Cytochrome P450 proteins, widely distributed multifunctional enzymes, are mainly involved in biosynthetic and degradative pathways of endogenous compounds and the detoxifi cation of xenobiotics in insects. Moreover, these enzymes exhibit peroxidase-like activity, therefore they may be involved in protecting organisms against the toxicity of reactive oxygen species (ROS). In the present study, we cloned a CYP4G11 gene -AccCYP4G11 -from the Chinese honey-bee (Apis cerana cerana). The open reading frame of the cDNA was 1656 bp long and encoded a 551 amino acids polypeptide, which shared high sequence identity with homologous cytochrome P450 proteins. In the genomic DNA sequence, a 5'-fl anking region consisting of 1168 bp was obtained, and some putative transcription factor binding sites were predicted. Quantitative polymerase chain reaction (Q-PCR) revealed that the level of AccCYP4G11 was higher in the epidermis than in other tissues, and Acc-CYP4G11 was expressed in all stages with the highest level in two-week-old adult worker honey-bees. More over, the expression patterns under oxidative stress indicated that Acc-CYP4G11 transcription was signifi cantly infl uenced by external factors, such as temperature challenges, ultraviolet (UV) light, and insecticide treatment. AccCYP4G11 was regulated differentially in response to oxidative stress and may be involved in protecting honey-bees from oxidative injury.
Global climate changes have led to frequent and recurrent heat stress, which has seriously affected the world maize production. The experiment presented in this paper was carried out during the maize‐growing season in 2021 and 2022 at the Huang–Huai–Hai Region Maize Science and Technology Innovation Center (36°09′N, 117°09′E) in Tai'an, Shandong province, China. The test site is located in the semi‐humid warm temperate continental monsoon climate zone, soil is brown loam. We selected different heat‐sensitive maize varieties: heat‐tolerant variety Zhengdan 958 (ZD958) and heat‐sensitive variety Xianyu335 (XY335) to study the stress effects of high temperature on the development of tassel in the key stage of its differentiation (the 12‐leaf stage, V12). We found that exposure to heat stress during the V12 stage significantly reduced the tassel size and the anther dehiscence area, making it difficult to disperse pollen, thus effectively reducing pollen production. In addition, heat stress had significant negative effects on pollen development, resulting in deformed pollen and lower pollen viability and germination rate. Our results also showed that heat stress significantly increased the activities of key reactive oxygen species‐scavenging enzymes including superoxide dismutase, peroxidase and catalase, and that the malondialdehyde and H2O2 content in tassels exposed to heat stress were significantly higher than those control group, where it should be noted that for the XY335, these effects were more pronounced than for the ZD958. The endogenous hormone content of tassels exhibited a variety of responses. After heat stress, the zeatin and salicylic acid content in tassels of both maize varieties were significantly lower than those in the respective control groups, while the abscisic acid and gibberellin acid content were significantly higher. With respect to the jasmonic acid and 3‐indoleacetic acid content, the two maize varieties exhibited opposite responses: in tassels from ZD958 plants subjected to heat stress were higher than those in the respective control group, while in tassels from XY335 plants, they were lower. The observed changes in protective enzyme activities and endogenous hormone contents induced by heat stress significantly affected the development of maize tassels and significantly reduced the amount, activity and germination rate of pollen.
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