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玉米中的可移动系统 En :III. 与突变事件相关的转座。

The En mutable system in maize : III. Transposition associated with mutational events.

机构信息

Agronomy Dept., Iowa State Univ., Ames, Iowa, USA.

出版信息

Theor Appl Genet. 1970 Jan;40(8):367-77. doi: 10.1007/BF00285416.

Abstract
  1. The mutable allele, a 1 (m(pa-pu)) of the En system at the a 1 locus in maize mutates somatically and germinally to pale, colorless, and purple. 2. Colorless and pale germinal deviants arise at a high frequency. The colorless is more frequent than the pale, and each is more frequent than purple. Frequency is correlated with timing of the somatic mutation event - the earlier colorless sectoring is correlated with the higher frequency of colorless deviants. 3. The regulatory element, En, has been identified at the a 1 locus. The origin of colorless and pale deviants is accompanied by the transposition of an En element away from the a 1 site. 4. The transposing event may lead to implantation of En on the same chromosome, on another chromosome, or no implantation occurs. Transposition to a linked site occurs approximately 25% of the time. There is a preference for transposition to sites 6-20 units from a 1. 5. Secondary transpositions of En occur, and in one test, approximately 12% of the time, to an independent position. Secondary transpositions take place to new linked sites. 6. Preliminary data indicate that transpositions can occur to both distal and proximal positions on chromosome 3. 7. Since differences exist in the behaviour of elements in transposition, it is likely that the transposition event probably is dependent on the elements of specific mutable systems and differing elements within a system. 8. Theoretical aspects of diverse types of impairment of normal gene function by inserted elements is discussed.
摘要
  1. 玉米 a1 座位 En 系统的可变性等位基因 a1(m(pa-pu)),体细胞和生殖细胞发生突变,产生无色、苍白和紫色。

  2. 无色和苍白的生殖偏差发生频率较高。无色比苍白更常见,每种都比紫色更常见。频率与体细胞突变事件的时间有关——无色区域化越早,无色偏差的频率就越高。

  3. 在 a1 座位上已经鉴定出调控元件 En。无色和苍白偏差的起源伴随着 En 元件从 a1 位点的转位。

  4. 转位事件可能导致 En 植入同一染色体、另一染色体或不植入。转位到连锁位点的发生频率约为 25%。En 倾向于转位到距 a1 约 6-20 个单位的位点。

  5. 会发生 En 的二次转位,在一次测试中,约有 12%的时间发生在独立位置。二次转位发生在新的连锁位点上。

  6. 初步数据表明,转位可以发生在染色体 3 的远端和近端位置。

  7. 由于转位元件的行为存在差异,转位事件可能依赖于特定可变性系统的元件和系统内不同的元件。

  8. 讨论了插入元件对正常基因功能的多种类型损伤的理论方面。

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