triglyceridemia. Twelve carriers of 19W variant, 16 carriers of -1131C variant, 1 combined heterozygote and 16 control subjects homozygous for wild type variants (19S/-1131T) were selected from a population sample and matched with respect to body mass index and age. The APOAV variants carriers had increased TG, very low density lipoprotein-TG, and apo B concentrations (p < 0.05). The LPL activity evaluated as k2 rate constant for clearance of Intralipid® was 14 % lower in APOAV variants carriers. The depression of nonesterified fatty acids (NEFA) concentration after glucose load was delayed in APOAV variants carriers in spite of the same insulinemia and glycemia. Our results suggest that variants of APOAV combined with increased triglyceridemia are associated with lower LPL activity in vivo and with disturbances of regulation of NEFA concentration after glucose load., J. Kovář, V. Adámková., and Obsahuje bibliografii a bibliografické odkazy
The European Molecular Biology Organization organized a meeting in Prague October 1-3. At this symposium several topics were discussed: biology and genetics of mitochondria in relation to cancer; the role of mitochondria-targeting compounds in cancer suppression (including BH3 mimetics); mitochondria as transmitters of death receptor-induced apoptosis; regulation of apoptosis and the interplay of mitochondria with other organelles p53 and mitochondria in apoptosis regulation; and the role of mitochondria in targeting cancer stem cells. and Jiří Neužil, Ladislav Anděra a Alois Kozubík.
Patch clamp method developed more than 30 years ago is widely used for investigation of cellular excitability manifested as transmembrane ionic current and/or generation of action potentials. This technique could be applied to measurement of ionic currents flowing through individual (single) ion channels or through the whole assembly of ion channels expressed in the whole cell. Whole cell configuration is more common for measurement of ion currents and the only one enabling measurement of action potentials. This method allows detailed analysis of mechanisms and structural determinants of voltagedependent gating of ion channels as well as regulation of channel activity by intracellular signaling pathways and pharmacological agents., M. Karmažínová, L'. Lacinová., and Obsahuje bibliografii a bibliografické odkazy
The long QT syndrome (LQTS) is a monogenic disorder characterized by prolongation of the QT interval on electrocardiogram and syncope or sudden death caused by polymorphic ventricular tachycardia (torsades de pointes). In general, mutations in cardiac ion channel genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2) have been identified as a cause for LQTS. About 50-60 % of LQTS patients have an identifiable LQTS causing mutation in one of mentioned genes. In a group of 12 LQTS patients with no identified mutations in these genes we have tested a hypothesis that other candidate genes could be involved in LQTS pathophysiology. SCN1B and KCND3 genes encode ion channel proteins, ANK2 gene encodes cytoskeletal protein interacting with ion channels. To screen coding regions of genes SCN1B, KCND3, and 10 exons of ANK2 following methods were used: PCR, SSCP, and DNA sequencing. Five polymorphisms were found in screened candid ate genes, 2 polymorphisms in KCND3 and 3 in SCN1B. None of found polymorphisms has coding effect nor is located close to splice sites or has any similarity to known splicing enhancer motifs. Polymorphism G246T in SCN1B is a novel one. No mutation directly causing LQTS was found. Molecular mechanism of LQTS genesis in these patients remains unclear., M. Raudenská, A. Bittnerová, T. Novotný, A. Floriánová, K. Chroust, R. Gaillyová, B. Semrád, J. Kadlecová, M. Šišáková, O. Toman, J. Špinar., and Obsahuje bibliografii a bibliografické odkazy
Moravské zemské muzeum v Brně bylo vždy nositelem Mendelova badatelského odkazu, a to prostřednictvím bývalé vědecké akademie pro Moravu a Slezsko, tzv. Hospodářské společnosti (Ackerbaugesellschaft) a jejího Přírodozpytného spolku (Naturforschender Verein). Jako druhou největší a nejstarší muzejní instituci jej založila Moravskoslezská hospodářská společnost, jejímž členem se roku 1854 stal i Gregor Johann Mendel (1822-1884). Zapojil se nejen do organizační práce ve většině sekcí společnosti, ale také do výzkumu. Byl tedy v přímém kontaktu s počátečním vývojem současného Moravského zemského muzea. and Jiří Sekerák, Eva Matalová, Michal V. Šimůnek.
Disorders of ATP synthase, the key enzyme of mitochondrial energy provision belong to the most severe metabolic diseases presenting as early- onset mitochondrial encephalo- cardiomyopathies. Up to now, mutations in four nuclear genes were associated with isolated deficiency of ATP synthase. Two of them, ATP5A1 and ATP5E encode enzyme’s st ructural subunits α and ε , respectively, while the other two ATPAF2 and TMEM70 encode specific ancillary factors that facilitate the biogenesis of ATP synthase. All these defects share a similar biochemical phenotype with pronounced decrease in the content of fully assembled and functional ATP synthase complex. However, substantial differences can be found in their frequency, molecular mechanism of pathogenesis, clinical manifestation as well as the course of the disease progression. While for TMEM70 the number of reported patients as well as spectrum of the mutations is steadily increasing, mutations in ATP5A1, ATP5E and ATPAF2 genes are very rare. Apparently, TMEM70 gene is highly prone to mutagenesis and this type of a rare mitochondrial disease has a rather frequent incidence. Here we present overview of individual reported cases of nuclear mutations in ATP synthase and discuss, how their analysis can improve our understanding of the enzyme biogenesis., K. Hejzlarová ... [et al.]., and Obsahuje bibliografii a bibliografické odkazy