Adaptive Phenotypic Differences to Low Potassium Soil of Two Cotton Genotypes with Various Potassium-Use Efficiencies

2012 ◽  
Vol 43 (15) ◽  
pp. 1984-1993
Author(s):  
Yong Tao ◽  
Li Wang ◽  
Xiao Wang ◽  
Ying Xia ◽  
Kaiyuan Wan ◽  
...  
2019 ◽  
Vol 1 (4) ◽  
pp. 23-27
Author(s):  
Saidzhamol T. Saidov ◽  
Viktor A. Dragavtsev ◽  
Asliddin T. Sadikov

This article presents the results of determining the attracting ability of the whole box and the degree of its differences depending on the genotypes, as well as its prospects for solving practical problems of selection of medium-fiber cotton. Consequently, among the genotypes studied by us, a significant amount of the attractive ability of a single box, the value of attraction and the mass of raw cotton per box differed in 10 combinations, which are economically the most productive.


2019 ◽  
Vol 1 (3) ◽  
pp. 17-20
Author(s):  
Asliddin T. Sadikov

Some economically valuable traits of upland cotton genotypes are being considered in comparison with standard cultivar “Hisor”. Based on the results, it was established that the yield of raw cotton for all studied genotypes is 66.4-100.1 g/plant. In a comparative analysis of highly productive genotypes, 3 genotypes were distinguished – ALC-86/6 x Sorbon, DP-4025 x Dusti-IZ, NAD-53 x Sorbon, varying from 95.0 to 100.1 g/plant, exceeding the standard cultivar “Hisor” (40,8 g/plant) by 54,2-59,3 g/plant.


Crop Science ◽  
1975 ◽  
Vol 15 (6) ◽  
pp. 782-784 ◽  
Author(s):  
Joseph O. Moffett ◽  
Lee S. Stith ◽  
Chris C. Burkhardt ◽  
Charles W. Shipman
Keyword(s):  

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Jaewon Lim ◽  
Hong-Tae Park ◽  
Seyoung Ko ◽  
Hyun-Eui Park ◽  
Gyumin Lee ◽  
...  

AbstractMycobacterium avium subsp. paratuberculosis (MAP) is a causative agent of Johne’s disease, which is a chronic granulomatous enteropathy in ruminants. Determining the genetic diversity of MAP is necessary to understand the epidemiology and biology of MAP, as well as establishing disease control strategies. In the present study, whole genome-based alignment and comparative analysis were performed using 40 publicly available MAP genomes, including newly sequenced Korean isolates. First, whole genome-based alignment was employed to identify new genomic structures in MAP genomes. Second, the genomic diversity of the MAP population was described by pangenome analysis. A phylogenetic tree based on the core genome and pangenome showed that the MAP was differentiated into two major types (C- and S-type), which was in keeping with the findings of previous studies. However, B-type strains were discriminated from C-type strains. Finally, functional analysis of the pangenome was performed using three virulence factor databases (i.e., PATRIC, VFDB, and Victors) to predict the phenotypic diversity of MAP in terms of pathogenicity. Based on the results of the pangenome analysis, we developed a real-time PCR technique to distinguish among S-, B- and C-type strains. In conclusion, the results of our study suggest that the phenotypic differences between MAP strains can be explained by their genetic polymorphisms. These results may help to elucidate the diversity of MAP, extending from genomic features to phenotypic traits.


Genetics ◽  
1996 ◽  
Vol 144 (2) ◽  
pp. 587-595 ◽  
Author(s):  
Mario de Bono ◽  
Jonathan Hodgkin

Abstract The tra-1 gene is a terminal regulator of somatic sex in Caenorhabditis elegans: high tra-1 activity elicits female development, low tra-1 activity elicits male development. To investigate the function and evolution of tra-1, we examined the tra-1 gene from the closely related nematode C. briggsae. Ce-tra-1 and Cb-tra-1 are unusually divergent. Each gene generates two transcripts, but only one of these is present in both species. This common transcript encodes TRA-1A, which shows only 44% amino acid identity between the species, a figure much lower than that for previously compared genes. A Cb-tra-1 transgene rescues many tissues of tra-1(nul1) mutants of C. elegans but not the somatic gonad or germ line. This transgene also causes nongonadal feminization of XO animals, indicating incorrect sexual regulation. Alignment of Ce-TRA-1A and Cb-TRA-1A defines several conserved regions likely to be important for tra-1 function. The phenotypic differences between Ce-tra-1(null) mutants rescued by Cb-tra-1 transgenes and wild-type C. elegans indicate significant divergence of regulatory regions. These molecular and functional studies suggest that evolution of sex determination in nematodes is rapid and genetically complex.


Author(s):  
Annelie Angerfors ◽  
Martina Olsson Lindvall ◽  
Björn Andersson ◽  
Staffan Nilsson ◽  
Marcela Davila Lopez ◽  
...  

AbstractDNA methylation has become increasingly recognized in the etiology of complex diseases, including thrombotic disorders. Blood is often collected in epidemiological studies for genotyping and has recently also been used to examine DNA methylation in epigenome-wide association studies. DNA methylation patterns are often tissue-specific, thus, peripheral blood may not accurately reflect the methylation pattern in the tissue of relevance. Here, we collected paired liver and blood samples concurrently from 27 individuals undergoing liver surgery. We performed targeted bisulfite sequencing for a set of 35 hemostatic genes primarily expressed in liver to analyze DNA methylation levels of >10,000 cytosine-phosphate-guanine (CpG) dinucleotides. We evaluated whether DNA methylation in blood could serve as a proxy for DNA methylation in liver at individual CpGs. Approximately 30% of CpGs were nonvariable and were predominantly hypo- (<25%) or hypermethylated (>70%) in both tissues. While blood can serve as a proxy for liver at these CpGs, the low variability renders these unlikely to explain phenotypic differences. We therefore focused on CpG sites with variable methylation levels in liver. The level of blood–liver tissue correlation varied widely across these variable CpGs; moderate correlations (0.5 ≤ r < 0.75) were detected for 6% and strong correlations (r ≥ 0.75) for a further 4%. Our findings indicate that it is essential to study the concordance of DNA methylation between blood and liver at individual CpGs. This paired blood–liver dataset is intended as a resource to aid interpretation of blood-based DNA methylation results.


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