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| 1 | Levels of Crotonaldehyde and 4-hydroxy-(E)-2-nonenal and Expression of Genes Encoding Carbonyl-Scavenging Enzyme at Critical Node During Rice Seed Aging显示文摘The critical node(CN) is an important stage during seed aging, which is related to effective genebank conservation. Previous studies have demonstrated that proteins undergo carbonylated modification at the CN in rice, indicating oxidative damage. However, the levels of reactive carbonyl species(RCS) and the associated scavenging system at the CN are largely unknown. In this study, we optimized methods for the extraction and analysis of RCS from dry rice embryos. In order to acquire seeds at the CN, rice seeds were subjected to natural conditions for 7, 9, 11 and 13 months, and the seed germination rates were reduced to 90%, 82%, 71% and 57%, respectively. We chose the stage with seed germination rate of 82% as the CN according to the rice seed vigor loss curve. The levels of crotonaldehyde and 4-hydroxy-(E)-2-nonenal(HNE) were significantly increased at the CN. In addition, genes encoding carbonyl-scavenging enzyme, including Os ALDHs and Os AKRs, were significantly down-regulated at the CN, and reductions in the expression of Os ALDH2-2, Os ALDH2-5, Os ALDH3-4, Os ALDH7, Os AKR1 and Os AKR2 in particular could be responsible for RCS accumulation. Thus, the accumulations of crotonaldehyde and HNE and down-regulation of genes encoding carbonyl-scavenging enzyme might be related to an accelerating loss of seed viability at the CN. | FU Shenzao YIN Guangkun XIN Xia WU Shuhua WEI Xinghua LU Xinxiong | 2018 | Rice science2018，25，3： | 3 |
| 2 | Effects of Seed Viability and Number of Generations on Genetic Integrity of Soybean Germplasm Zhonghuang 18 by AFLP Markers显示文摘The seeds of a soybean cultivar Zhonghuang 18 were subjected to accelerated aging for 0(population G_0-1), 112(population G_0-2), 154(population G_0-3) and 196 d(population G_0-4), whose germination percentage was found to be 98.0%, 95.0%, 81.0%, and 79.0%, respectively. Then, the four populations were regenerated twice in the field. The first descendant populations were marked as G_1-1, G_1-2, G_1-3 and G_1-4, and the second were marked as G_2-1, G_2-2, G_2-3 and G_2-4, respectively. The genetic variation between the control population(G_0-1) and the experimental populations was analyzed using 12 AFLP primer combinations. The results showed that there was no significant difference in genetic similarity between the 11 experimental populations and the control population G_0-1. The genetic similarity between population G_2-4 and G_0-1 was still as high as 0.933 3, indicating that the F_2 generation of the population whose germination percentage was only 79.0% still had a high genetic similarity to the control population. The results of t-tests revealed that the populations G_1-1, G_2-1, G_1-2 and G_2-2 showed no significant difference from the control population G_0-1 in effective number of alleles per locus(Ae), genetic diversity index(H) and Shannon's diversity index(I), while these indices of populations G_0-3, G_0-4, G_1-3, G_1-4, G_2-3 and G_2-4 were significantly reduced. χ~2 tests indicated that the populations G_1-1 and G_2-1 showed little difference, and the populations G_0-2, G_0-3, G_0-4, G_1-2, G_1-3, G_1-4, G_2-2, G_2-3, and G_2-4 showed great difference in allele frequency distribution from the control population G_0-1, and the difference was greater when the seed viability was lower. Compared with the control population G_0-1, the number of rare alleles(Nr) of the populations G_0-2, G_1-1, G_2-1, G_1-2 and G_2-2 showed no significant difference, while that of the populations G_0-3, G_0-4, G_1-3, G_1-4, G_2-3 and G_2-4 declined obviously. These results revealed that compared with the control population, the genetic diversity and Nr for the descendant populations of the populations with 98.0% and 95.0% germination percentages did not change significantly, but declined greatly for the descendant populations of the populations with 81.0.% and 79.0% percentages. The results suggested that the decline in seed viability has a greater impact than the number of generations on genetic structure of soybean germplasm. So, it is suggested that soybean seed with an initial germination percentage of 98.0% should be regenerated before its germination percentage declines to 81.0%. | Dong WANG Xiaodong ZHANG Runfang LI Lingyun LU Xiaomu WANG Xiaohong GU Xia XIN Guangkun YIN Xinxiong LU Hanfeng DING | 2019 | Agricultural Biotechnology2019，8，2： | 0 |
| 3 | Effects of Seed Vitality and Regeneration on Genetic Integrity in Soybean by SSR Markers显示文摘The seeds of Zhonghuang 18 were selected as a test material,and subjected to artificial aging treatment(0,112,154 and 196 d),obtaining four 4 populations,i.e.,G_0-1,G_0-2,G_0-3 and G_0-4,the germination rates of which were 98.0%,95.0%,81.0%and 79.0%,respectively.The four populations were reproduced twice in field,giving four populations of the first reproduced generation G_1-1,G_1-2,G_1-3 and G_1-4 and four populations of the second reproduced generation G_2-1,G_2-2,G_2-3 and G_2-4.The results showed that the number of alleles(Ae)per locus and genetic identity of all the treatment populations did not change significantly compared with the control population G_0-1,and population G_0-4 still shared 0.996 2 genetic identity with the control population,indicating that the genetic identity between the population with a germination rate of 79.0%and the control population was still high.The results of t test showed that populations G_0-2,G_1-1 and G_2-1 showed number of alleles per locus(A),genetic diversity index(H)and Shannon index without significantly differences from the control population G_0-1;populations G_1-2 and G_2-2 had the number of alleles per locus(A)significantly decreased;and the above genetic diversity parameters of populations G_0-3,G_0-4,G_1-3,G_1-4,G_2-3 and G_2-4 decreased significantly or very significantly.The results ofχ~2test showed that there were almost no differences in the allelic frequency distribution between populations G_0-2,G_1-1 and G_2-1 and the control populaiton G_0-1;and populations G_0-3,G_0-4,G_1-2,G_1-3,G_1-4,G_2-2,G_2-3and G_2-4 differed in allele frequency distribution,and the lower the vitality level,the greater the differences.Compared with the control population G_0-1,populations G_0-2,G_1-1 and G_2-1 had no significant changes in number of rare alleles,while populations G_0-3,G_0-4,G_1-2,G_2-2,G_1-3,G_1-4,G_2-3 and G_2-4 decreased significantly in number of rare alleles.The above results showed that compared with the control population,the progeny populations reproduced from the population with a germination rate of 98.0%had significant changes in genetic diversity and number of rare alleles,while the values of the progeny populations reproduced from populations having germination rates of 81.0%and 79.0%,respectively,decreased significantly,and the number of alleles per locus and number of rare alleles of the progeny populations reproduced from the population with a germination rate of 95.0%began to decrease.The decline in viability has a greater effect on the genetic structure of soybean germplasm populations than reproduction generation.It is recommended that the germination rate standard for regeneration of soybean germplasm with an initial germination rate of 98.0%should not be lower than 81.0%. | Dong WANG Xiaodong ZHANG Runfang LI Lingyun LU Xiaomu WANG Xiaohong GU Xia XIN Guangkun YIN Xinxiong LU Hanfeng DING | 2019 | Agricultural Biotechnology2019，8，1： | 0 |
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