JP2008535489A5 - - Google Patents

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JP2008535489A5
JP2008535489A5 JP2008504705A JP2008504705A JP2008535489A5 JP 2008535489 A5 JP2008535489 A5 JP 2008535489A5 JP 2008504705 A JP2008504705 A JP 2008504705A JP 2008504705 A JP2008504705 A JP 2008504705A JP 2008535489 A5 JP2008535489 A5 JP 2008535489A5
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  1. 生物サンプル中のエリートイベントA2704−12を同定するための方法であって、A2704−12の5’または3’の隣接領域を特異的に認識する特異的プライマーまたはプローブで、A2704−12の特異的領域を検出することを含む方法。
  2. 請求項1記載の方法であって、
    前記方法が、少なくとも二つのプライマーとのポリメラーゼ連鎖反応を利用して、前記生物サンプル中に存在する核酸から、100〜500bpの間のDNAフラグメントを増幅することを含み、
    前記プライマーのうちの一つが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列を有するA2704−12の5’隣接領域、または配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列を有するA2704−12の3’隣接領域を認識し、
    前記プライマーの他のプライマーが、配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列を有する外来DNA中の配列を認識する、
    方法。
  3. 請求項2記載の方法であって、
    5’隣接領域を認識する前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列からなるか、またはA2704−12の3’隣接領域を認識する前記プライマーが、配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列からなり、かつ
    外来DNA中の配列を認識する前記プライマーが、配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列から選択される17〜200の連続的ヌクレオチドで構成されている、
    方法。
  4. 請求項2記載の方法であって、
    5’隣接領域を認識する前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列をその極端の3’末端に含んでいるか、あるいはA2704−12の3’隣接領域を認識する前記プライマーが、配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列をその極端の3’末端に含んでおり、かつ
    外来DNA中の配列を認識する前記プライマーが、配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドをその3’末端に含んでいる、
    方法。
  5. 前記プライマーがそれぞれ配列番号4と配列番号8の配列を含んでいる、請求項4記載の方法。
  6. A2704−12同定プロトコルを使用して、約185bpのフラグメントを増幅することを含む、請求項5記載の方法。
  7. 生物サンプル中のエリートイベントA2704−12を同定するためのキットであって、
    配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列を有する、A2704−12の5’隣接領域を認識する一つのプライマー、または配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列を有する、A2704−12の3’隣接領域を認識する一つのプライマー、および
    配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列を有する前記外来DNA中の配列を認識する一つのプライマーを含む、
    キット。
  8. 請求項7記載のキットであって、
    5’隣接領域を認識する前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列からなるか、あるいはA2704−12の3’隣接領域を認識する前記プライマーが、配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列からなり、かつ
    外来DNA中の配列を認識する前記プライマーが、配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドからなる、
    キット。
  9. 請求項7記載のキットにおいて、
    5’隣接領域を認識する前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列をその極端の3’末端に含んでいるか、あるいはA2704−12の3’隣接領域を認識する前記プライマーが、配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列をその極端の3’末端に含んでおり、かつ
    外来DNA中の配列を認識する前記プライマーが、配列番号1、ヌクレオチド210〜ヌクレオチド720の相補体のヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドをその3’末端に含んでいる、
    キット。
  10. 配列番号4の配列からなるプライマーと、配列番号8の配列からなるプライマーとを含む、請求項7記載のキット。
  11. A2704−12の5’または3’隣接領域中の配列を最適化したPCR条件下で、特異的に認識する配列を有する、A2704−12 PCR同定プロトコルで使用するためのプライマーであって、
    前記5’隣接領域が、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列を有し、かつ前記3’隣接領域が、配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列を有する、
    プライマー。
  12. 前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された17〜200の連続的ヌクレオチドのヌクレオチド配列からなる、請求項11記載のプライマー。
  13. 前記プライマーが、配列番号1、ヌクレオチド1〜ヌクレオチド209のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列、または配列番号2、ヌクレオチド569〜ヌクレオチド1000の相補体のヌクレオチド配列から選択された少なくとも17の連続的ヌクレオチドのヌクレオチド配列をその極端の3’末端に含んでいる、請求項11記載のプライマー。
  14. 配列番号4の配列をその極端の3’末端に含むプライマー。
  15. 配列番号8の配列をその極端の3’末端に含むプライマー。
  16. A2704−12に対し特異的なプローブを使用して、生物サンプルの核酸をハイブリダイズすることを含む、請求項1記載の方法。
  17. 前記特異的プローブの配列が、A2704−12の5’隣接配列または3’隣接配列の部分、およびそれに隣接している外来DNAの配列を含む配列と、少なくとも80%の配列同一性を有する、請求項16の方法。
  18. 前記特異的プローブの配列が、配列番号1、ヌクレオチド160〜260、または配列番号2、ヌクレオチド520〜620、または前記配列の相補体と、少なくとも80%の配列同一性を有する、請求項17記載の方法。
  19. 生物サンプル中のエリートイベントA2704−12を同定するためのキットであって、A2704−12の特異的領域に特異的にハイブリダイズできる特異的プローブを含む、キット。
  20. A2704−12の5’隣接配列または3’隣接配列の部分、およびそれに隣接している外来DNAの配列を含む配列と、前記特異的プローブの配列が少なくとも80%の配列同一性を有する、請求項19記載のキット。
  21. 前記特異的プローブの配列が、配列番号1、ヌクレオチド160〜260、または配列番号2、ヌクレオチド520〜620、または前記配列の相補体と少なくとも80%の配列同一性を有する、請求項20記載のキット。
  22. 生物サンプル中のエリートイベントA2704−12を同定するための特異的プローブ。
  23. A2704−12の5’隣接配列または3’隣接配列の部分、およびそれに隣接している外来DNAの配列を含む配列、またはその相補体と、少なくとも80%の配列同一性を有する、請求項22記載のプローブ。
  24. 配列番号1、ヌクレオチド160〜260、または配列番号2、ヌクレオチド520〜620、または前記配列の相補体と少なくとも80%の配列同一性を有する、請求項23記載のプローブ。
  25. 配列が、配列番号1、ヌクレオチド160〜260、または配列番号2、ヌクレオチド520〜620、または前記配列の相補体に本質的に類似している、生物サンプル中のエリートイベントA2704−12を同定するための特異的プローブ。
  26. 種子サンプルにおいて、A2704−12の5’または3’隣接領域を特異的に認識する特異的プライマーまたはプローブでA2704−12の特異的領域を検出することを含む、種子純度を確認する方法。
  27. 種子ロットのサンプルにおいて、A2704−12の5’または3’隣接領域を特異的に認識する特異的プライマーまたはプローブでA2704−12の特異的領域を検出することを含む、A2704−12の存在を確認するため種子をスクリーニングする方法。
  28. ゲノム中にエリートイベントA2704−12を含む、ダイズ植物体、または細胞、部分、種子またはその子孫。
JP2008504705A 2005-04-08 2006-04-04 エリートイベントa2704−12、ならびに生物サンプル中の該イベントを同定するための方法およびキット Active JP5256020B2 (ja)

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EP05075833 2005-04-08
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US67021305P 2005-04-11 2005-04-11
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PCT/EP2006/003454 WO2006108674A2 (en) 2005-04-08 2006-04-04 Elite event a2704-12 and methods and kits for identifying such event in biological samples

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