Expression of genes associated with carbohydrate metabolism in cotton stems and roots

<p>Abstract</p> <p>Background</p> <p>Cotton (<it>Gossypium hirsutum </it>L) is an important crop worldwide that provides fiber for the textile industry. Cotton is a perennial plant that stores starch in stems and roots to provide carbohydrates for growth in subsequent seasons. Domesticated cotton makes these reserves available to developing seeds which impacts seed yield. The goals of these analyses were to identify genes and physiological pathways that establish cotton stems and roots as physiological sinks and investigate the role these pathways play in cotton development during seed set.</p> <p>Results</p> <p>Analysis of field-grown cotton plants indicated that starch levels peaked about the time of first anthesis and then declined similar to reports in greenhouse-grown cotton plants. Starch accumulated along the length of the stem and the shape and size of the starch grains from stems were easily distinguished from transient starch. Microarray analyses compared gene expression in tissues containing low levels of starch with tissues rapidly accumulating starch. Statistical analysis of differentially expressed genes indicated increased expression among genes associated with starch synthesis, starch degradation, hexose metabolism, raffinose synthesis and trehalose synthesis. The anticipated changes in these sugars were largely confirmed by measuring soluble sugars in selected tissues.</p> <p>Conclusion</p> <p>In domesticated cotton starch stored prior to flowering was available to support seed production. Starch accumulation observed in young field-grown plants was not observed in greenhouse grown plants. A suite of genes associated with starch biosynthesis was identified. The pathway for starch utilization after flowering was associated with an increase in expression of a glucan water dikinase gene as has been implicated in utilization of transient starch. Changes in raffinose levels and levels of expression of genes controlling trehalose and raffinose biosynthesis were also observed in vegetative cotton tissues as plants age.</p

Insights into the evolution of the New World diploid cottons (Gossypium, subgenus Houzingenia) based on genome sequencing

We employed phylogenomic methods to study molecular evolutionary processes and phylogeny in the geographically widely dispersed New World diploid cottons (Gossypium, subg. Houzingenia). Whole genome resequencing data (average of 33X genomic coverage) were generated to reassess the phylogenetic history of the subgenus and provide a temporal framework for its diversification. Phylogenetic analyses indicate that the subgenus likely originated following trans-oceanic dispersal from Africa about 6.6 mya, but that nearly all of the biodiversity evolved following rapid diversification in the mid-Pleistocene (0.5-2.0 mya), with multiple long-distance dispersals required to account for range expansion to Arizona, the Galapagos Islands, and Peru. Comparative analyses of cpDNA vs. nuclear data indicate that this history was accompanied by several clear cases of interspecific introgression. Repetitive DNAs contribute roughly half of the total 880 Mb genome, but most transposable element families are relatively old and stable among species. In the genic fraction, pairwise synonymous mutation rates average 1% per my, with non-synonymous changes being about seven times less frequent. Over 1.1 million indels were detected and phylogenetically polarized, revealing a two-fold bias toward deletions over small insertions. We suggest that this genome down-sizing bias counteracts genome size growth by TE amplification and insertions, and helps explain the relatively small genomes that are restricted to this subgenus. Compared to the rate of nucleotide substitution, the rate of indel occurrence is much lower averaging about 17 nucleotide substitutions per indel event

MOLECULAR BIOLOGY AND PHYSIOLOGY Fiber Initiation in 18 Cultivars and Experimental Lines of Three Gossypium Species

ABSTRACT A new technique was developed to study the cotton fiber initiation process and fiber initial densities. The goal was to provide an additional tool to cotton breeders and geneticists interested in fiber improvement. The objectives were to assess whether fiber initiation patterns reported for some Gossypium hirsutum L. and G. barbadense L. cultivars extend to a more diverse range of cultivars/lines; and to test if there is a relationship between fiber initials density, lint percentage, and fiber characteristics. This study was performed with 17 cultivars and experimental lines of G. hirsutum (upland cotton) and G. barbadense (Pima cotton) and one G. arboreum L. accession. The ovules were extracted from flowers at the day of anthesis and 1 and 2 d thereafter, stained with a fluorescent dye, DiOC 6 (3) (3,3′-dihexyloxacarbocyanine iodide), and observed under a light microscope. Staining cotton fiber initials with DiOC 6 (3) enabled the evaluation of a greater number of samples than the more time-consuming scanning electron microscopy protocols to assess the fiber initiation process. There were significant differences in fiber initial densities among cultivars and lines but these did not cluster into &quot;upland&quot; and &quot;Pima&quot; types as had been expected. Upland and Pima fiber initiation occurred at anthesis, whereas Sea Island Pima initiation was delayed a day. A delay in fiber initiation was also confirmed in fuzzless mutant lines. Fiber initial densities were not found to be useful predictors of lint percentage

Kepler Flares II: The Temporal Morphology of White-Light Flares on GJ 1243

We present the largest sample of flares ever compiled for a single M dwarf, the active M4 star GJ 1243. Over 6100 individual flare events, with energies ranging from $10^{29}$ to $10^{33}$ erg, are found in 11 months of 1-minute cadence data from Kepler. This sample is unique for its completeness and dynamic range. We have developed automated tools for finding flares in short-cadence Kepler light curves, and performed extensive validation and classification of the sample by eye. From this pristine sample of flares we generate a median flare template. This template shows that two exponential cooling phases are present during the white-light flare decay, providing fundamental constraints for models of flare physics. The template is also used as a basis function to decompose complex multi-peaked flares, allowing us to study the energy distribution of these events. Only a small number of flare events are not well fit by our template. We find that complex, multi-peaked flares occur in over 80% of flares with a duration of 50 minutes or greater. The underlying distribution of flare durations for events 10 minutes and longer appears to follow a broken power law. Our results support the idea that sympathetic flaring may be responsible for some complex flare events.Comment: 12 pages, 9 figures, accepted for publication in Ap

Perancangan Peraga LED Terprogram Berbasis Mikrokontroler AT89C52

Dengan tersedianya mikrokontroler yang memiliki berbagai fasilitas serta murahnya harga PC yang ditawarkan, maka peluang untuk merancang peralatan pengendalian LED untuk berbagai keperluan menjadi sangat terbuka. Tujuan dari penelitian ini adalah merancang dan menguji peraga LED terprogram berbasis mikrokontroler AT89C52. Alat penampil LED matrik dirancang data-nya bisa dimasukan secara otomatis, sehingga LED dapat menampilkan data dengan segera. Perancangan sistem penampil LED matrik yang dibuat meliputi dua bagian utama yaitu bagian perangkat keras dan bagian perangkat lunak. Perangkat keras meliputi mikrokontroler AT89C52 sebagai pusat pengontrol, penggerak kolom dan penggerak baris serta LED matrik untuk menampilkan data. Perangkat lunak meliputi bahasa mesin mikrokontroler dan untuk berhubungan dengan PC menggunakan Borland Delphi. Pengujian dilakukan dengan membandingkan tampilan LED matrik dengan data masukan dari PC. Alat ini dapat mengendalikan dan menampilkan LED sesuai data yang diberikan. LED matrik dapat menampilkan empat baris teks yang masing-masing baris maksimal enam karakter, gambar serta animasi running text (teks berjalan)

Identification and genomic location of a reniform nematode (Rotylenchulus reniformis) resistance locus (Renari) introgressed from Gossypium aridum into upland cotton (G. hirsutum)

In this association mapping study, a tri-species hybrid, [Gossypium arboreum × (G. hirsutum × G. aridum)2], was crossed with MD51ne (G. hirsutum) and progeny from the cross were used to identify and map SSR markers associated with reniform nematode (Rotylenchulus reniformis) resistance. Seventy-six progeny (the 50 most resistant and 26 most susceptible) plants were genotyped with 104 markers. Twenty-five markers were associated with a resistance locus that we designated Renari and two markers, BNL3279_132 and BNL2662_090, mapped within 1 cM of Renari. Because the SSR fragments associated with resistance were found in G. aridum and the bridging line G 371, G. aridum is the likely source of this resistance. The resistance is simply inherited, possibly controlled by a single dominant gene. The markers identified in this project are a valuable resource to breeders and geneticists in the quest to produce cotton cultivars with a high level of resistance to reniform nematode

Diversity analysis of cotton (Gossypium hirsutum L.) germplasm using the CottonSNP63K Array

Cotton germplasm resources contain beneficial alleles that can be exploited to develop germplasm adapted to emerging environmental and climate conditions. Accessions and lines have traditionally been characterized based on phenotypes, but phenotypic profiles are limited by the cost, time, and space required to make visual observations and measurements. With advances in molecular genetic methods, genotypic profiles are increasingly able to identify differences among accessions due to the larger number of genetic markers that can be measured. A combination of both methods would greatly enhance our ability to characterize germplasm resources. Recent efforts have culminated in the identification of sufficient SNP markers to establish high-throughput genotyping systems, such as the CottonSNP63K array, which enables a researcher to efficiently analyze large numbers of SNP markers and obtain highly repeatable results. In the current investigation, we have utilized the SNP array for analyzing genetic diversity primarily among cotton cultivars, making comparisons to SSR-based phylogenetic analyses, and identifying loci associated with seed nutritional traits. (Résumé d'auteur