Autofluorescence and Fluorochrome Staining of Alveolar Lining1

2015 ◽  
pp. 77-88
Author(s):  
J. D. Hackney ◽  
C. R. Collier ◽  
D. E. Rounds
Keyword(s):  
Fluorochrome Staining

Comparative Karyotype Investigations in the European Crayfish Astacus astacus and A. leptodactylus (Decapoda, Astacidae)

Crustaceana ◽  
2011 ◽  
Vol 84 (12-13) ◽  
pp. 1497-1510 ◽  
Author(s):  
M. Pavlica ◽  
M. Mcžić ◽  
G. Klobučar ◽  
M. Šrut ◽  
I. Maguire ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Chromosome Complement ◽  
Size Difference ◽  
45S Rdna ◽  
Astacus Astacus ◽  
Fluorochrome Staining ◽  
Rdna Sites ◽  
Freshwater Habitats ◽  
Acrocentric Chromosomes

AbstractThis study reports on the chromosome number and karyological characteristics of the endangered species of European crayfish, Astacus astacus and A. leptodactylus (Decapoda, Astacidae), both native to Croatian freshwater habitats. The karyotype of A. astacus and A. leptodactylus consists of 2n = 176 and 2n = 180 chromosomes, respectively. The haploid chromosome complement of A. astacus consists of 52 metacentric, 35 metacentric-submetacentric, and 1 acrocentric chromosomes. Fluorochrome staining with 4,6-diamino-2-phenylindole (DAPI) has revealed that the karyotypes of A. astacus and A. leptodactylus are characterized by large heterochromatic blocks located at centromeric and intercalary positions on the chromosomes. Interstitial heterochromatic blocks were more frequent in A. astacus than in A. leptodactylus. In both species pairing of chromosomes in meiosis was regular with the majority of bivalents in a ring- and a dumbbell-form. Fluorescence in situ hybridization (FISH) has revealed that two 45S rDNA loci were present in the investigated species. In A. astacus one of the two 45S rDNA-bearing chromosome pairs was highly heteromorphic, exhibiting a three-fold size difference between 45S rDNA sites on homologous chromosomes. Such a size difference was significantly less pronounced in A. leptodactylus. The karyotype differences between A. astacus and A. leptodactylus suggest changes in chromosome number as well as position of repetitive DNAs have played a role in the karyotype evolution of the species of Astacus.

Insights into chromosomal evolution of Cicadomorpha using fluorochrome staining and mapping 18S rRNA and H3 histone genes

2018 ◽  
Vol 57 (2) ◽  
pp. 314-322 ◽  
Author(s):  
Allison Anjos ◽  
Andressa Paladini ◽  
Olivia Evangelista ◽  
Diogo C. Cabral‐de‐Mello
Keyword(s):  
18S Rrna ◽  
Chromosomal Evolution ◽  
Histone Genes ◽  
Fluorochrome Staining

scholarly journals Comparative molecular cytogenetics in Melipona Illiger species (Hymenoptera, Apidae)

Sociobiology ◽  
2018 ◽  
Vol 65 (4) ◽  
pp. 696 ◽  
Author(s):  
Vanderly Andrade-Souza ◽  
Olivia Maria Pereira Duarte ◽  
Cinthia Caroline Cardoso Martins ◽  
Igor Silva Santos ◽  
Márcio Gilberto Cardoso Costa ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Chromosome Number ◽  
Fluorescent In Situ Hybridization ◽  
Molecular Cytogenetics ◽  
Fluorochrome Staining ◽  
Rdna Sites ◽  
Cytogenetic Studies ◽  
Melipona Species ◽  
Almost All

Cytogenetic studies in Melipona are scarce with only 24 species analyzed cytogenetically. Of these, six species had the rDNA sites physically mapped and characterized by Fluorescent in situ Hybridization (fish). The aim of this study was to perform karyotype analyzes on Melipona species from different regions of Brazil, with a greater sampling representative of the Amazonian fauna and using conventional, fluorochrome staining and FISH with heterologous rDNA probes. The predominant chromosome number was 2n = 18, however, the subspecies M. seminigra abunensis and M. s. pernigra showed 2n = 22 chromosomes. The karyotypes were symmetrical, however M. bicolor, M. quadrifasciata, M. flavolineata, M. fuscopilosa, M. nebulosa presented the first pair heteromorphic in length. CMA3+ blocks also exhibited heteromorphism of size and in almost all cases coincided with rDNA sites, except for M. crinita and M. nebulosa, which presented additional non-coincident CMA3+ blocks. The CMA/ rDNA sites were terminal and interstitial in species with high heterochromatic content, and pericentromeric in those species with low heterochromatic content. In addition to pointing out cytogenetic features of cytotaxonomic importance, the reorganization of the genome in Melipona is discussed.

Paracentric Inversions Differentiate the Conservative Karyotypes in Two Centropomus Species (Teleostei: Centropomidae)

2019 ◽  
Vol 157 (4) ◽  
pp. 239-248 ◽  
Author(s):  
Amanda T. Borges ◽  
Marcelo B. Cioffi ◽  
Luiz A.C. Bertollo ◽  
Rodrigo X. Soares ◽  
Gideão W.W.F. Costa ◽  
...  
Keyword(s):  
Economic Value ◽  
5S Rdna ◽  
Chromosomal Evolution ◽  
Chromosomal Mapping ◽  
Rdna Site ◽  
Fluorochrome Staining ◽  
Western Atlantic ◽  
Replication Banding ◽  
Evolutionary Diversification ◽  
Paracentric Inversions

Centropomus is the sole genus of the Centropomidae family (Teleostei), comprising 12 species widely distributed throughout the Western Atlantic and Eastern Pacific, with 6 of them occurring in the Western Atlantic in extensive sympatry. Their life history and phylogenetic relationships are well characterized; however, aspects of chromosomal evolution are still unknown. Here, cytogenetic analyses of 2 Centropomus species of great economic value (C. undecimalis and C. mexicanus) were performed using conventional (Giemsa, Ag-NOR, and fluorochrome staining, C- and replication banding) and molecular (chromosomal mapping of 18S and 5S rDNA, H2A-H2B and H3 hisDNA, and (TTAGGG)n repeats) approaches. The karyotypes of both species were composed of 48 solely acrocentric chromosomes (2n = 48; FN = 48), but the single ribosomal site was located in varying positions in the long arms of the second largest chromosome pair. Replication bands were generally similar, although conspicuous differences were observed in some chromosome regions. In both species, the histone H3 genes were located on 3 apparently homeologous chromosome pairs, but the exact position of these clusters differed slightly. Interspecific hisDNA and rDNA site displacements can indicate the occurrence of multiple paracentric inversions during the evolutionary diversification of the Centropomus genomes. Although the karyotypes remained similar in both species, our data demonstrate an unsuspected microstructural reorganization between them, driven most likely by a series of paracentric inversions.

scholarly journals Association of methionyl-tRNA synthetase with detergent-insoluble components of the rough endoplasmic reticulum.

1983 ◽  
Vol 96 (4) ◽  
pp. 1138-1147 ◽  
Author(s):  
C V Dang ◽  
D C Yang ◽  
T D Pollard
Keyword(s):  
Endoplasmic Reticulum ◽  
Fluorescent Antibody ◽  
Insoluble Fraction ◽  
Trna Synthetase ◽  
Insoluble Residue ◽  
Synthetase Activity ◽  
Fluorochrome Staining ◽  
Antibody Staining ◽  
Triton X ◽  
Methionyl Trna Synthetase

Using fluorescent antibody staining, we have established the association of methionyl-tRNA synthetase with the endoplasmic reticulum in PtK2 cells. After Triton X-100 extraction, 70% of the recovered aminoacyl-tRNA synthetase activity was found in the detergent-insoluble fraction. This fraction of the enzyme remained localized with insoluble endoplasmic reticulum antigens and with ribosomes, which were stained with acridine orange. By both fluorescence microscopy and electron microscopy the organization of the detergent-insoluble residue was found to depend on the composition of the extracting solution. After extraction with a microtubule-stabilizing buffer containing EGTA, Triton X-100, and polyethylene glycol (Osburn, M., and K. Weber, 1977, Cell, 12:561-571) the ribosomes were aggregated in large clusters with remnants of membranes. After extraction with a buffer containing Triton X-100, sucrose, and CaCl2 (Fulton, A. B., K. M. Wang, and S. Penman, 1980, Cell, 20:849-857), the ribosomes were in small clusters and there were few morphologically recognizable membranes. In both cases the methionyl-tRNA synthetase and some endoplasmic reticulum antigens retained approximately their normal distribution in the cell. Double fluorochrome staining showed no morphological association of methionyl-tRNA synthetase with the microtubule, actin, or cytokeratin fiber systems of PtK2 cells. These observations demonstrate that detergent-insoluble cellular components, sometimes referred to as "cytoskeletal" preparations, contain significant amounts of nonfilamentous material including ribosomes, and membrane residue. Caution is required in speculating about intermolecular associations in such a complex cell fraction.

Fatigue Microdamage in Bovine Trabecular Bone

2003 ◽  
Vol 125 (6) ◽  
pp. 769-776 ◽  
Author(s):  
Tara L. A. Moore ◽  
Lorna J. Gibson
Keyword(s):  
Trabecular Bone ◽  
Compressive Strain ◽  
Staining Technique ◽  
Area Fraction ◽  
Maximum Strain ◽  
Yield Strain ◽  
Fluorochrome Staining ◽  
Microdamage Accumulation ◽  
Small Cracks ◽  
Fatigue Microdamage

Microdamage, in the form of small cracks, may accumulate in trabecular bone loaded in fatigue. Specimens of bovine trabecular bone were loaded in compressive fatigue at one of four normalized stresses and loading was stopped after the specimens reached one of six maximum strains. Microdamage was identified using a fluorochrome staining technique, and microdamage parameters, including the number of damaged trabeculae and the damaged area fraction, were measured. No microdamage was observed during loading to strains below the yield strain; at higher strains, all microdamage parameters increased with increasing maximum compressive strain. Few significant differences were observed in the type or amount of microdamage accumulation between specimens loaded to the same maximum strain at different normalized stresses; however, more trabecular fractures were observed at high numbers of cycles, which corresponded to low normalized stresses.

Haemadsorption Followed by Fluorochrome Staining

BMJ ◽  
1963 ◽  
Vol 2 (5349) ◽  
pp. 98-100 ◽  
Author(s):  
S. C. Arya
Keyword(s):  
Fluorochrome Staining
Sign in / Sign up

Export Citation Format

Share Document