As a study of the allelopathy of multiplier onion(Allium cepa var. aggregatum)on the reproductive development in garlic(Allium sativum),‘Yining Hongpi’garlic and‘M-4’bolting multiplier onion were used to examine the effect on garlic flowering through mixed intercropping. The results showed that bolting multiplier onion significantly enhanced the growth potential of garlic. The mean plant height and pseudostem diameter were 96.3 cm and 10.6 mm respectively and increased significantly by 6.1 cm,2.4 mm compared with control group. Bolting multiplier onion promoted the reproductive development in garlic. The bolting time was advanced by 4 days under allelopathic treatment in comparison with the control group. The number of functional florets per inflorescence increased,meanwhile the number and size of topsets decreased. The transcriptional levels of the floral meristem identity genes gaLFY and AsFUL were up-regulated. Bolting multiplier onion had allelopathic effects on garlic by promoting the functional flower development to potentially restore fertility.
In order to explore the role of AmMYB2 in the betalain synthesis in Amaranthus tricolor,the bioinformatics,gene expression and functional analysis of AmMYB2(Genbank accession No. KY814751.1)in the red amaranth cultivar‘Dahong’were conducted. The results showed that the open reading frame(ORF)of the AmMYB2 is 678 bp in length. The coding protein molecular mass fraction is 25.96 kD,which belongs to R2R3 MYB transcription factor with R2R3 MYB domain. Subcellular localization assay revealed that the AmMYB2 protein was localized in the nucleus. Nucleotide sequence analysis revealed that the AmMYB2 is relatively close to betalain synthesis-related BvMYB1 and AmMYB1,with an identity of 62.11% and 49.93%,respectively. Quantitative real-time PCR(qRT-PCR)results showed that the expression level of AmMYB2 was higher in red amaranth cultivar than that in green,and was different in different tissues and the different parts of leaves from the‘Dahong’amaranth,consistent with the proportional to the content of betalains. After the over expression vector of AmMYB2 was constructed and transferred to tobacco and Arabidopsis thaliana,the expression level of AmMYB2 was higher in both plants,without color changes. Therefore,the AmMYB2 may be a positive regulatory factor for the synthesis of betalains in amaranth,and maybe not involved in anthocyanin synthesis.
miRNAs are small non-coding RNAs of 20–24 nt widely present in eukaryotes and play important roles in plant growth and stress adaptation. Water spinach(Ipomoea aquatica)can tolerate prolonged high temperature. However,miRNAs in water spinach have not yet been identified and their role in long-time high temperature is still unknown. In this paper,taking highly heat-resistant‘Taiguo Sancha’and poorly heat-resistant‘Liuye’as material,two high-quality sRNA pools were constructed after treatment with 42 ℃ for 15 days. The number of high-quality sequences both exceeded 17.3 Mb,and the number of 24 nt clean reads in‘Taiguo Sancha’was much higher than that of‘Liuye’. After comparison with water spinach’s transcriptome,1 363 258 and 1 629 209 sequences were obtained respectively. The two libraries shared 1 047 133(11.36%)unique reads,indicating that sRNAs varied in cultivars with different heat resistance. A total of 71 miRNAs were identified in water spinach,of which 22 were differentially expressed. The target genes were predicted by TargetFinder and a sum of 233 target genes were obtained. In addition,water spinach‘Bendi Sancha’with strong-heat-resistance and weakly heat-resistant‘Zhuye’were used as materials to study the expression levels of pre-miR160,pre-miR166,pre-miR172,pre-miR393,and pre-miR3627 that were differentially expressed after long-time high temperature treatment. The results showed that the expression of pre-miR160-2 in‘Bendi Sancha’and‘Zhuye’increased significantly,but in different levels;the expression of miR166 was decreased in‘Bendi Sancha’but increased significantly in‘Zhuye’;miR172 could be induced by high temperature,however,there was no difference in the two cultivars;the expression of miR3627 was decreased in‘Bendi Sancha’after high temperature treatment while there was no obvious change in‘Zhuye’. The difference in the expression patterns of miRNA precursors suggests that the mechanism of miRNA is different during long-term high temperature in water spinach.
In order to solve the problem of low water and nutrient conserving capacity of sandy soil,five-year-old Fuji/Malus hupeheusis Rehd. was taken as material to study the effects of biochar and compost on soil water and nutrient conserving capacity and apple growth. The results showed the percentage of high quality fruit,single apple fruit weight and apple yield of biochar combined with chemical fertilizer were 70.21%,261.92 g and 59.62 kg,respectively,increasing by 43.40%,15.21% and 36.06%,respectively,compared with the single hole application of chemical fertilizer treatment(control). The content of fruit soluble solids and vitamin C increased by 7.10% and 30.30%,respectively. Biochar combined with chemical fertilizer increased soil available nitrogen,available potassium,being 153.58 and 142.2 mg ? kg-1,respectively,which increased by 15.69% and 33.27%,compared with the conventional fertilization treatment. On the third days after precipitation,soil water content of biochar application was 36.65% and 27.92% higher than that of upper and lower soil layers respectively. After one month evaporation,the soil water was still 56.65% and 45.79% higher than the upper and lower soil layers,respectively. The results showed that the combination of biochar and chemical fertilizer had significant effects on soil water,nutrient content,yield and quality of apple fruit in sandy soil.
NPR1 is one of important regulatory factors inducing expression of desease-resistant genes,and mainly acts in the up- or down-streams on salicylic acid signal transduction pathway. Full-length cDNAs of NPR1 homologous genes were screened from enriched full-length normalized cDNA library by pool-dilued PCR method in Nai’s leaves;young leaves in one-year grafted seedlings were sprayed with salicylic acid solutions of different concentrations,the differences in expression levels of the isolated NPR1 genes were detected by fluorescence quantitative PCR. The results showed that 4 full-length cDNAs of NPR1 homologous genes were obtained and named as PsNPR1,PsNPR3.1,PsNPR3.2 and PsNPR3.3 respectively;their responding full lengths were 2 442,1 827,2 244 and 2 615 bp;their reponding lengths of ORFs were 1 788,1 770,1 767 and 1 782 bp,encoding proteins containing 596,590,589 and 594 amino acids,respectively;the results of amino acid sequence alignment showed that coding regions of the 4 NPR1 homologous genes contained two conservative domains(BTB/POZ and ANK)and nuclear localization signal(NLS);Nai’s PsNPR1 was clustered with Arabidopsis thaliana’s AtNPR1 and AtNPR2 forming a cluster,Nai’s PsNPR3.1,PsNPR3.2 and PsNPR3.3 were clustered with Arabidopsis thaliana’s AtNPR3 and AtNPR4 forming another cluster. The expression level of PsNPR1 was the highest in Nai’s young leaves sprayed with 1.0 mmol ? L-1 salicylic acid solutions;the expression levels of PsNPR1,PsNPR3.1 and PsNPR3.2 continuously increased in process of response to 1.0 mmol ? L-1 salicylic acid,and reached maximum at 30 hours after spraying,then tended to decrease,therefore,the optimal spraying concentration of salicylic acid was 1.0 mmol ? L-1,the optimal responsing time of 1.0 mmol ? L-1 salicylic acid was 30 hours.
The banana cultivars are originated from intra- and interspecific hybridization of two wild diploid species:Musa acuminate Colla and Musa balbisiana Colla,contributing the A and B genomes,respectively. The B genome contains important and good genes. A sequence characterized amplified region(SCAR)marker was successfully developed from the inter-retrotransposon amplified polymorphism (IRAP)marker named gypsy-IRAP related to banana B genome,and it was found to be able to identificate B genome of banana cultivars with different genotypes such as AAw,BB,AAcv,ABB,AAB,AAAB.