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Original

Cloning And Characterization Of A Bamboo Leafy Hull Sterile1 Homologous Gene

Full Length Research Paper

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Pages 143-151 | Received 04 Oct 2005, Published online: 11 Jul 2009
 

Abstract

A cDNA named DlMADS8 was isolated from the young spikelets of the sweet bamboo, Dendrocalamus latiflorus by rapid amplification of cDNA end (RACE). DNA sequence analysis showed that DlMADS8 was composed of full ORF and 3′UTR, but without 5′UTR. The cDNA contained 1059 nucleotides and encoded a putative protein of 244 amino acid residues. The gene displayed the structure of a typical plant MADS-box gene, which consisted of a MADS domain, K domain, a short I region, and the C-terminal region. Phylogenetic analysis of plant MADS-box genes based on amino acid sequences revealed that DlMADS8 was grouped into the AGAMOUS-LIKE 2 (AGL2)-like subfamily. It was homologous to the LEAFY HULL STERILE1 (LHS1) genes of grasses. To study the functions of it, DlMADS8 cDNA clone driven by the CaMV 35S promoter was transformed into Arabidopsis thaliana. Transgenic plants of DlMADS8 exhibited the phenotypes of curled leaves and early flowering. After bolting, three novel phenotypes related to inflorescence development were observed in different transgenic plants. No obvious homeotic conversions of floral organs were observed in all of the 35S::DlMADS8 transgenic Arabidopsis plants. These results indicated that DlMADS8 probably plays a role in floral meristem determinacy and is involved in controlling the flowering time of D. latiflorus.

Acknowledgements

We thank Prof. Guangchu Zhang (Guangdong Forest Research Institute) for presenting the in vitro flowering cultures. This work was supported by National Natural Science Foundation of China (Grant No: 30200015), Natural Science Foundation of Yunnan Province (Grant No: 2002C0056M) and the Ministry of Science and Technology of China (Grant No: 2004DKA30430).

Notes

Tel: 86 871 5223018. Fax: 86 871 5217791. [email protected].

Tel: 86 871 5223504. Fax: 86 871 5217791. [email protected].

Tel: 86 871 5223504. Fax: 86 871 5217791. [email protected].

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