scholarly journals Nucleus

2021 ◽  
Author(s):  
Noorah Abdulaziz Othman Alkubaisi ◽  
Nagwa Mohammed Amin Aref

In our application of AuNPs on the leaf surface, we were pushing the Barley Yellow Dwarf Virus (BYDV-PAV) source and Gold nanoparticles (AuNPs) into the plant cell system up on the events of systemic plant defense response. In the infected host cell, the viral coat protein is the first obvious in the cytoplasm. When nanoparticles are applied on leaf surfaces, a large surface area relative to their volume happens. AuNPs solutions are more active and dispersed ooplasm. The correlation between Zeta potential value and Zeta sizer is inverse proportion. Filaments are visible in the nucleopores, the nuclear outline is distorted, and massive clumping of heterochromatin begins as declared. It was mostly found in or around regions of ribosome-associated filaments. Our present study combines TEM and nucleus content in the presence of AuNPS to explore the level of repair mechanism illustrating in TEM micrographs, showing Polyploidy nucleus and segregated chromatin. Multi membranous structure, imaging the AuNPs inside and around the nucleus and Pseudo crystal array is enveloped in an endoplasmic reticulum cisterna (ER).

Crop Science ◽  
1990 ◽  
Vol 30 (5) ◽  
pp. 1008 ◽  
Author(s):  
J. Collin ◽  
A. Comeau ◽  
C.A. St-Pierre

Crop Science ◽  
1994 ◽  
Vol 34 (2) ◽  
pp. 371-375 ◽  
Author(s):  
Ellen M. Bauske ◽  
Frederic L. Kolb ◽  
Adrianna D. Hewings ◽  
Gordon Cisar

Genome ◽  
2004 ◽  
Vol 47 (6) ◽  
pp. 1114-1121 ◽  
Author(s):  
Shu-Mei Jiang ◽  
Long Zhang ◽  
Jun Hu ◽  
Rui Shi ◽  
Guang-He Zhou ◽  
...  

The alien addition line TAI-27 contains a pair of chromosomes of Thinopyrum intermedium that carry resistance against barley yellow dwarf virus (BYDV). A subtractive library was constructed using the leaves of TAI-27, which were infected by Schizaphis graminum carrying the GAV strain of BYDV, and the control at the three-leaf stage. Nine differentially expressed genes were identified from 100 randomly picked clones and sequenced. Two of the nine clones were highly homologous with known genes. Of the remaining seven cDNA clones, five clones matched with known expressed sequence tag (EST) sequences from wheat and (or) barley whereas the other two clones were unknown. Five of the nine differentially expressed sequences (WTJ9, WTJ11, WTJ15, WTJ19, and WTJ32) were highly homologous (identities >94%) with ESTs from wheat or barley challenged with pathogens. These five sequences and another one (WTJ18) were also highly homologous (identities >86%) with abiotic stress induced ESTs in wheat or barley. Reverse Northern hybridization showed that seven of the nine differentially expressed cDNA sequences hybridized with cDNA of T. intermedium infected by BYDV. Three of these also hybridized with cDNA of line 3B-2 (a parent of TAI-27) infected by BYDV. The alien chromosome in TAI-27 was microdissected. The second round linker adaptor mediated PCR products of the alien chromosomal DNA were labeled with digoxygenin and used as the probe to hybridize with the nine differentially expressed genes. The analysis showed that seven differentially expressed genes were homologous with the alien chromosome of TAI-27. These seven differentially expressed sequences could be used as ESTs of the alien chromosome of TAI-27. This research laid the foundation for screening and cloning of new specific functional genes conferring resistance to BYDV and probably other pathogens.Key words: suppression subtractive hybridization (SSH), expressed sequence tag (EST), linker adaptor mediated polymerase chain reaction (LA-PCR), chromosome microdissection.


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