Analysis of the DNA methylation of maize (Zea mays L.) in response to cold stress based on methylation-sensitive amplified polymorphisms

2013 ◽  
Vol 56 (1) ◽  
pp. 32-38 ◽  
Author(s):  
Xiaohui Shan ◽  
Xiaoyu Wang ◽  
Guang Yang ◽  
Ying Wu ◽  
Shengzhong Su ◽  
...  
2019 ◽  
Vol 50 (Special) ◽  
Author(s):  
Shenawa & Alfalahi

Methylation Sensitive Amplification Polymorphism (MSAP) was used to characterize the alterations in DNA methylation in maize (Zea mays L.) inbred lines and their half-daillels affected by plant densities (213333 plant h-1 and 13333 plant h-1). The two restriction was enzymes ( HpaII and MspI) succeeded in diagnosing a total of 23 specific loci, most of (22 loci) were Methylation Sensitive Loci (MSL), while the only one NML (No Methylated Loci) was monomorphic. Thirteen out of 22 MSL loci polymorphic, recording a were polymorphism percentage of 59%. Results of FeSOD gene expression cleared the different response of maize inbreds and hybrids to high plant density stress. Generally, the expression of  the targeted gene was increased in plants submitted to high plant density stress compared with low density. The inbred 3 and its single hybrid 1×3 achieved the highest level of gene expression under high planting density (5505.7 and 21098.6 copy, respectively), meanwhile, inbred 5 and it's single hybrid 4×5 gained the maximum level of FeSOD expression at the low plant density (8317.6 and 6862.1 copy, respectively). The response reached to its maximum limit in many of those genotypes, some other genotypes showed relatively steady performance along with higher stress, such as parent 1, that gave the lowest number of gene copies in both, high and low plant density (1375.8 and 1569.5 copy, respectively).


Genes ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1638
Author(s):  
Joram Kiriga Waititu ◽  
Quan Cai ◽  
Ying Sun ◽  
Yinglu Sun ◽  
Congcong Li ◽  
...  

Cold tolerance is a complex trait that requires a critical perspective to understand its underpinning mechanism. To unravel the molecular framework underlying maize (Zea mays L.) cold stress tolerance, we conducted a comparative transcriptome profiling of 24 cold-tolerant and 22 cold-sensitive inbred lines affected by cold stress at the seedling stage. Using the RNA-seq method, we identified 2237 differentially expressed genes (DEGs), namely 1656 and 581 annotated and unannotated DEGs, respectively. Further analysis of the 1656 annotated DEGs mined out two critical sets of cold-responsive DEGs, namely 779 and 877 DEGs, which were significantly enhanced in the tolerant and sensitive lines, respectively. Functional analysis of the 1656 DEGs highlighted the enrichment of signaling, carotenoid, lipid metabolism, transcription factors (TFs), peroxisome, and amino acid metabolism. A total of 147 TFs belonging to 32 families, including MYB, ERF, NAC, WRKY, bHLH, MIKC MADS, and C2H2, were strongly altered by cold stress. Moreover, the tolerant lines’ 779 enhanced DEGs were predominantly associated with carotenoid, ABC transporter, glutathione, lipid metabolism, and amino acid metabolism. In comparison, the cold-sensitive lines’ 877 enhanced DEGs were significantly enriched for MAPK signaling, peroxisome, ribosome, and carbon metabolism pathways. The biggest proportion of the unannotated DEGs was implicated in the roles of long non-coding RNAs (lncRNAs). Taken together, this study provides valuable insights that offer a deeper understanding of the molecular mechanisms underlying maize response to cold stress at the seedling stage, thus opening up possibilities for a breeding program of maize tolerance to cold stress.


2013 ◽  
Vol 33 (2) ◽  
pp. 363-371 ◽  
Author(s):  
Víctor M. Rodríguez ◽  
Ana Butrón ◽  
Mohamed O. A. Rady ◽  
Pilar Soengas ◽  
Pedro Revilla

2014 ◽  
Vol 36 (6) ◽  
pp. 1529-1537 ◽  
Author(s):  
Filiz Aygun Erturk ◽  
Guleray Agar ◽  
Esra Arslan ◽  
Gokce Nardemir ◽  
Zehra Sahin

Agronomie ◽  
1982 ◽  
Vol 2 (2) ◽  
pp. 159-166 ◽  
Author(s):  
Olivier BETHENOD ◽  
Christine JACOB ◽  
Jean-Claude RODE ◽  
Jean-François MOROT-GAUDRY
Keyword(s):  
Zea Mays ◽  

1970 ◽  
Vol 3 (2) ◽  
pp. 318-326
Author(s):  
Yoyon Riono.
Keyword(s):  
Zea Mays ◽  

Penelitian tentang pengaruh pemberian produktivitas pupuk organik terhadap hasil Tanaman Jagung (Zea mays L) di tanah mineral penelitian ini di laksanakan pada bulan Februari sampai Mei, yang bertempat di Sungai Salak Kecsmstsn Tempuling Kabupaten Indragiri Hilir Provinsi Riau. Penelitian ini menggunakan Rancangan Acak Kelompok (RAK) yang disusun secara faktorial yang terdiri dari 2 faktor dan 3 ulangan. Faktor B adalah bokashi pupuk kandang yang terdiri dari 4 taraf yaitu B0 (tanpa pemberianpupuk kandang), B1 (5 ton/ha) dan B2 (10 tom/ ha), serta B3 (15 ton/ha) Parameter yang di amati adalah tinggi tanaman, panjang daun ke tujuh, berat brangkasan basah, berat berangkasan kering, berat tongkol pertanaman sampel, diameter tongkol , produksi per plot, dan berat 100 biji. Selanjutnya data yang di peroleh di olah secara statistik, apabila F hitung lebih besar dari F tabel di lanjutkan dengan uji lanjut Tukey HSD pada taraf 5%. Hasil penelitian menunjukan bahwa interaksi bokashi pupuk kandang dan varietas berpengaruh nyata terhadap berat tongkol dan produksi dan produksi per plot, akan tetapi tidak berpengaruh nyata terhadap tinggi tanaman, panjang daun ke tujuh, berat brangkasan basah, berat brangkasan kering , diameter tongkol dan berat 1000 biji. Untuk perlakuan bokashi pupuk kandang secara tunggal berpengaruh nyata terhadap terhadap diameter tongkol , akan tetapi tidak berpengaruh nyata terhadap tinggi tanaman, panjang daun ke tujuh, berat brangkasan basah, berat brangkasan kering, berat tongkol, produksi per plot, dan berat 1000 biji, perlakuan bokashi terbaik terdapat pada pemberian 15 ton/ha. Sedangkan perlakuan varietas secara tunggal berpengaruh nyata terhadap berat brangkasan basah, berat tongkol, dan produksi per plot seta berat 1000 biji, akan tetapi tidak berbeda nyata dengan tinggi tanaman, panjang daun ke tujuh, berat brangkasan kering, dan diameter tongkol. Varietass terbaik adalah NT 10


Sign in / Sign up

Export Citation Format

Share Document