Correction to “CF2–II Alternative Splicing Isoform Regulates the Expression of Xenobiotic Tolerance-Related Cytochrome P450 CYP6CY22 in Aphis gossypii Glover”
{"title":"Correction to “CF2–II Alternative Splicing Isoform Regulates the Expression of Xenobiotic Tolerance-Related Cytochrome P450 CYP6CY22 in Aphis gossypii Glover”","authors":"Yaping Ding, Jianyi Li, Kunpeng Yan, Long Jin, Chengcheng Fan, Rui Bi, Haoran Kong, Yiou Pan, Qingli Shang","doi":"10.1021/acs.jafc.4c11996","DOIUrl":null,"url":null,"abstract":"A corrected version of Figure 9 appears below. An incorrect image appeared in the negative control in the original version. No bacteria could grow in medium lacking Leu with ABA (600 ng/mL) in the negative control. This correction does not change the scientific conclusions of the article. Figure 9. Structure of the <i>CYP6CY22</i> promoter region. (A) Structure of the 5′-flanking region of <i>CYP6CY22</i>. The TSS in the figure represents the transcription start site. The transcription starting point number is +1, with the upstream sequence starting with “–” and the downstream sequence starting with “+”. The predicted <i>CF</i><sub>2</sub><i>–II-AS</i> protein binding sites and mutant sequence are indicated. (B) Investigation of the interaction between <i>CYP6CY22.p</i> and <i>CF</i><sub>2</sub><i>–II-AS</i> by the Y1H assay. Yeast transformants containing the <i>CYP6CY22.p</i> vector and TF plasmid were selected on SD/-Leu media supplemented with ABA. Positive control: yeast strain transformed with the pGADT7-<i>p53</i> and pAbAi-<i>p53</i> plasmids; negative control: yeast strain transformed with pAbAi-<i>CYP6CY22.p</i>. This article has not yet been cited by other publications.","PeriodicalId":41,"journal":{"name":"Journal of Agricultural and Food Chemistry","volume":"77 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Agricultural and Food Chemistry","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1021/acs.jafc.4c11996","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
A corrected version of Figure 9 appears below. An incorrect image appeared in the negative control in the original version. No bacteria could grow in medium lacking Leu with ABA (600 ng/mL) in the negative control. This correction does not change the scientific conclusions of the article. Figure 9. Structure of the CYP6CY22 promoter region. (A) Structure of the 5′-flanking region of CYP6CY22. The TSS in the figure represents the transcription start site. The transcription starting point number is +1, with the upstream sequence starting with “–” and the downstream sequence starting with “+”. The predicted CF2–II-AS protein binding sites and mutant sequence are indicated. (B) Investigation of the interaction between CYP6CY22.p and CF2–II-AS by the Y1H assay. Yeast transformants containing the CYP6CY22.p vector and TF plasmid were selected on SD/-Leu media supplemented with ABA. Positive control: yeast strain transformed with the pGADT7-p53 and pAbAi-p53 plasmids; negative control: yeast strain transformed with pAbAi-CYP6CY22.p. This article has not yet been cited by other publications.
期刊介绍:
The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.