62 research outputs found
Nucleases isolated from Chelidonium majus L. milky sap can induce apoptosis in human cervical carcinoma HeLa cells but not in Chinese Hamster Ovary CHO cells.
Detection and seasonal expression pattern of a pathogenesis-related protein (PR-10) in Douglas-fir ( Pseudotsuga menziesii
Molecular mapping of the Pinus monticola Cr2 gene using AFLP and SCAR markers
<p>White pine blister rust (WPBR), caused by Cronartium ribicola, is a devastating disease in five-needle pines. Genetic resistance is an important component of integrated strategies to control WPBR. The major resistance gene Cr2, discovered by Kinloch et<br />al.(1999), is also effective against British Columbia (BC) isolates of WPBR (Hunt et al. 2004). Pyramiding Cr2 gene with other resistance<br />genes is being pursued as a strategy in BC white pine breeding. To facilitate this strategy, we have recently identified a few RAPD markers<br />linked to Cr2 at one side (Liu et al. 2006). The objective of the present study was to identify amplified fragment length polymorphism<br />(AFLP) markers linked to both sides of Cr2 for its more precise apping. Use of the AFLP technique combined with bulked segregant analysis (BSA) and haploid segregation analysis allowed the identification of five AFLP markers. Of these five AFLP markers in the Cr2 linkage, markers EacccMccgat-365, EactgMcccac- 290, and EacagEacag-750 were<br />linked in coupling and EacagMcccag-160r and EacccMccgat-180r in repulsion. Following cloning and sequencing of the AFLP and<br />RAPD markers, specific PCR primers were designed and used in the amplification of sequence characterized amplified region<br />(SCAR) markers at both sides of Cr2. EacccMccgat- 365 and RAPD marker U570-843 reported previously were converted into SCAR<br />markers. These two SCARs segregated in a 1:1 (presence:absence) ratio and the scoring cosegregated with their respective AFLP or<br />RAPD marker. The SCAR marker EacccMccgat- 365-scar was positioned at 3.1 Kosambi cM from one side of Cr2 and U570-843-scar<br />localized at 1.4 Kosambi cM from other side. Both SCAR markers can be useful in breeding programs with marker-assisted selection procedure<br />to screen for resistance. This study represents the first report of the development of PCR-based sequence-specific markers linked<br />to blister rust resistance in five-needle pines. These findings may improve the precision of molecular breeding for blister rust resistance<br />and could be the staging point for isolating the Cr2 gene.</p
Immunochemical characterization of a high molecular weight basic allergen (HMBA) of rye grass (Lolium perenne) pollen
The Effect of rhBMP-7 on Distraction Osteogenesis of the Rabbit Mandible
Note:The water extract of timothy grass pollen (WSG) was fractionated by a combination of different methods, i.e. salt precipitation, ion-exchange chromatography and gel-filtration on Sephadex. The most active fraction (C-IV) was found to be 100,000 times more potent than WSG and contained all the skinactive components of WSG. Fraction C-IV contained 3 of the 7 antigenic components of WSG, as demonstrated by immunoelectrophoresis. WSG gave two groups of precipitin lines with rabbit anti-WSG antiserum, which were identified as the 'outer' and 'inner' bands on immunodiffusion; the antigenic components of fraction C-IV were shown to belong to the 'inner' groups of antigen of WSG. […
Allergenic cross-reactivity of cytochromes c of Kentucky bluegrass and perennial ryegrass pollens
Ultrastructural localization of chitin in the five spore stages of the blister rust fungus, Cronartium ribicola
An immunoelectrophoretic analysis of the allergens of Cynodon dactylon (Bermuda grass) pollen
- …