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First published online October 3, 2002; 10.1104/pp.005538

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Plant Physiol, October 2002, Vol. 130, pp. 666-674

Molecular Characterization of the Cotton GhTUB1 Gene That Is Preferentially Expressed in Fiber1

Xue-Bao Li,* Lin Cai, Ning-Hui Cheng,2 and Jian-Wei Liu3

Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore 117604

Each fiber of cotton (Gossypium hirsutum) is a single epidermal cell that rapidly elongates to 2.5 to 3.0 cm from the ovule surface within about 16 d after anthesis. A large number of genes are required for fiber differentiation and development, but so far, little is known about how these genes control and regulate the process of fiber development. To investigate gene expression patterns in fiber, a cDNA, GhTUB1, encoding beta -tubulin was isolated from a cotton fiber cDNA library. The analyses of RNA northern-blot hybridization and reverse transcriptase-polymerase chain reaction demonstrated that GhTUB1 transcripts preferentially accumulated at high levels in fiber, at low levels in ovules at the early stage of cotton boll development, and at very low levels in other tissues of cotton. The corresponding GhTUB1 gene including the promoter region was isolated by screening a cotton genomic DNA library. To demonstrate the specificity of the GhTUB1 promoter, the 5'-flanking region including the promoter and 5'-untranslated region was fused with the beta -glucuronidase reporter gene. The expression of the reporter chimera was examined in a large number of transgenic cotton plants. Histochemical assays demonstrated that GhTUB1::beta -glucuronidase fusion genes were expressed preferentially at high levels in fiber and primary root tip of 1- to 3-d-old seedlings and at low levels in other tissues such as ovule, pollen, seedling cotyledon, and root basal portion. The results suggested that the GhTUB1 gene may play a distinct and required role in fiber development. In addition, the GhTUB1 promoter may have great potential for cotton improvement by genetic engineering.


1 This work was supported by Delta and Pine Land Co. and by the National Science and Technology Board (Republic of Singapore).

2 Present address: Baylor College of Medicine, Children's Nutrition Research Center, Room 11004, 1100 Bates Street, Houston, TX 77030.

3 Present address: Syngenta Singapore Pte Ltd., 6 Temasek Boulevard, 09-02 Suntec Tower 4, Singapore 038986.

* Corresponding author; e-mail xbli{at}tll.org.sg; fax 65-6872-7007.

© 2002 American Society of Plant Physiologists



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