Identification of Candidate Transcripts Related to Drought Stress using Secondary Traits and qRT-PCR in Tropical Maize (Zea mays L.)Identification of Candidate Transcripts Related to Drought Stress using Secondary Traits and qRT-PCR in Tropical Maize (Zea mays L.)
- Other Titles
- Identification of Candidate Transcripts Related to Drought Stress using Secondary Traits and qRT-PCR in Tropical Maize (Zea mays L.)
- Authors
- 김효철; 송기태; 문준철; 김재윤; 김경희; 이병무
- Issue Date
- Dec-2019
- Publisher
- 한국작물학회
- Keywords
- De novo; drought stress; maize; qRT-PCR; secondary trait
- Citation
- 한국작물학회지, v.64, no.4, pp 432 - 440
- Pages
- 9
- Indexed
- KCI
- Journal Title
- 한국작물학회지
- Volume
- 64
- Number
- 4
- Start Page
- 432
- End Page
- 440
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/7341
- DOI
- 10.7740/kjcs.2019.64.4.432
- ISSN
- 0252-9777
2287-8432
- Abstract
- Global climate change exerts adverse effects on maize production. Among abiotic stresses, drought stress duringthe tasseling stage (VT) can increase anthesis-silking intervals (ASI) and decrease yield. We performed an evaluation of ASI andyield using a drought-sensitive line (Ki3) and a drought-tolerant line (Ki11) to analyze the correlation with ASI and yield.
Moreover, the de novo data of Ki11 were analyzed to find putative novel transcripts related todrought stress in tropical maize. Atotal of 182 transcripts, with a log2 ratio >1.5, were found by comparing drought conditions to a control. The top 40 transcripts ofhigh expression levels in the de novo analysis were selected and analyzed with PCR. Of the 40 transcripts, six novel transcriptswere detected by quantitative real-time PCR (qRT-PCR) using seedling and VT stage samples. Five transcripts (transcripts_1, 12,34, 35, and 40) were up-regulated in the Ki11 shoot at seedling stage, and transcripts_1, 12, and 40 were up-regulated at there-watering stage after 12 h of drought stress. The transcripts_32 and 34 were up-regulated at the VT stage. Hence, transcript_34possibly plays a significant role in drought tolerance during the seedling and VT stages. The transcript_32 was identified aschloramphenicol acetyltransferase (CAT) by Pfam domain analysis. The function of the other transcripts remained unknown.
Further characterization of these novel transcripts in genetic regulation will be of great value for the improvement of maizeproduction.
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