Elsevier

Gene Expression Patterns

Volume 11, Issues 1–2, January–February 2011, Pages 3-11
Gene Expression Patterns

The HMGB protein gene family in zebrafish: Evolution and embryonic expression patterns

https://doi.org/10.1016/j.gep.2010.08.006Get rights and content

Abstract

The High-Mobility Group Box (HMGB) proteins are highly abundant proteins with both nuclear and extracellular roles in key biological processes. In mammals, three family members are present: HMGB1, HMGB2 and HMGB3. We characterized the HMGB family in zebrafish and report a detailed phylogenetic analysis of HMGB proteins. The B1, B2, and B3 subfamilies are present in cartilaginous fish, bony fish, and tetrapods, while jawless fish sequences emerge as basal to the gene family expansion. Two co-orthologs of each mammalian HMGB gene are present in zebrafish. All six zebrafish hmgb genes are maternally expressed, but huge differences in expression levels exist during embryonic development. The hmgb2a/hmgb2b genes are the most highly expressed, while hmgb3b is expressed at the lowest level. Remarkably, hmgb3 genes are not present in fugu, medaka, Tetraodon and stickleback. Our analysis highlights substantial overlaps, but also subtle differences and specificities in the expression patterns of the zebrafish hmgb genes.

Section snippets

Results and discussion

The High-Mobility Group Box (HMGB) proteins are abundant non-histone chromatin components implicated in major DNA transactions, such as transcription, recombination, and repair (Bianchi and Agresti, 2005, Bustin, 2001, Lange and Vasquez, 2009). HMGB proteins are highly mobile nuclear proteins that dynamically bind DNA and nucleoprotein complexes through their HMG boxes. These are L-shaped basic domains, that contact DNA through the minor groove and induce sharp DNA bending. HMGB1, the first

Zebrafish husbandry

Zebrafish of the wild-type AB line (obtained from Wilson lab, University College London) were raised and maintained according to established techniques (Westerfield, 1993). Embryos used in whole-mount in situ hybridization were raised in 0.003% PTU (Sigma) to prevent pigmentation.

Identification and analysis of hmgb sequences

Zebrafish hmgb sequences were identified using mouse HMGB1, HMGB2, and HMGB3 protein sequences to query Danio rerio nucleotide collection/EST databases with the TBLASTN program. A predicted gene, identical to the zf

Acknowledgments

We would like to thank C. Lora-Lamia for advice on histological techniques, G. Brunetti for his help in fish husbandry. We also thank Sylvie Rétaux for sharing with us lamprey sequences before publication in databases, Matthieu Muffato and Hugues Roest Crollius for help with synteny analysis, Gavin Laird for discussions on zebrafish genome annotation. We acknowledge financial support from Italian Ministry of Education, University, and Research (MIUR-Cofin 2004 to M.B.), Fondazione Cariplo

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    Present address: Division of Clinical Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.

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