Search bioRxiv⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/520338

Genetic Variability and Correlation Coefficients of Major Traits in Early Maturing Rice under Rainfed Lowland Environments of Nepal

Tiwari, D. N.·Tripathi, S. R.·Tripathi, M. P.·Khatri, N.·Bastola, B. R.
View original source ↗Export metadata ↓

Abstract

Genetic variability is the fundamental requirement of any crop breeding program to develop superior cultivars. The objective of this study was to estimate the genetic variability and find out the correlation among the different quantitative traits of rainfed early lowland rice. The experiment was conducted consecutively two years during 2015 and 2016 in wet season across the four different locations in Regional Agricultural Research Station, Khajura, National Wheat Research Program, Bhairahawa, National Maize Research Program, Rampur and National Rice Research Program, Hardinath along the Terai region of Nepal representing sub-tropical agro-climate. Seven genotypes including Hardinath-1 as standard check variety were evaluated in the randomized complete block design with three replications. Various quantitative traits were measured to investigate the variability and correlation coefficients. All the genotypes and locations showed significant variations for all the traits considered. Genotypic coefficient of variation was lower than phenotypic coefficient of variation for all traits studied. The magnitudes of genotypic coefficient of variations were relatively higher for grain yield, 1000-grain weight and days to heading. The highest broad sense heritability of 94% was recorded in days to maturity and the lowest heritability of 16% was observed in plant height. Positive and highly significant correlations were found both in genotypic and phenotypic levels between days to heading and days to maturity (rg=0.9999**, rp=0.997**), days to heading and grain yield (rg =0.9999**, rp= 0.9276**), days to maturity and grain yield (rg =0.9796**, rp=0.9174**). However, negative and highly significant genetic correlation was observed between plant height and 1000 grain weight (rg = -0.9999**). Thus results indicated that days to heading, days to maturity, grain yield, 1000 grain weight demonstrated higher heritability and remarkable genetic advance could be considered for the most appropriate traits for improvement and selection of trait to achieve stable and high yielding early rice genotypes under rainfed environments.

Source connections

Explore related subjects

geneticsPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Tiwari, D. N., Tripathi, S. R., Tripathi, M. P., Khatri, N., Bastola, B. R.. 2019-01-15. Genetic Variability and Correlation Coefficients of Major Traits in Early Maturing Rice under Rainfed Lowland Environments of Nepal. https://doi.org/10.1101/520338

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

OPA1 controls mitochondrial dysfunction-driven liver fibrosis in MASLD

Progressive hepatic fibrosis is the principal determinant of morbidity and mortality in metabolic dysfunction-associated steatotic liver disease and steatohepatitis (MASLD/MASH). Mitochondrial dysfunction is a hallmark of MASH, and the release of mitochondrial damage-associated molecular patterns (mito-DAMPs) from injured hepatocytes can promote fibrosis. However, how mitochondrial dynamics and quality control shape the fibrotic response in MASLD/MASH remains unclear. Here, through large-scale genomic analyses of mitochondrial genes governing mitophagy, fusion and fission in human MASLD, with a power-equivalent sample size of approximately 700,000 individuals, we identify a strong association between hepatic fibrosis and the mitochondrial fusion factor dynamin-like GTPase optic atrophy 1 (OPA1). OPA1 transcripts and protein abundance in the liver epithelium were progressively dysregulated with advancing fibrosis. In mice, hepatocyte-specific OPA1 loss alone was sufficient to induce hepatic stellate cell activation and fibrosis in zone 3, promoted the release of mito-DAMPs into the circulation and exacerbated fibrosis in experimental MASH. These findings identify OPA1 as a central regulator of the hepatic fibrotic response and connect defective mitochondrial homeostasis to mito-DAMP release, hepatic stellate cell activation and fibrosis in MASLD.

genetics↗
bioRxiv2026

Mechanism-selective deep mutational scanning distinguishes ERCC2 disease phenotypes

Pathogenic ERCC2 variants cause xeroderma pigmentosum (XP), trichothiodystrophy (TTD) or both, yet variant effect scores are usually interpreted only as measures of pathogenicity rather than of which disease mechanism is disrupted. XPD, the ERCC2-encoded TFIIH subunit, functions in both nucleotide excision repair and transcription. Using yeast complementation deep mutational scanning, we measured the effects of nearly all XPD amino acid substitutions. The assay was mechanism-selective: it preferentially reported transcription-associated function, with pronounced intolerance at the p44 interface, whereas many substitutions affecting DNA binding and helicase activity retained near-wild-type fitness. Accordingly, TTD variants had much lower fitness than XP variants. Computational predictors discriminated pathogenic from benign variants similarly across phenotypes, but the DMS distinguished XP from TTD variants better than all 73 predictors tested. Phenotype-specific ACMG/AMP calibration provided evidence in both directions for TTD but mainly pathogenic evidence for XP. Thus, the selectivity of functional assays, often viewed as a limitation, can reveal disease mechanisms and support phenotype-aware variant interpretation.

genetics↗
bioRxiv2026

Temporal control of mitochondrial mutagenesis reveals the fate of mtDNA mutations with age

Mutations in the mitochondrial genome (mtDNA) play a critical role in the aging process and a wide variety of age-related diseases. However, it remains unclear when the mutations that drive physiological decline arise. To answer this question, we generated a new mouse model in which mitochondrial mutagenesis can be confined to a defined window of time. Surprisingly, we found that mutations that arise during the first two months of life are sufficient to drive a wide variety of age-related pathologies, and that the severity of this pathology is broadly regulated by distinct, tissue-specific selective pressures that control the fate of mtDNA mutations with age. Further, we found that selection against deleterious variants can be modulated by manipulation of mitochondrial fusion in vitro and in vivo. These observations raise the possibility that in some tissues, the pace of aging is pre-determined by events that occur early in life and that interventions targeting mitochondrial fusion may be able to slow down or reverse the expansion of these pathogenic variants. These results carry far-reaching implications for strategies aimed at preventing or delaying age-related decline.

genetics↗