Cloning and analysis of the flowering-related gene，<em>BoAP</em>3，in <em>Bambusa oldhamii</em>

ZHU Longfei; XU Yingwu; LIN Xinchun

doi:10.11833/j.issn.2095-0756.2013.06.006

Volume 30 Issue 6

Nov. 2013

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ZHU Longfei, XU Yingwu, LIN Xinchun. Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii[J]. Journal of Zhejiang A&F University, 2013, 30(6): 839-843. doi: 10.11833/j.issn.2095-0756.2013.06.006

Citation:

ZHU Longfei, XU Yingwu, LIN Xinchun. Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii[J]. Journal of Zhejiang A&F University, 2013, 30(6): 839-843. doi: 10.11833/j.issn.2095-0756.2013.06.006

Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

doi: 10.11833/j.issn.2095-0756.2013.06.006

1.
The Nurturing Station for the State Key Laboratory of Subtropical Silviculture，Zhejiang A & F University，Lin’an 311300，Zhejiang，China

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Corresponding author: LIN Xinchun
Received Date: 2012-11-21
Rev Recd Date: 2013-01-07
Publish Date: 2013-12-20

Abstract

MADS-box family genes play important roles in the determination of floral meristem identity and the development of floral organ identity. Here we reported a full length MADS-box gene obtained from the flower bud of Bambusa oldhamii. It was named as BoAP3 based on sequence similarity. DNA sequence analysis showed that the BoAP3 was 654 bp length and contained an open reading flame（ORF） encoding a protein of 218 mino acids that shared over 80% homology with Oryza sativa and Triticum aestivum of APETALA3 homologues. The protein showed a typical MADS-box gene structure containing MADS domain，K domain，I region and C terminus. Quantitative real-time PCR analysis revealed that the expression level of BoAP3 in flower buds was 8.1 times higher than in vegetative shoots，suggested that BoAP3 may be involved in floral organ development. ［Ch，4 fig. 14 ref.］
- forest tree breeding,
- Bambusa oldhamii,
- BoAP3,
- MADS-box

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通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

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Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

1. The Nurturing Station for the State Key Laboratory of Subtropical Silviculture，Zhejiang A & F University，Lin’an 311300，Zhejiang，China

Corresponding author: LIN Xinchun

Received Date: 2012-11-21

Rev Recd Date: 2013-01-07

Publish Date: 2013-12-20

Key words:

Abstract: MADS-box family genes play important roles in the determination of floral meristem identity and the development of floral organ identity. Here we reported a full length MADS-box gene obtained from the flower bud of Bambusa oldhamii. It was named as BoAP3 based on sequence similarity. DNA sequence analysis showed that the BoAP3 was 654 bp length and contained an open reading flame（ORF） encoding a protein of 218 mino acids that shared over 80% homology with Oryza sativa and Triticum aestivum of APETALA3 homologues. The protein showed a typical MADS-box gene structure containing MADS domain，K domain，I region and C terminus. Quantitative real-time PCR analysis revealed that the expression level of BoAP3 in flower buds was 8.1 times higher than in vegetative shoots，suggested that BoAP3 may be involved in floral organ development. ［Ch，4 fig. 14 ref.］

Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

doi: 10.11833/j.issn.2095-0756.2013.06.006

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通讯作者: 陈斌, bchen63@163.com

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Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

doi: 10.11833/j.issn.2095-0756.2013.06.006

1. The Nurturing Station for the State Key Laboratory of Subtropical Silviculture，Zhejiang A & F University，Lin’an 311300，Zhejiang，China

Corresponding author: LIN Xinchun

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Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

doi: 10.11833/j.issn.2095-0756.2013.06.006

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通讯作者: 陈斌, bchen63@163.com

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Cloning and analysis of the flowering-related gene，BoAP3，in Bambusa oldhamii

doi: 10.11833/j.issn.2095-0756.2013.06.006

1. The Nurturing Station for the State Key Laboratory of Subtropical Silviculture，Zhejiang A & F University，Lin’an 311300，Zhejiang，China

Corresponding author: LIN Xinchun

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