Isolation and chromosomal distribution of a novel Ty1-copia-like sequence fromSecale, which enables identification of wheat—Secale africanum introgression lines

2009 ◽  
Vol 50 (1) ◽  
pp. 25-28 ◽  
Author(s):  
J. Jia ◽  
Z. Yang ◽  
G. Li ◽  
Ch. Liu ◽  
M. Lei ◽  
...  
Genome ◽  
2012 ◽  
Vol 55 (11) ◽  
pp. 765-774 ◽  
Author(s):  
Meng-Ping Lei ◽  
Guang-Rong Li ◽  
Cheng Liu ◽  
Zu-Jun Yang

Wild Secale species, Secale africanum Stapf., serve as a valuable source for increasing the diversity of cultivated rye (Secale cereale L.) and provide novel genes for wheat improvement. New wheat – S. africanum chromosome 1Rafr addition, 1Rafr(1D) substitution, 1BL.1RafrS and 1DS.1RafrL translocation, and 1RafrL monotelocentric addition lines were identified by chromosome banding and in situ hybridization. Disease resistance screening revealed that chromosome 1RafrS carries resistance gene(s) to new stripe rust races. Twenty-nine molecular markers were localized on S. africanum chromosome 1Rafr by the wheat – S. africanum introgression lines. Twenty markers can also identically amplify other reported wheat – S. cereale chromosome 1R derivative lines, indicating that there is high conservation between the wild and cultivated Secale chromosome 1R. Nine markers displayed polymorphic amplification between S. africanum and S. cereale chromosome 1Rafr derivatives. The comparison of the nucleotide sequences of these polymorphic markers suggested that gene duplication and sequence divergence may have occurred among Secale species during its evolution and domestication.


Euphytica ◽  
2013 ◽  
Vol 194 (2) ◽  
pp. 197-205 ◽  
Author(s):  
Meng-Ping Lei ◽  
Guang-Rong Li ◽  
Li Zhou ◽  
Cheng-Hui Li ◽  
Cheng Liu ◽  
...  

2010 ◽  
Vol 5 (2) ◽  
pp. 187-192 ◽  
Author(s):  
Juqing Jia ◽  
Guangrong Li ◽  
Cheng Liu ◽  
Jianping Zhou ◽  
Zujun Yang

Author(s):  
Jason R. Swedlow ◽  
Neil Osheroff ◽  
Tim Karr ◽  
John W. Sedat ◽  
David A. Agard

DNA topoisomerase II is an ATP-dependent double-stranded DNA strand-passing enzyme that is necessary for full condensation of chromosomes and for complete segregation of sister chromatids at mitosis in vivo and in vitro. Biochemical characterization of chromosomes or nuclei after extraction with high-salt or detergents and DNAse treatment showed that topoisomerase II was a major component of this remnant, termed the chromosome scaffold. The scaffold has been hypothesized to be the structural backbone of the chromosome, so the localization of topoisomerase II to die scaffold suggested that the enzyme might play a structural role in the chromosome. However, topoisomerase II has not been studied in nuclei or chromosomes in vivo. We have monitored the chromosomal distribution of topoisomerase II in vivo during mitosis in the Drosophila embryo. This embryo forms a multi-nucleated syncytial blastoderm early in its developmental cycle. During this time, the embryonic nuclei synchronously progress through 13 mitotic cycles, so this is an ideal system to follow nuclear and chromosomal dynamics.


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