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Isolation and Expression of a Novel Alligator Gene Belonging to the Sox Gene Family

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Abstract

Sox genes share a highly conserved DNA-binding motif, the HMG (high mobility group)-box domain, and have diverse roles in vertebrate embryonic development. A novel SRY-related cDNA (temporarily called Sox33) isolated from the Chinese alligator (Alligator sinensis) is 1,819 bp in length, with an open reading frame from 220 to 1113 bp, encoding a protein of 298 amino acids. Two putative polyadenylation signal sequences (AATAAA) are present upstream of the poly(A) tail in the 3′ UTR (at 1255–1260 and 1774–1779). The putative protein contains an HMG-box domain most closely related to hSox12, mSox4, rtSox11, and mSox11 homologs, indicating that alligator Sox33 belongs to group C in the Sox gene family. Alligator adult and developing tissues were tested for Sox33 mRNA by independent Northern blots using a 336-bp probe (at 907–1243) between the HMG-box and the poly(A) site I and a 277-bp probe (at 1477–1754) between the two polyadenylation sites. Two transcripts (1.3 kb and 1.8 kb) in developing brain and one (1.8 kb) in adult brain were identified by the 336-bp probe; only one transcript (1.8 kb) in developing and adult brains was detected by the 277-bp probe. The results suggest that alligator Sox33 may use a different polyadenylation mechanism in the developing brain and play a role in the development and maintenance of the nervous system.

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Acknowledgments

We would like to acknowledge the staff of the Research Center for Chinese Alligator Reproduction in China for providing the experimental material, and the staff of Shanghai Biolink Informatics Inc. for expert technical assistance. This work was supported by the Natural Science Foundation of Hunan Province (Grant No. 04JJ40021) and the Scientific Research Foundation for Doctor in Nanhua University (Grant No. 5-03-XJQ-03-044).

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Correspondence to Jifang Zheng.

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Zheng, J., Hu, N., Zhu, M. et al. Isolation and Expression of a Novel Alligator Gene Belonging to the Sox Gene Family. Biochem Genet 47, 137–146 (2009). https://doi.org/10.1007/s10528-008-9213-3

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  • DOI: https://doi.org/10.1007/s10528-008-9213-3

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