Flowering, germination and rooting of cuttings of Lippia L. (Verbenaceae)

Lippia species from Cadeia do Espinhaço (MG, Brazil), were collected and established at the Botanical Experimental Station, Juiz de Fora, MG. The flowering of plants was evaluated in both natural and controlled conditions. Germination test was accomplished with seeds obtained from natural conditions. The rooting of cuttings was evaluated in plants cultivated in the Botanical Experimental Station. The majority of species blossomed either in the dry or in the rainy seasons. Only one species blooms in both seasons. At controlled conditions, the flowering period increased in species that flourish in the summer. Some species presented better germination with fresh collected seeds while others when the seeds were stored, evidencing both viability loss and seed dormancy. GA3 stimulates the germination in some species, while it inhibited or not influenced on others. Some species germinate better in the darkness, while others under white light. Some of them germinate in the light or in the darkness. Adventitious roots formation in cuttings of wild species was very low and did not vary in response to season variation and auxin concentration. On the other hand, rooting of cuttings of L. alba (Mill.) N.E. Br. varied in response both to season variation and to auxin types and concentration. This is the first report on physiological reproductive aspects of endemic Lippia species from the Cadeia do Espinhaço. The results indicate the possibility to use seeds in the propagation of wild Lippia species and, they also show that reproduction through conventional vegetative propagation techniques presents quite reduced efficiency.Plantas de dez espécies de Lippia foram coletadas na Cadeia do Espinhaço, MG, Brasil e cultivadas em canteiros em Juiz de Fora, MG. A época de florescimento das espécies de Lippia foi observada nos ambientes de origem e em canteiro. A germinação foi testada com sementes coletadas em ambiente natural. Os materiais estabelecidos ex situ foram avaliados quanto ao enraizamento de estacas. As análises das plantas em ambiente natural e das cultivadas em canteiro evidenciaram que a maioria das espécies estudadas apresenta floração no período seco (inverno), enquanto um menor número, no chuvoso (verão). Uma única espécie floresceu nessas duas estações. Em cultivo controlado, o período de floração das espécies com floração característica no verão foi aumentado. Algumas espécies germinaram melhor quando recém coletadas enquanto outras quando armazenadas, evidenciando a ocorrência de perda de viabilidade e de dormência. O GA3 estimulou a germinação em algumas espécies, enquanto inibiu ou não apresentou efeitos sobre outras. Sementes de algumas espécies germinaram melhor no escuro, enquanto de outras sob luz branca, existindo ainda espécies que germinaram tanto na luz quanto no escuro. O enraizamento das estacas das espécies não domesticadas de Lippia foi muito baixo, independente da estação do ano e da concentração da auxina. O enraizamento em estacas de L. alba (Mill.) N.E. Br. variou em resposta à época de coleta das estacas e quanto ao tipo e à concentração das auxinas utilizadas. Os resultados do presente trabalho constituem os primeiros relatos envolvendo a reprodução de espécies de Lippia endêmicas da Cadeia do Espinhaço. Eles indicam a possibilidade de utilização das sementes na propagação das plantas desse gênero e também evidenciam que a reprodução das plantas das espécies não domesticadas de Lippia através de técnicas convencionais de propagação assexuada apresenta eficiência bastante reduzida

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.

To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping projects totaling 25,509 EOC cases and 40,941 controls. We identified nine new susceptibility loci for different EOC histotypes: six for serous EOC histotypes (3q28, 4q32.3, 8q21.11, 10q24.33, 18q11.2 and 22q12.1), two for mucinous EOC (3q22.3 and 9q31.1) and one for endometrioid EOC (5q12.3). We then performed meta-analysis on the results for high-grade serous ovarian cancer with the results from analysis of 31,448 BRCA1 and BRCA2 mutation carriers, including 3,887 mutation carriers with EOC. This identified three additional susceptibility loci at 2q13, 8q24.1 and 12q24.31. Integrated analyses of genes and regulatory biofeatures at each locus predicted candidate susceptibility genes, including OBFC1, a new candidate susceptibility gene for low-grade and borderline serous EOC

The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor

Simple SummaryIt is well-recognised the strong contribution of genetic factors to prostate cancer (PrCa) susceptibility, thus genetic screening is critical for presymptomatic diagnosis and identification of individuals at high-risk. In this context, recurrent founder variants in cancer predisposing genes, by providing specific targets for early identification of carriers at risk of developing the disease, may be leveraged to implement cost-efficient targeted genetic screening strategies. The goal of this study was to investigate whether CHEK2 c.349A>G, the only recurrent "likely pathogenic" variant in CHEK2 gene reported in the Portuguese population, plays an important role in PrCa development, and the possibility of a founder effect behind its origin. Our results clearly demonstrate that c.349A>G in the CHEK2 tumour-suppressor gene is a founder variant significantly associated with an increased risk of PrCa, suggesting its potential usefulness for cost-effective targeted genetic screening in PrCa families.The identification of recurrent founder variants in cancer predisposing genes may have important implications for implementing cost-effective targeted genetic screening strategies. In this study, we evaluated the prevalence and relative risk of the CHEK2 recurrent variant c.349A>G in a series of 462 Portuguese patients with early-onset and/or familial/hereditary prostate cancer (PrCa), as well as in the large multicentre PRACTICAL case-control study comprising 55,162 prostate cancer cases and 36,147 controls. Additionally, we investigated the potential shared ancestry of the carriers by performing identity-by-descent, haplotype and age estimation analyses using high-density SNP data from 70 variant carriers belonging to 11 different populations included in the PRACTICAL consortium. The CHEK2 missense variant c.349A>G was found significantly associated with an increased risk for PrCa (OR 1.9; 95% CI: 1.1-3.2). A shared haplotype flanking the variant in all carriers was identified, strongly suggesting a common founder of European origin. Additionally, using two independent statistical algorithms, implemented by DMLE+2.3 and ESTIAGE, we were able to estimate the age of the variant between 2300 and 3125 years. By extending the haplotype analysis to 14 additional carrier families, a shared core haplotype was revealed among all carriers matching the conserved region previously identified in the high-density SNP analysis. These findings are consistent with CHEK2 c.349A>G being a founder variant associated with increased PrCa risk, suggesting its potential usefulness for cost-effective targeted genetic screening in PrCa families

Contributions of mean and shape of blood pressure distribution to worldwide trends and variations in raised blood pressure: A pooled analysis of 1018 population-based measurement studies with 88.6 million participants

© The Author(s) 2018. Background: Change in the prevalence of raised blood pressure could be due to both shifts in the entire distribution of blood pressure (representing the combined effects of public health interventions and secular trends) and changes in its high-blood-pressure tail (representing successful clinical interventions to control blood pressure in the hypertensive population). Our aim was to quantify the contributions of these two phenomena to the worldwide trends in the prevalence of raised blood pressure. Methods: We pooled 1018 population-based studies with blood pressure measurements on 88.6 million participants from 1985 to 2016. We first calculated mean systolic blood pressure (SBP), mean diastolic blood pressure (DBP) and prevalence of raised blood pressure by sex and 10-year age group from 20-29 years to 70-79 years in each study, taking into account complex survey design and survey sample weights, where relevant. We used a linear mixed effect model to quantify the association between (probittransformed) prevalence of raised blood pressure and age-group- and sex-specific mean blood pressure. We calculated the contributions of change in mean SBP and DBP, and of change in the prevalence-mean association, to the change in prevalence of raised blood pressure. Results: In 2005-16, at the same level of population mean SBP and DBP, men and women in South Asia and in Central Asia, the Middle East and North Africa would have the highest prevalence of raised blood pressure, and men and women in the highincome Asia Pacific and high-income Western regions would have the lowest. In most region-sex-age groups where the prevalence of raised blood pressure declined, one half or more of the decline was due to the decline in mean blood pressure. Where prevalence of raised blood pressure has increased, the change was entirely driven by increasing mean blood pressure, offset partly by the change in the prevalence-mean association. Conclusions: Change in mean blood pressure is the main driver of the worldwide change in the prevalence of raised blood pressure, but change in the high-blood-pressure tail of the distribution has also contributed to the change in prevalence, especially in older age groups