PHYSICAL MAPPING AND INHERITANCE STUDIES OF CRY1AC GENE ON TRANSGENIC COTTON CHROMOSOMES

2005 ◽  
Vol 40 (2) ◽  
pp. 206-210
Author(s):  
Yu Cheng Zhu ◽  
John J. Adamczyk

Transgenic cotton (Gossypium hirsutum L.) containing a modified cry1Ac gene from the soil bacterium Bacillus thuringiensis Berliner has been widely adopted for suppression of lepidopterous pests. As of 2004, over 90% of the cotton acreage in the mid-southern United States contained this modified cry1Ac gene. We developed a technique using the polymerase chain reaction (PCR) for routine detection of the cry1Ac gene in transgenic cotton plants. A total of eight cry1Ac genes were aligned for the PCR primer design. A DNA fragment was amplified from transgenic cotton, sequenced, and confirmed to be a portion of the cry1Ac gene. A total of 150 cotton plants representing four cultivars were examined for the presence of the cry1Ac gene. Results demonstrated that all of these cotton plants harbored the cry1Ac gene (i.e., 100% purity). This PCR technique can be used for future studies involving the expression of cry1Ac gene as well as corresponding protein expression.


2015 ◽  
Vol 04 (02) ◽  
Author(s):  
Mehboob Ur Rahman ◽  
Muhammad Zaman ◽  
Yusuf Zafar ◽  
Zulfiqar Hayder ◽  
Amer Jamil ◽  
...  

Genetics ◽  
1999 ◽  
Vol 153 (4) ◽  
pp. 1701-1708 ◽  
Author(s):  
Martin Beye ◽  
Greg J Hunt ◽  
Robert E Page ◽  
M Kim Fondrk ◽  
Lore Grohmann ◽  
...  

Abstract Sex determination in Hymenoptera is controlled by haplo-diploidy in which unfertilized eggs develop into fertile haploid males. A single sex determination locus with several complementary alleles was proposed for Hymenoptera [so-called complementary sex determination (CSD)]. Heterozygotes at the sex determination locus are normal, fertile females, whereas diploid zygotes that are homozygous develop into sterile males. This results in a strong heterozygote advantage, and the sex locus exhibits extreme polymorphism maintained by overdominant selection. We characterized the sex-determining region by genetic linkage and physical mapping analyses. Detailed linkage and physical mapping studies showed that the recombination rate is <44 kb/cM in the sex-determining region. Comparing genetic map distance along the linkage group III in three crosses revealed a large marker gap in the sex-determining region, suggesting that the recombination rate is high. We suggest that a “hotspot” for recombination has resulted here because of selection for combining favorable genotypes, and perhaps as a result of selection against deleterious mutations. The mapping data, based on long-range restriction mapping, suggest that the Q DNA-marker is within 20,000 bp of the sex locus, which should accelerate molecular analyses.


Author(s):  
Arthur Mayrink Elizeu ◽  
Natalia Martins Travenzoli ◽  
Riudo de Paiva Ferreira ◽  
Denilce Meneses Lopes ◽  
Mara Garcia Tavares

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