Identification and Analysis of R2R3-MYB Genes in Sweet Potato Genome

Author(s):  
Xiaofang Huang ◽  
Chuyun Bi ◽  
Bifang Huang ◽  
Ming Xu ◽  
Zhijian Yang ◽  
...  
Keyword(s):  
Nature Plants ◽  
2017 ◽  
Vol 3 (9) ◽  
pp. 696-703 ◽  
Author(s):  
Jun Yang ◽  
M-Hossein Moeinzadeh ◽  
Heiner Kuhl ◽  
Johannes Helmuth ◽  
Peng Xiao ◽  
...  
Keyword(s):  

Biomolecules ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 317 ◽  
Author(s):  
Xiaoxu Li ◽  
Cun Guo ◽  
Salman Ahmad ◽  
Qi Wang ◽  
Jing Yu ◽  
...  

The MYB proteins represent a large family of transcription factors and play important roles in development, senescence, and stress responses in plants. In the current study, 233 MYB transcription factor-encoding genes were identified and analyzed in the potato genome, including 119 R1-MYB, 112 R2R3-MYB, and two R1R2R3-MYB members. R2R3-MYB is the most abundant MYB subclass and potato R2R3-MYB members together with their Arabidopsis homologs were divided into 35 well-supported subgroups as the result of phylogenetic analyses. Analyses on gene structure and protein motif revealed that members from the same subgroup shared similar exon/intron and motif organization, further supporting the results of phylogenetic analyses. Evolution of the potato MYB family was studied via syntenic analysis. Forty-one pairs of StMYB genes were predicted to have arisen from tandem or segmental duplication events, which played important roles in the expansion of the StMYB family. Expression profiling revealed that the StMYB genes were expressed in various tissues and several StMYB genes were identified to be induced by different stress conditions. Notably, StMYB030 was found to act as the homolog of AtMYB44 and was significantly up-regulated by salt and drought stress treatments. Furthermore, overexpression of StMYB030 in Arabidopsis enhanced salt stress tolerance of transgenic plants. The results from this study provided information for further functional analysis and for crop improvements through genetic manipulation of these StMYB genes.


Genome ◽  
2011 ◽  
Vol 54 (7) ◽  
pp. 603-609
Author(s):  
Tom Okpul ◽  
Robert M. Harding ◽  
Mark J. Dieters ◽  
Ian D. Godwin

Retrotransposons are a class of transposable elements that represent a major fraction of the repetitive DNA of most eukaryotes. Their abundance stems from their expansive replication strategies. We screened and isolated sequence fragments of long terminal repeat (LTR), gypsy-like reverse transcriptase (rt) and gypsy-like envelope (env) domains, and two partial sequences of non-LTR retrotransposons, long interspersed element (LINE), in the clonally propagated allohexaploid sweet potato (Ipomoea batatas (L.) Lam.) genome. Using dot-blot hybridization, these elements were found to be present in the ~1597 Mb haploid sweet potato genome with copy numbers ranging from ~50 to ~4100 as observed in the partial LTR (IbLtr-1) and LINE (IbLi-1) sequences, respectively. The continuous clonal propagation of sweet potato may have contributed to such a multitude of copies of some of these genomic elements. Interestingly, the isolated gypsy-like env and gypsy-like rt sequence fragments, IbGy-1 (~2100 copies) and IbGy-2 (~540 copies), respectively, were found to be homologous to the Bagy-2 cDNA sequences of barley (Hordeum vulgare L.). Although the isolated partial sequences were found to be homologous to other transcriptionally active elements, future studies are required to determine whether they represent elements that are transcriptionally active under normal and (or) stressful conditions.


2020 ◽  
Vol 46 (8) ◽  
pp. 1195-1207
Author(s):  
Cai-Xiao LIANG ◽  
Yuan-Yuan SHI ◽  
Xiao-Fang HUANG ◽  
Li-Xiang ZHOU ◽  
Shi-Qiang LIN ◽  
...  

2020 ◽  
Author(s):  
Hanna Amoanimaa-Dede ◽  
Jiacheng Zhang ◽  
Chuntao Su ◽  
Hongbo Zhu

Abstract The genetic complexity and the lack of genomic resources in sweet potato make genetic improvement extremely challenging. Simple sequence repeats (SSRs) offer an effective molecular marker technology for molecular-based breeding and for locating important loci in crop plants, but only a few have previously been developed in sweet potato. To explore new SSR markers and accelerate its use in sweet potato, we developed a set of 2,431 primer pairs from 133,727 SSRs identified in the sweet potato genome using the Perl script MISA software. The average frequency was one SSR per 6.26 kb with dinucleotides (38.5%) being the most dominant repeat motif. The main motif types in all repeats were AT/AT, AAT/ATT, A/T, AAAT/ATTT, AAAAT/ATTTT and AAAAAT/ATTTTT accounting for 78.29% of the total SSRs. Out of the 100 randomly selected primer pairs, 50% produced clear bands and amplified 251 alleles. On average, the number of alleles was 5.02 per locus for values ranging from 1 to 13 alleles. The UPGMA cluster analysis grouped the 24 sweet potato materials into four clusters at a similarity coefficient of 0.68 showing no relationship between the genotypes and the geographic sources of germplasm. The SSR markers currently developed will provide valuable genetic resources for germplasm identification, and accelerate studies on genetic diversity in sweet potato and related species.


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
D Rosas-Ramírez ◽  
R Pereda-Miranda
Keyword(s):  

2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Musdar Musdar ◽  
Lukmanul Hakim ◽  
Juliani Juliani ◽  
Jailani Jailani

White sweet potato starch (Ipomea batatas L.) and avocado seed starch (Parsea americana Mill) derived from local plants have the potential to be developed as agricultural products. Starch is a hydrocolloid compound as a potential local resource to be utilized. Glycerol function as an anti-freezing which is hygroscopic. This study aims to determine the ratio of white sweet potato starch with avocado seed starch and the concentration of glycerol for making edible film. This study was an experiment using a completely randimized factorial design with 2 (two) main factor consisting of a comparison of white sweet potato starch and avocado seed with 3 levels: P1 = 35%:65%., P2=50%:50%., P3=65%:35% and glycerol concentration with 3 levels: G1=1%., G2=2%., G3=3%. The best result reasearch were content of 23.03% (tratment P1G1), solubility of 55.57% (treatment P3G2)., swelling test of 9.83% (treatment P2g3)., elongation of 8.18% (treatment P3G2)


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