Characterization of the S-RNase promoters from sweet cherry (Prunus avium L.)
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- Ishizaka Takako
- JST, Regional Joint Research Project of Yamagata Prefecture
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- Nakano Hideaki
- Yamagata Prefecture Agricultural Experiment Station
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- Suzuki Takashi
- Faculty of Education, Yamagata University
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- Kitashiba Hiroyasu
- JST, Regional Joint Research Project of Yamagata Prefecture
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抄録
Genomic DNA fragments containing the S3-, S4-, and S6-RNase genes were isolated from the sweet cherry (Prunus avium L.) and sequenced. Comparison of the 5'-flanking sequences of these three S-RNases indicated that a highly conserved region (designated CR) existed just upstream from the putative TATA boxes. We postulate that CR contains cis-regulatory element(s) involved in pistil expression. To examine the activity of the isolated S-RNase promoters of sweet cherry in the pistil, we transiently introduced approximately 650-bp fragments of the S4- and S6-RNase promoters fused to β-glucuronidase (GUS) gene into the pistil of the petunia using a particle bombardment technique. Histochemical analysis showed that the 5'-flanking region of each S-RNase was active in the pistil. This suggests that cis-regulatory element(s) for pistil-specific expression may exist(s) within the 650-bp region upstream from the TATA box in the sweet cherry S-RNase promoter.<br>
収録刊行物
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- Genes & Genetic Systems
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Genes & Genetic Systems 78 (2), 191-194, 2003
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詳細情報 詳細情報について
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- CRID
- 1390282680449695232
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- NII論文ID
- 130000060774
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- NII書誌ID
- AA11077421
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- COI
- 1:CAS:528:DC%2BD3sXmtVClurg%3D
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- ISSN
- 18805779
- 13417568
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- NDL書誌ID
- 6536950
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- PubMed
- 12773819
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可