Effect of drought on yield components of maize hybrids : Zea mays L

When investigating drought tolerance, it must not be forgotten that drought stress is a complex phenomenon exhibiting quite different characters in different years and locations. For this reason, the plant response to drought is also a complex process. In our study, 83 maize hybrids originating from various countries were investigated over a period of two years, under irrigated and non-irrigated conditions. The drought tolerance of plants in the non-irrigated plots was analysed in terms of flowering synchrony and yield components. It could be concluded from the results that in response to long-term water deficit the period between tasselling and silking became longer, while the analysis of yield components revealed the greatest reductions in the number of kernels per ear and in the proportion of seed set. As the degree of proterandry increased, there was a decline in the grain yield, confirming that the analysis of this trait could be a way of predicting drought tolerance. Considerable differences in drought tolerance were observed between the genetic materials included in the analysis, suggesting the presence among these parental lines and hybrids of genotypes resistant to long-term water deficit, suitable for cultivation under dry conditions. An analysis of correlations between the traits revealed that proterandry should be treated as a priority trait when investigating drought stress tolerance, as better predictions can be made of both drought tolerance and potential yields, leading to more reliable selection for higher yields

Effect of drought on yield components of maize hybrids (Zea mays L)

When investigating drought tolerance, it must not be forgotten that drought stress is a complex phenomenon ex¬hibiting quite different characters in different years and locations. For this reason, the plant response to drought is also a complex process. In our study, 83 maize hybrids originating from various countries were investigated over a period of two years, under irrigated and non-irrigated conditions. The drought tolerance of plants in the non-irrigated plots was analysed in terms of flowering synchrony and yield components. It could be concluded from the results that in response to long-term water deficit the period between tasselling and silking became longer, while the analysis of yield components revealed the greatest reductions in the number of kernels per ear and in the proportion of seed set. As the degree of proterandry increased, there was a decline in the grain yield, confirming that the analysis of this trait could be a way of predicting drought tolerance. Considerable differences in drought tolerance were observed between the genetic materials included in the analysis, suggesting the presence among these parental lines and hybrids of genotypes resistant to long-term water deficit, suitable for cultivation under dry conditions. An analysis of correlations between the traits revealed that proterandry should be treated as a priority trait when investigating drought stress tolerance, as better predictions can be made of both drought tolerance and potential yields, leading to more reliable selection for higher yields

C70 Dimers – Energetics and Topology

All sp2 peanut-shaped dimeric fullerenes derived from D5h C70 are modeled. Construction of the isomers was monitored by a cyclic permutation of bonds in the linking zone of the two caps resulting from deleting the boundary of a face from the parent C70 fullerene. Local curvature was calculated in terms of both angular defects and strain energy. Topological equivalence classes of the constituent substructures were evaluated by calculating the topological indices of the parent cages, their medials and duals. Detailed network transformation, starting from C70, through sp3 dimer, peanut sp2 dimer, up to the corresponding tubulene is given. Semiempirical calculations showed a monotonic decrease in the heat of formation along the above pathway

Significance of the Tks4 scaffold protein in bone tissue homeostasis

Abstract The main driver of osteoporosis is an imbalance between bone resorption and formation. The pathogenesis of osteoporosis has also been connected to genetic alterations in key osteogenic factors and dysfunction of bone marrow mesenchymal stem/stromal cells (BM-MSCs). Tks4 (encoded by the Sh3pxd2b gene) is a scaffold protein involved in podosome organization. Homozygous mutational inactivation of Sh3pxd2b causes Frank-ter Haar syndrome (FTHS), a genetic disease that affects bone tissue as well as eye, ear, and heart functions. To date, the role of Tks4 in adult bone homeostasis has not been investigated. Therefore, the aim of this study was to analyze the facial and femoral bone phenotypes of Sh3pxd2b knock-out (KO) mice using micro-CT methods. In addition to the analysis of the Sh3pxd2b-KO mice, the bone microstructure of an FTHS patient was also examined. Macro-examination of skulls from Tks4-deficient mice revealed craniofacial malformations that were very similar to symptoms of the FTHS patient. The femurs of the Sh3pxd2b-KO mice had alterations in the trabecular system and showed signs of osteoporosis, and, similarly, the FTHS patient also showed increased trabecular separation/porosity. The expression levels of the Runx2 and osteocalcin bone formation markers were reduced in the bone and bone marrow of the Sh3pxd2b-KO femurs, respectively. Our recent study demonstrated that Sh3pxd2b-KO BM-MSCs have a reduced ability to differentiate into osteoblast lineage cells; therefore, we concluded that the Tks4 scaffold protein is important for osteoblast formation, and that it likely plays a role in bone cell homeostasis

Rare Copy Number Variants in \u3cem\u3eNRXN1\u3c/em\u3e and \u3cem\u3eCNTN6\u3c/em\u3e Increase Risk for Tourette Syndrome

Tourette syndrome (TS) is a model neuropsychiatric disorder thought to arise from abnormal development and/or maintenance of cortico-striato-thalamo-cortical circuits. TS is highly heritable, but its underlying genetic causes are still elusive, and no genome-wide significant loci have been discovered to date. We analyzed a European ancestry sample of 2,434 TS cases and 4,093 ancestry-matched controls for rare (\u3c 1% frequency) copy-number variants (CNVs) using SNP microarray data. We observed an enrichment of global CNV burden that was prominent for large (\u3e 1 Mb), singleton events (OR = 2.28, 95% CI [1.39–3.79], p = 1.2 × 10−3) and known, pathogenic CNVs (OR = 3.03 [1.85–5.07], p = 1.5 × 10−5). We also identified two individual, genome-wide significant loci, each conferring a substantial increase in TS risk (NRXN1 deletions, OR = 20.3, 95% CI [2.6–156.2]; CNTN6 duplications, OR = 10.1, 95% CI [2.3–45.4]). Approximately 1% of TS cases carry one of these CNVs, indicating that rare structural variation contributes significantly to the genetic architecture of TS