The experiment on individual chromosome assignments and chromosomal diversity was conducted using a multi-probe fluorescence in situ hybridization (FISH) system in D subgenome of tetraploid Gossypium barbadense (D(b)), G. thurberi (D(1)) and G. trilobum (D(8)), which the later two were the possible subgenome donors of tetraploid cottons. The FISH probes contained a set of bacterial artificial chromosome (BAC) clones specific to 13 individual chromosomes from D subgenome of G. hirsutum (D(h)), a D genome centromere-specific BAC clone 150D24, 45S and 5S ribosomal DNA (rDNA) clones, respectively. All tested chromosome orientations were confirmed by the centromere-specific BAC probe. In D(1) and D(8), four 45S rDNA loci were found assigning at the end of the short arm of chromosomes 03, 07, 09 and 11, while one 5S rDNA locus was successfully marked at pericentromeric region of the short arm of chromosome 09. In D(b), three 45S rDNA loci and two 5S rDNA loci were found out. Among them, two 45S rDNA loci were located at the terminal of the short arm of chromosomes D(b)07 and D(b)09, whilst one 5S rDNA locus was found situating near centromeric region of the short arm of chromosome D(b)09. The positions of the BAC clones specific to the 13 individual chromosomes from D(h) were compared between D(1), D(8) and D(b). The result showed the existence of chromosomal collinearity within D(1) and D(8), and as well between them and D(b). The results will serve as a base for understanding chromosome structure of cotton and polyploidy evolution of cotton genome and will provide bio-information for assembling the sequences of finished and the on-going cotton whole genome sequencing projects.
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http://dx.doi.org/10.1266/ggs.86.165 | DOI Listing |
Acta Parasitol
January 2025
Veterinary Laboratories, PAAFR, P.O. Box: 21422, Safat, Kuwait, 13075, Kuwait.
Purpose: The objective of the study was to establish the prevalence of Sarcocystis (Apicomplexa, Sarcocystidae) in brown rats from Jleeb Al-Shuyoukh, Kuwait, and to describe detected parasites using morphological and DNA analysis methods.
Methods: Ninety-eight brown rats (Rattus norvegicus) were examined for Sarcocystis spp. Obtained sarcocysts were investigated using light microscopy and electron microscopy.
IMA Fungus
December 2024
Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN, USA.
Multicopy nuclear ribosomal DNA (rDNA) genes have been used as markers for fungal identification for three decades. The rDNA sequences in a genome are thought to be homogeneous due to concerted evolution. However, intragenomic variation of rDNA sequences has recently been observed in many fungi, which may make fungal identification and species abundance estimation based on these loci problematic.
View Article and Find Full Text PDFPlant Dis
December 2024
Korea University, Environmental Science & Ecological Engineering, Seoul, Seoul, Korea (the Republic of), 02841;
Cerastium glomeratum Thuill., known as sticky mouse-ear chickweed, is native to Europe and has become naturalized in the wild on most continents. After its accidental introduction to Korea around the 1980s, it quickly became one of the dominant invasive weeds on the Korean peninsula and is now considered a significant threat to the Korean agroecosystem (Park et al.
View Article and Find Full Text PDFPlant Dis
December 2024
Ningbo Academy of Agricultural Sciences, Institute of Vegetables, Ningbo yinzhou District dehou street NO.19, Ningbo , Zhejiang, China, 315040;
In May of 2024, a stem soft rot disease in melon (Cucumis melo L.) was observed in Ningbo (29.52°N, 121.
View Article and Find Full Text PDFHarmful Algae
January 2025
Bachok Marine Research Station, Institute of Ocean and Earth Sciences, University of Malaya 16310 Bachok, Kelantan, Malaysia. Electronic address:
The benthic pennate diatom Nitzschia navis-varingica, known for producing domoic acid (DA) and its isomers, is widely distributed in the Western Pacific (WP) region. To investigate the genetic differentiation and gene flow patterns among the populations in the WP, the genetic diversity of 354 strains of N. navis-varingica was analysed using two nuclear-encoded rDNA loci: the large subunit rDNA (LSU rDNA) and the internal transcribed spacer 2 (ITS2).
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