scholarly journals Meiotic behaviour and morpho-phenological variation in cut stock (Matthiola incana L.) flower

2017 ◽  
Vol 29 (1) ◽  
pp. 51-61 ◽  
Author(s):  
Sepideh Famil Irani ◽  
Mostafa Arab
Keyword(s):  
Genetic Background ◽  
Basic Chromosome Number ◽  
Meiotic Abnormalities ◽  
Matthiola Incana ◽  
Additional Chromosome ◽  
Diakinesis Stage ◽  
Different Genetic Background ◽  
A Chain ◽  
First Time ◽  
Meiotic Anomalies

AbstractMorpho-phenological and meiotic studies were performed in twelve cultivars of Matthiola incana. All of the cultivars were diploid (2n = 2x = 14) with basic chromosome number x = 7. A number of aneuploid PMCs (n + 1) were observed in plants of two cultivars, named ‘Nobel’ (NB) and ‘Goddess’ (GD), at the diakinesis stage. Trisomic individuals with the frequency of 20% and 5% and (2n + 1 = 15) somatic chromosomes were observed in seeds obtained from single-flowered plants of the cultivars NB and GD, respectively. An additional chromosome was mostly observed in the form of a chain trivalent or a rod univalent. Various meiotic abnormalities were found in all the cultivars to different degrees. In these cultivars, the percentage of cells with meiotic abnormalities was higher in anaphase I. Cytomixis was observed for the first time in Matthiola incana. ANOVA tests revealed significant differences in morpho-phenological characteristics. ‘Nobel’ differs from the others in all of the vegetative features investigated in this study. All the cultivars studied except ‘Nobel’ and ‘Pacific Crimson’ possessed high pollen fertility (> 90%). Five groups of the cultivars based on morpho-phenological features disagree with the clustering of cultivars based on meiotic traits. It is thought that the various morpho-phenological features observed among the cultivars could be due to their different genetic background and not only to meiotic anomalies.

scholarly journals Cytotaxonomic Study of Hypodematium (Hypodematiaceae) from China

Phytotaxa ◽  
2014 ◽  
Vol 161 (2) ◽  
pp. 101 ◽  
Author(s):  
Renxiang Wang ◽  
Wen Shao ◽  
Ling Liu
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Habitat Preferences ◽  
Northeast Asia ◽  
Basic Chromosome Number ◽  
Basic Chromosome ◽  
Dry Conditions ◽  
Diakinesis Stage ◽  
First Time ◽  
Meiosis I

Chromosome numbers and reproductive biology of nine species of the fern genus Hypodematium (Hypodematiaceae) from China were investigated. The chromosome numbers of eight species are reported here for the first time: H. daochengensis n=41 (41 II); H. fordii n=40 (40 II), n=80 (40 II+40 I), 2n=120; H. glanduloso-pilosum n=41 (41 II), 2n=82, 2n=123; H. gracile n=41 (41 II); H. hirsutum n= 41 (41 II); H. microleptoides n=41 (41 II); H. sinense n= 40 (40 II) and H. squamuloso-pilosum n=41 (41 II). Two cytotypes, n=82 (41 II+41 I) and 2n=123 in H. crenatum, are reported for the first time.  Our results showed that the species with these cytotypes are agamospermous triploids: H. crenatum n = 82 (41 II +41 I), H. glanduloso-pilosum n = 82 (41 II +41 I) and H. fordii n = 80 (40 II +40 I), based on the unequal size and presence of aborted spores in the sporangium, and the allotriploid hybrid chromosomes in the spore mother cell at the diakinesis stage of meiosis I. The remaining species are sexual diploids and tetraploids, based on the chromosome number n = 41 and n =82 at the diakinesis stage of meiosis I of spore mother cells. The relationships among habitat preferences, frond hairs and reproductive modes in Hypodematium are discussed and illustrated. It appears that plants with large fronds and sparse, thin hairs, living in humid and shady places undergo sexual reproduction, while small plants living in sunny and dry conditions with thick hairs undergo agamospermous reproduction. The distribution pattern and basic chromosome number all indicated the basic chromosome number x= 41 was plesiomorphic, whereas x=40 was apomorphic. Chromosome aneuploid changes occurred in this genus. The distribution of the sexual diploids and tetraploids and agamospermous triploids suggests that the genus might have originated in the Himalayas and dispersed from there to northeast Asia and Japan.

scholarly journals A resource to explore the discovery of rare diseases and their causative genes

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Friederike Ehrhart ◽  
Egon L. Willighagen ◽  
Martina Kutmon ◽  
Max van Hoften ◽  
Leopold M. G. Curfs ◽  
...  
Keyword(s):  
Rare Disease ◽  
Rare Diseases ◽  
Genetic Background ◽  
Gene Discovery ◽  
Google Scholar ◽  
Semantic Model ◽  
Causative Gene ◽  
Scientific Publications ◽  
Monogenic Diseases ◽  
First Time

AbstractHere, we describe a dataset with information about monogenic, rare diseases with a known genetic background, supplemented with manually extracted provenance for the disease itself and the discovery of the underlying genetic cause. We assembled a collection of 4166 rare monogenic diseases and linked them to 3163 causative genes, annotated with OMIM and Ensembl identifiers and HGNC symbols. The PubMed identifiers of the scientific publications, which for the first time described the rare diseases, and the publications, which found the genes causing the diseases were added using information from OMIM, PubMed, Wikipedia, whonamedit.com, and Google Scholar. The data are available under CC0 license as spreadsheet and as RDF in a semantic model modified from DisGeNET, and was added to Wikidata. This dataset relies on publicly available data and publications with a PubMed identifier, but by our effort to make the data interoperable and linked, we can now analyse this data. Our analysis revealed the timeline of rare disease and causative gene discovery and links them to developments in methods.

scholarly journals Identification and Characterization of Novel Maize Mirnas Involved in Different Genetic Background

2015 ◽  
Vol 11 (7) ◽  
pp. 781-793 ◽  
Author(s):  
Lei Sheng ◽  
Wenbo Chai ◽  
Xuefeng Gong ◽  
Lingyan Zhou ◽  
Ronghao Cai ◽  
...  
Keyword(s):  
Genetic Background ◽  
Different Genetic Background ◽  
Identification And Characterization

Functionality of cryopreserved juvenile ovaries from mutant mice in different genetic background strains after allotransplantation

Cryobiology ◽  
2010 ◽  
Vol 60 (2) ◽  
pp. 129-137 ◽  
Author(s):  
Kuo-Yu Huang ◽  
Suzanna A. de Groot ◽  
Henri Woelders ◽  
Gijsbertus T.J. van der Horst ◽  
Axel P.N. Themmen ◽  
...  
Keyword(s):  
Genetic Background ◽  
Mutant Mice ◽  
Different Genetic Background

scholarly journals Phenotypic and clonal stability of antigen-inexperienced memory-like T cells across the genetic background, hygienic status, and aging

2020 ◽  
Author(s):  
Alena Moudra ◽  
Veronika Niederlova ◽  
Jiri Novotny ◽  
Lucie Schmiedova ◽  
Jan Kubovciak ◽  
...  
Keyword(s):  
Gene Expression ◽  
T Cells ◽  
Genetic Background ◽  
Expression Profiles ◽  
Bacterial Colonization ◽  
Gene Expression Profiles ◽  
Inbred Strains ◽  
Microbial Colonization ◽  
Independent Manner ◽  
Different Genetic Background

AbstractAntigen-inexperienced memory-like T (AIMT) cells are functionally unique T cells representing one of the two largest subsets of murine CD8+ T cells. However, differences between laboratory inbred strains, insufficient data from germ-free mice, a complete lack of data from feral mice, and unclear relationship between AIMT cells formation during aging represent major barriers for better understanding of their biology. We performed a thorough characterization of AIMT cells from mice of different genetic background, age, and hygienic status by flow cytometry and multi-omics approaches including analyses of gene expression, TCR repertoire, and microbial colonization. Our data showed that AIMT cells are steadily present in mice independently of their genetic background and hygienic status. Despite differences in their gene expression profiles, young and aged AIMT cells originate from identical clones. We identified that CD122 discriminates two major subsets of AIMT cells in a strain-independent manner. Whereas thymic CD122LOW AIMT cells (innate memory) prevail only in young animals with high thymic IL-4 production, peripheral CD122HIGH AIMT cells (virtual memory) dominate in aged mice. Co-housing with feral mice changed the bacterial colonization of laboratory strains, but had only minimal effects on the CD8+ T-cell compartment including AIMT cells.

Isolation of telomere DNA from Neurospora crassa

1987 ◽  
Vol 7 (9) ◽  
pp. 3168-3177
Author(s):  
M G Schechtman
Keyword(s):  
Linkage Group ◽  
Neurospora Crassa ◽  
Genetic Background ◽  
Type Strain ◽  
Wild Type Strain ◽  
The Other ◽  
Wild Type ◽  
Oak Ridge ◽  
Entire Chromosome ◽  
Different Genetic Background

The most distal known gene on Neurospora crassa linkage group VR, his-6, was cloned. A genomic walk resulted in isolation of the telomere at VR. It was obtained from a library in which the endmost nucleotides of the chromosome had not been removed by nuclease treatment before being cloned, and mapping indicates that the entire chromosome end has probably been cloned. Sequences homologous to the terminal 2.5 kilobases of DNA from VR from these Oak Ridge N. crassa strains are found at other sites in the genome. To characterize these sites, I crossed an Oak Ridge-derived his-6 strain with a wild-type strain of different genetic background (Mauriceville) and characterized the hybridization patterns seen in the progeny. It appears that the sequences homologous to the VR terminus are found at genetically different sites in the two parental strains, and no hybridization to the VR telomere from Mauriceville was detected. The other genomic copies identified in the Oak Ridge parent were not telomeres. I suggest that any repeating sequence blocks found immediately adjacent to the VR terminus in Oak Ridge strains must be small and that the repeating element identified in that background may be an N. crassa transposable element integrated near the the chromosome end at VR.

Microstrip Gas Counters

2014 ◽  
pp. 31-51
Keyword(s):  
Glass Surface ◽  
Two Dimensional ◽  
Large Area ◽  
Proportional Chamber ◽  
Microelectronic Technology ◽  
Multiwire Proportional Chamber ◽  
Dimensional Version ◽  
A Chain ◽  
New Generation ◽  
First Time

In this chapter, the first micropattern gaseous detector, the microstrip gas counter, invented in 1988 by A. Oed, is presented. It consists of alternating anode and cathode strips with a pitch of less than 1 mm created on a glass surface. It can be considered a two-dimensional version of a multiwire proportional chamber. This was the first time microelectronic technology was applied to manufacturing of gaseous detectors. This pioneering work offers new possibilities for large area planar detectors with small gaps between the anode and the cathode electrodes (less than 0.1 mm). Initially, this detector suffered from several serious problems, such as charging up of the substrate, discharges which destroyed the thin anode strips, etc. However, by efforts of the international RD28 collaboration hosted by CERN, most of them were solved. Although nowadays this detector has very limited applications, its importance was that it triggered a chain of similar developments made by various groups, and these collective efforts finally led to the creation of a new generation of gaseous detectors-micropattern detectors.

Meiotic chromosome behaviour in Cenchrus ciliaris

Bothalia ◽  
1998 ◽  
Vol 28 (1) ◽  
pp. 83-90 ◽  
Author(s):  
N. C. Visser ◽  
J. J. Spies
Keyword(s):  
Chromosome Number ◽  
Meiotic Chromosome ◽  
Basic Chromosome Number ◽  
Chromosome Behaviour ◽  
Meiotic Abnormalities ◽  
Single Specimen ◽  
Cenchrus Ciliaris ◽  
Basic Chromosome ◽  
Single Genome ◽  
Meiotic Irregularities

A basic chromosome number of x = 9 has been confirmed for Cenchrus ciliaris L. Polyploidy is common and levels vary from tetraploid to hexaploid. Aneuploidv is reported for a single specimen, where two chromosomes of a single genome were lost. Various meiotic irregularities were observed. The highest incidence of meiotic abnormalities was observed in the pentaploid specimens. This was attributed to their uneven polyploid level All specimens varied from segmental alloploid to alloploid.

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