中国农业科学 ›› 2018, Vol. 51 ›› Issue (10): 1830-1841.doi: 10.3864/j.issn.0578-1752.2018.10.002

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

过表达谷子SiANT1对水稻耐盐性的影响

宁蕾1(), 王曙光1, 琚鹏举1, 柏星轩1, 葛林豪2, 齐欣2, 姜奇彦2, 孙现军2, 陈明2(), 孙黛珍1()   

  1. 1山西农业大学农学院,山西太谷 030800
    2中国农业科学院作物科学研究所,北京 100081
  • 收稿日期:2017-12-01 接受日期:2018-02-02 出版日期:2018-05-16 发布日期:2018-05-16
  • 联系方式: 联系方式:宁蕾,E-mail:ninglei02@163.com。
  • 基金资助:
    国家转基因生物新品种培育科技重大专项(2016ZX08002005)、谷子氮素高效利用重要基因克隆及育种价值评估(2018ZX0800924B)

Rice Overexpression of Millet SiANT1 Gene Increases Salt Tolerance

Lei NING1(), ShuGuang WANG1, PengJu JU1, XingXuan BAI1, LinHao GE2, Xin QI2, QiYan JIANG2, XianJun SUN2, Ming CHEN2(), DaiZhen SUN1()   

  1. 1College of Agronomy, Shanxi Agricultural University, Taigu 030800, Shanxi
    2Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081
  • Received:2017-12-01 Accepted:2018-02-02 Published:2018-05-16 Online:2018-05-16

摘要:

目的 高盐胁迫是影响作物产量的主要因素之一,谷子(Setaria italica L.)具有耐逆性强的特点,从谷子中筛选耐盐基因对于利用基因工程的手段培育耐盐作物新品种具有重要意义。方法 分析谷子AP2/ERF类转录因子类基因SiANT1在豫谷一号幼苗期在高盐、低氮、PEG模拟干旱处理条件下的表达模式;进而利用农杆菌转化法将SiANT1转入模式作物水稻品种Kitaake;分别用0.9% 盐水和自来水浸泡过表达SiANT1水稻和野生型Kitaake的种子,观察其萌芽期的表型并统计发芽率;用含0.9% NaCl的Hogland营养液室内处理水稻幼苗10 d,65℃烘48 h之后称量干重;同时将其种植在大田,在水稻孕穗前用0.9%盐水灌溉一次,统计成熟后过表达SiANT1水稻各株系和野生型的单株籽粒重、株高、单株分蘖数,对其耐盐性进行评价;利用定量Real time-PCR方法,验证分析转基因水稻株系中SiANT1及其可能的下游基因的相对表达情况。结果 谷子SiANT1蛋白(XP004985124.1,SiANT1)属于AP2亚族,与高粱(XP021318293.1,SbANT1)和玉米(XP008658933.1,ZmAP2)亲缘关系较近;豫谷一号中SiANT1的表达受高盐胁迫(100 mmol·L-1 NaCl)诱导;将SiANT1和LP047 1118-Bar-ubi-EDLL载体连接,利用农杆菌转化法将SiANT1转入到水稻基因组中,筛选得阳性T0植株,繁殖两代得T3代种子;自来水浸泡下,过表达SiANT1水稻种子萌发率和野生型相差不大,萌芽率为90%以上;0.9%盐水浸泡下,过表达SiANT1水稻种子萌发明显受到抑制,与野生型相比,过表达SiANT1水稻种子露白推迟,但最终(处理120 h)萌芽率达到80%以上;室内水稻苗期用0.9% NaCl处理后,过表达SiANT1水稻的单株干重较受体Kitaake增重14.11%—37.42%,在1%水平上呈显著差异;大田水稻成熟后过表达SiANT1株系单株籽粒重较受体Kitaake增产56.12%—76.58%,在5%水平上呈显著差异,单株分蘖数增多、株高增加,但与野生型无显著差异;半定量RT-PCR分析表明,过表达SiANT1的3个水稻株系都在RNA水平上表达SiANT1;定量Real time-PCR结果表明,过表达SiANT1的3个水稻株系间SiANT1的相对表达量有所差异,但较受体而言,都极显著增加,并且其内源耐盐相关基因OsSOS1OsZFP182的相对表达量分别较受体提高1.1—1.7倍和1.6—2.3倍。结论 OsSOS1OsZFP182是耐盐相关基因已被证实,SiANT1具有一定的耐盐性,过表达SiANT1水稻可能是通过增加下游基因OsSOS1OsZFP182的表达从而提高耐盐性。

关键词: 谷子, SiANT1, AP2/ERF类转录因子, 耐盐性, 耐盐胁迫相关基因

Abstract:

【Objective】 High salt stress is one of the main factors affecting crop yield. Setaria italica L. is characterized by its strong tolerance to stress. Therefore, screening salt tolerant related genes from millet is important for salt stress tolerant improvement of crops through genetic transformation.【Method】 The expression profile of AP2/ERF like gene SiANT1 were analyzed in Yugu 1 at seedling stage under high salt, low nitrogen and PEG simulated drought conditions. Millet gene SiANT1 was transformed into rice Kitaake by agrobacterium-mediated transformation method. overexpressing SiANT1 rice seeds and wild type Kitaake were digested with 0.9% saline and tap water, respectively. The phenotypes of germinating stage and germination rate were observed. Rice seedlings were treated with 0.9% NaCl in Hogland nutrient solution for 10 days and then dried at 65℃ for 48 hours dry weights of all the rice overexpressing SiANT1 and wild type (WT) plants were analyzed. At the same time, phenotype of all plants was analyzed in the field and all plants were irrigated once with 0.9% saline before rice pregnancy. Under the similar salt treatment condition, single seed grain weigh plant height and tiller number per plant of the overexpressing SiANT1 rice lines and wild type were also analyzed. The real time-PCR method was used to verify the expression of SiANT1 and its possible downstream genes in transgenic rice lines.【Result】 Setaria italica L. SiANT1 protein (XP004985124.1, SiANT1) belongs to the AP2 subfamily and has a close genetic relationship with sorghum (XP021318293.1, SbANT1) and maize (XP008658933.1, ZmAP2).The gene of SiANT1 was induced by high salt stress (100 mmol·L-1 NaCl) in Yugu 1. The SiANT1 was ligated to LP047 1118-Bar-ubi-EDLL vector, Agrobacterium transformation method was used to transfer SiANT1 into rice genome, positive T0 plants were screened, then breeded two generations and got T3 seeds. Under water immersion, the germination rate of SiANT1 overexpression rice was similar to that of wild type. Germination rate was more than 90%. Under 0.9% saline immersion, the overexpression of SiANT1 was significantly inhibited. Compared with the wild type, over-expression of SiANT1 rice seeds dew white was delayed, but finally(treatmented for 120h) germination rate was more than 80% .After treatment with 0.9% NaCl at seedling stage in greenhouse, the dry weight of single plant overexpressing SiANT1 increased 14.11%-37.42% more than that of WT, which had significant difference at the 1% level. The grain weight of transgenic rice overexpression SiANT1 in field increased 56.12%-76.58% higher than that of WT, which had significant difference at the 5% level, the number of tillers per plant and plant height increased, but there was no significant difference with the wild-type. Semi-quantitative RT-PCR analysis showed that all three rice lines overexpressing SiANT1 expressed SiANT1 at the RNA level. Real time-PCR results showed that the relative expression level of SiANT1 in three rice lines overexpressing SiANT1 was different but significantly increased compared with that of the recipient, and the relative expression levels of endogenous salt-tolerance-related genes OsSOS1 and OsZFP182 were 1.1-1.7 fold and 1.6-2.3 fold respectively higher than that of the recipient.【Conclusion】 It has been confirmed that OsSOS1 and OsZFP182 are salt tolerance related genes. SiANT1 gene has certain salt tolerance. Overexpression of SiANT1 in rice may increase salt tolerance by increasing the expression of downstream genes OsSOS1 and OsZFP182.

Key words: millet (Setaria italica L.), SiANT1 gene, AP2 / ERF transcription factor, salt tolerance, salt tolerant related genes