您的位置: 专家智库 > >

李军

作品数:3 被引量:10H指数:2
供职机构:中国科学院遗传与发育生物学研究所更多>>
发文基金:国家重点基础研究发展计划国家高技术研究发展计划更多>>
相关领域:农业科学生物学更多>>

文献类型

  • 3篇中文期刊文章

领域

  • 3篇农业科学
  • 1篇生物学

主题

  • 2篇水稻
  • 1篇英文
  • 1篇育性
  • 1篇育性转换
  • 1篇水稻不育系
  • 1篇温敏不育系
  • 1篇基因
  • 1篇基因组
  • 1篇基因组DNA
  • 1篇安农
  • 1篇安农S-1
  • 1篇TGMS
  • 1篇APRT
  • 1篇CLONIN...
  • 1篇GENE
  • 1篇不育
  • 1篇不育系
  • 1篇测序
  • 1篇纯化
  • 1篇RICE

机构

  • 3篇中国科学院遗...
  • 1篇山东大学
  • 1篇山东农业大学
  • 1篇湖南杂交水稻...
  • 1篇青岛农业大学
  • 1篇中国科学院

作者

  • 3篇李军
  • 3篇王斌
  • 2篇梁春阳
  • 2篇杨继良
  • 1篇金德敏
  • 1篇邓启云
  • 1篇王庆华
  • 1篇邢全华
  • 1篇杨典洱
  • 1篇刘斌
  • 1篇束静
  • 1篇郭宝太
  • 1篇王辉
  • 1篇翁曼丽
  • 1篇邓启云

传媒

  • 1篇Acta B...
  • 1篇生物化学与生...
  • 1篇Journa...

年份

  • 1篇2004
  • 2篇2003
3 条 记 录,以下是 1-3
排序方式:
Cloning of the APRT Gene from Rice and Analysis of Its Association with TGMS被引量:4
2003年
Adenine phosphoribosyltransferase (APRT) is the major enzyme that converts adenine into adenosine-3'-phosphate (AMP). APRT-deficient mutant caused by APRT gene mutation results in the male sterility in Arabidopsis thaliana L. In order to confirm the existence of rice APRT gene and to investigate its association with thermo-sensitive genic male sterile (TGMS) phenotype of rice, a APRT gene was identified from BLAST search of the rice genome database using APRT gene sequences from other plant species as probes. Further, the gene was cloned from rice and named APRT(GenBank accession number AY238894) using the combination of bioinformatic and experimental approaches. The rice APRT was located in the 56 000 bp to 63 000 bp region of a rice bacterial artificial chromosome (BAC) clone (AL606604) on chromosome 4 and was deduced by software from the positive DNA clone. Its cDNA was amplified by reverse transcriptase-polymerase chain reaction (RT-PCR) using primers designed according to the sequence of the putative gene. The full-length cDNA was obtained by rapid amplification of cDNA ends (RACE) procedure and was sequenced. Open reading frame (ORF) analysis indicated that the rice APRT gene encodes a peptide of 212 amino acid residues, including seven exons and six introns. Using reverse position specific BLAST (RPS-BLAST), the APRT domain was identified in the polypeptide. The homology comparison demonstrated that the polypeptide exhibits 54.9%, 54.9%, 49.6% and 59.5% identity with that from Hordeum vulgare, Ttriticum aestivum, and A. thaliana (APRT types 1 and 2), respectively. Comparing the sequence of APRT gene from TGMS mutant lines 'Annong S-1' (Oryza sativa subsp. indica) with that from its corresponding wild type 'Annong F' (Oryza sativa. subsp. indica), we found that there are five single nucleotid polymorphism (SNP) sites in the gene of 'Annong S-1', which locate mainly in the second intron. However, the result of cDNA sequencing showed that these SNP sites do not damage the successful splicing of intron 2. Qual
李军梁春阳杨继良邢全华杨典洱邓启云翁曼丽王斌
关键词:APRTRICE
水稻不育系安农S-1育性转换及相关基因的表达分析被引量:6
2004年
通过在自然环境和高温温室内对安农S 1的不同部位进行高温、低温诱导处理 ,对水稻温敏核不育系安农S 1的温度敏感时期和诱导部位进行了研究。总共进行了 8种处理 ,结果表明 :安农S 1的育性转换时期是从花粉母细胞形成到减数分裂的四分体时期之前。在育性转换时期 ,处于高温的条件下 ,根部低温处理不能诱导安农S 1可育 ,穗部低温处理可以使安农S 1保持可育 ,可见安农S 1的温度敏感部位在幼穗。aprt基因和育性相关 ,用RT PCR方法研究了aprt基因在安农S 1不同部位和不同温度环境的表达变化 ,结果显示 ,在幼穗中aprt基因的表达在高温环境中被大幅度下调 ,而在叶中和根中的变化比较小 ,这说明幼穗对温度最敏感 ,从侧面验证了引起安农S 1育性转换的温度敏感部位是在幼穗。
梁春阳李军束静邓启云邓启云郭宝太
关键词:水稻安农S-1温敏不育系
Shotgun法测序制备高纯度水稻基因组DNA的方法探讨(英文)
2003年
在用散弹 (shotgun)法测定水稻 (OryzasativaL .ssp .indica)基因组全序列的过程中 ,叶绿体和线粒体DNA的污染问题非常严峻 .应用脉冲场电泳 (PFGE)技术对水稻基因组DNA进行纯化 ,结果表明它能够有效去除叶绿体和线粒体DNA ,使其污染率从 3%降低到 0 2 % .同时 ,比较了水稻绿苗和黄化苗的DNA得率 ,以及HB法和NIB法制备大分子质量(HMW)DNA的异同 .最后提出一套制备水稻基因组DNA的方法 ,包括黄化苗培养 ;细胞核的分离、包埋和裂解 ;脉冲场电泳纯化、回收聚集在低熔点 (LMP)胶中的水稻HMWDNA .用该方法所得的水稻基因组DNA ,纯度高 (无叶绿体和线粒体DNA污染 )、基因组完整 (机械剪切和降解少 )、回收率高 (操作过程中DNA损失少 ) .另外 ,首次报道在融化的低熔点(LMP)胶中对水稻HMWDNA于 38℃进行超声波处理 ,能够获得用于shotgun文库和梯度文库构建所需要的各种DNA片段(1 5~ 3kb ,3~ 12kb) 。
杨继良王辉王庆华李军刘斌金德敏王斌
关键词:测序水稻基因组DNA纯化
共1页<1>
聚类工具0