Semi-dwarf narrow rolled leaf mutant in rice: Photosynthetic efficiency and physiological response to gibberellic acid (GA3)

Leaf is the major component for fixation of carbondioxide to produce more photoassimilates and maintains source sink relationship in plants. The present investigation was carried out to study the photosynthetic efficiency and physiological response of GA3 of semi-dwraf narrow rolled leaf mutant. Semi-dwarf narrow rolled leaf mutant exhibited reduced plant height, reduced leaf width, reduced panicle length and number of grains per panicle when compared to wild type. Photosynthetic efficiency study revealed that the mutant showed higher photosynthetic efficiency than wild type. Complementation test with GA3 clearly revealed that this mutant is sensitive to GA3 and revert to normal plant height. Scanning Electron Microscope study revealed that mutant had exhibited minimum number of inter-veins between veins, minimum distance between midrib and has slightly larger cell size. Hence, this loss of function mutant is very useful to map the regions associated with panicle length, number of grains per panicle and other traits related to enhancement of yield. The result provides an important clue for further understanding the mechanism of rice leaf development and plant architecture

Fine mapping of rice drought QTL and study on combined effect of QTL for their physiological parameters under moisture stress condition

The present investigation was undertaken to study the effect of different yield QTL (DTY2.2, DTY3.1 and DTY8.1) under drought and their physiological response to drought stress. Backcross Inbred Lines (BILs) of IR64 (CB-193 and CB-229) along with IR64, APO and the traditional rice variety Norungan were raised in green house condition under water stress and control to evaluate the effect of the QTL on grain yield. The BIL CB-193 recorded higher photosynthetic rate (22.051), transpiration rate (7.152) and Ci/Ca ratio (0.597) whereas the BIL CB-229 recorded high relative water content (80.76%). It was found that the combination of three QTL (CB-229) performed better than the susceptible parent and the line with two QTL (CB-193 Fine-mapping of two QTLs viz., qDTY2.2 and qDTY8.1, for grain yield (GY) were conducted using backcross derived lines. Composite interval mapping analyses resolved the originally identified qDTY2.2 region of 6.7 cM into a segment of 2.1 cM and two sub QTLs at region between RM23132 and RM1578 (75.75 cM- 77.66 cM), RM515 and RM1578 (75.11 cM-77.66 cM) were identified in qDTY8.1 region. However this study provides a unique opportunity to breeders to introgress such regions together as a unit into high-yielding drought-susceptible varieties through MAS

Assessment of variability parameters and diversity of panicle architectural traits associated with yield in rice (Oryza sativa L.)

The rice panicle, a pivotal reproductive structure, signifies the transition from vegetative to reproductive growth in plants. Comprising components such as the rachis, primary and secondary branches, seed quantities and branch lengths, panicle architecture profoundly influences grain production. This study delves into the diversity of panicle architecture traits and scrutinizes variability parameters across 69 distinct rice genotypes. Our findings underscore substantial variations in panicle architecture traits among genotypes. Particularly noteworthy are traits with the highest coefficient of variation (CV%), encompassing the count of secondary branches, single plant yield, productive tillers per plant, seeds per secondary branch and panicle weight. Correlation analysis reveals robust positive connections between panicle weight, the number of filled grains per panicle, 1000-grain weight and single plant yield. The number of secondary branches exhibits the most substantial phenotypic coefficient of variation (PCV%) at 47.14%, accompanied by a genotypic coefficient of variation (GCV%) of 43.57%. Traits such as days to 50% flowering, plant height and number of filled grains per panicle manifest high heritability (97.04%, 91.24% and 76.22% respectively) and notable genetic advancement (23.11%, 39.62% and 47.49%). The principal component analysis identifies the primary component (PC1) as the principal contributor to variance. Biplot analysis accentuates positive correlations between attributes like the number of filled grains per panicle, panicle length, plant height, primary branch count, panicle weight, seeds per primary branch and the number of secondary branches with single plant yield. By employing Mahalanobis D2 statistics, the classification of genotypes into 6 distinct clusters reveals clusters III and IV as distinguished by their significant inter-cluster and intra-cluster distances. This comprehensive analysis unveils the potential for harnessing panicle architecture traits to enhance grain production and advances our comprehension of intricate relationships within diverse rice genotypes

Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss

Otosclerosis (OTSC) is a complex bone disorder of the otic capsule, which causes conductive hearing impairment in human adults. The dysregulation of the signaling axis mediated by the receptor activator of nuclear factor-kappa-B (RANK), RANK ligand (RANKL), and osteoprotegerin has been widely attributed to the context of metabolic bone disorders. While genetic associations and epigenetic alterations in the TNFSF11 gene (RANKL) have been well-linked to metabolic bone diseases of the skeleton, particularly osteoporosis, they have never been addressed in OTSC. This study aimed to assess whether the genetic association of rs1021188 polymorphism in the upstream of TNFSF11 and the DNA methylation changes in its promoter CpG-region reveal the susceptibility of OTSC. Peripheral blood DNA samples were collected from unrelated Tunisian-North African subjects for genotyping (109 cases and 120 controls) and for DNA methylation analysis (40 cases and 40 controls). The gender-stratified analysis showed that the TNFSF11 rs1021188 C/T was associated with OTSC in men (p = 0.023), but not in women (p = 0.458). Individuals with CC genotype were more susceptible to OTSC, suggesting an increased risk to disease development. Using publicly available data, the rs1021188 was within a cluster grouping the subpopulations with African ethnicity. Moreover, 26 loci in the TNFSF11 gene were in linkage disequilibrium with rs1021188, revealing relative similarities between different populations. Significant differences in both DNA methylation and unmethylation status were detected with 4.53- and 4.83-fold decreases in the global DNA methylation levels in female and male OTSC groups, respectively. These changes could contribute to an increased risk of OTSC development. Bioinformatic analyses indicated that each of the rs1021188 variations and the DNA methylation changes in the promoter CpG-sites within TNFSF11 may play an important role in its transcription regulation. To our knowledge, this is the first study that investigates an independent effect of the rs1021188 polymorphism and DNA hypomethylation of TNFSF11 promoter in OTSC. Genetic and epigenetic changes in the regulatory regions of TNFSF11 could offer new molecular insights into the understanding of the complexity of OTSC

The Proportion of Endometrial Tumours Associated with Lynch Syndrome (PETALS): a prospective cross-sectional study

This is the final version. Available on open access from the Public Library of Science via the DOI in this recordBackground: Lynch syndrome (LS) predisposes to endometrial (EC), colorectal and other cancers through inherited pathogenic variants affecting mismatch-repair (MMR) genes. Diagnosing LS in women with EC can reduce subsequent cancer mortality through colonoscopic surveillance and aspirin chemoprevention; it also enables cascade testing of relatives. A growing consensus supports LS screening in EC, however, the expected proportion of test-positives and optimal testing strategy is uncertain. Previous studies from insurance-based healthcare systems were limited by narrow selection criteria, failure to apply reference standard tests consistently and poor conversion to definitive testing. The aim of this study was to establish the prevalence of LS and the diagnostic accuracy of LS testing strategies in an unselected EC population. Methods and Findings: This was a prospective cross-sectional study carried out at a large UK gynaecological cancer centre between October/2015 and January/2017. Women diagnosed with EC or atypical hyperplasia (AH) were offered LS testing. Tumours underwent MMR immunohistochemistry (IHC), microsatellite instability (MSI) and targeted MLH1-methylation testing. Women <50 years, with strong family histories and/or indicative tumour molecular features underwent MMR germline sequencing. Somatic MMR sequencing was performed when indicative molecular features were unexplained by LS or MLH1-hypermethylation. The main outcome measures were the prevalence of LS in an unselected EC population and the diagnostic accuracy of clinical and tumour testing strategies for risk stratifying women with EC for MMR germline sequencing. In total, 500 women participated in the study; only 2 (<1%) declined. Germline sequencing was indicated and conducted for 136 and 135 women, respectively. 16/500 women (3.2%, 95% CI 1.8% to 5.1%) had LS and 11 more (2.2%) had MMR variants of uncertain significance. Restricting testing to age <50 years, indicative family history (revised Bethesda guidelines or Amsterdam-II criteria) or endometrioid histology alone would have missed 9 (56%), 11 (69%) or 12 (75%), and 5 (31%) of the 16 cases of LS, respectively. In total 132/500 tumours were MMR-deficient by IHC, of which 83/132 (63%) had MLH1-hypermethylation and 16/49 (33%) of the remaining patients had LS (16/132 with MMR-deficiency, 12%). MMR-IHC with targeted MLH1-methylation testing was more discriminatory for LS than MSI/methylation testing, with 100% versus 56.3% (16/16 versus 9/16) sensitivity (p=0.016) and equal 97.5% (468/484) specificity. 64% MSI-H and 73% MMR-deficient tumours unexplained by LS or MLH1-hypermethylation had somatic MMR-mutations. The main limitation of the study was failure to conduct MMR germline sequencing for the whole study population, which means that the sensitivity and specificity of tumour triage strategies for LS detection may be over-estimated, although the risk of LS in women with no clinical or tumour predictors is expected to be extremely low. Conclusions: In this study, we observed that age, family history and histology are imprecise clinical correlates of LS-EC. IHC outperformed MSI for tumour triage, and reliably identified both germline and somatic MMR mutations. The 3.2% proportion of LS-EC is similar to colorectal cancer, supporting unselected screening of EC for LS.

Corporate Social Responsibility Strategies of Spanish Listed Firms and Controlling Shareholders’ Representatives

This article aims at analyzing how controlling shareholders’ representatives on boards affect corporate social responsibility (CSR) strategies (disclosing CSR matters) in Spain, a context characterized by high ownership concentration, one-tier boards, little board independence, weak legal protection for investors, and the presence of large shareholders, especially institutional shareholders. Furthermore, among controlling shareholders’ representatives, we can distinguish between those appointed by insurance companies and banks and those appointed by mutual funds, investment funds, and pension funds. The effect of these categories of directors on CSR strategies is, therefore, also analyzed. Our findings suggest that controlling shareholders’ representatives have a positive effect on CSR strategies, as do directors appointed by investment funds, pension funds, and mutual funds, while directors appointed by banks and insurance companies have no impact on CSR strategies. This analysis offers new insights into the role played by certain types of directors on CSR strategies

Are market perceptions of corporate layoffs changing?

We examine the response of stock returns to corporate layoff announcements for the 12-year period from 1981 to 1992. The results indicate a dramatic shift in the investors' perception of initiatives to reduce the number of employees. While there were negative abnormal returns associated with the announcements during the recessionary and boom periods of the 1980s, there are positive abnormal returns associated with the announcements in the early 1990s. This evidence suggests that important structural changes in the U.S. labor market may be underway. © 1995.link_to_subscribed_fulltex

Stock prices, inflation and output: Evidence from India

A negative relationship between stock market returns and inflationary trends has been widely documented for developed economies in Europe and North America. This study provides similar evidence for India. The study investigates the relationship in light of Fama's (1981) explanation that centers around linkages between inflation and real activity, and between stock returns and real activity. The results provide only partial support for Fama's hypothesis. The relationship between real activity and inflation does not account for the negative relationship between real stock returns and the unexpected component of inflation. (JEL: F31, 053).link_to_subscribed_fulltex