Developmental regulation and expression of the zebrafish connexin43 gene

被引:32
作者
Chatterjee, B
Chin, AJ
Valdimarsson, G
Finis, C
Sonntag, JM
Choi, BY
Tao, L
Balasubramanian, K
Bell, C
Krufka, A
Kozlowski, DJ
Johnson, RG
Lo, CW
机构
[1] NHLBI, Dev Biol Lab, NIH, Bethesda, MD 20814 USA
[2] Univ Penn, Sch Med, Dept Pediat, Div Cardiol, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Div Cardiol, Philadelphia, PA 19104 USA
[4] Univ Manitoba, Dept Zool, Winnipeg, MB R3T 2N2, Canada
[5] Univ Manitoba, Dept Biochem & Mol Genet, Winnipeg, MB R3T 2N2, Canada
[6] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN USA
[7] Med Coll Georgia, Dept Anat & Cellular Biol, Inst Mol Med & Genet, Augusta, GA 30912 USA
关键词
gap junction; connexin; Cx43; Cx32.2; promoter; zebrafish; mouse; embryo;
D O I
10.1002/dvdy.20426
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We cloned and sequenced the zebrafish (Danio rerio) connexin43 (Cx43 alpha 1) gone. The predicted protein sequence shows a high degree of sequence conservation. Transcript analyses revealed multiple transcription start sites and a potential alternative transcript encoding a N-terminally truncated Cx43 alpha 1 protein. Maternal Cx43a1 transcripts were detected, with zygotic expression initiated before gastrulation. In situ hybridization revealed many Cx43 alpha 1 expression domains, including the notochord and brain, heart and vasculature, many resembling patterns seen in mammalian embryos. Of interest, a reporter construct under control of the mouse Cx43 alpha 1 promoter was observed to drive green fluorescent protein expression in zebrafish embryos in domains mimicking the native Cx43 alpha 1 expression pattern in fish and mice. Sequence comparison between the mouse and zebrafish Cx43 alpha 1 promoter sequences, showed the conservation of several transcription factor motifs, which otherwise shared little overall sequence homology. The conservation of protein sequence and developmental gene regulation would suggest that Cx43 alpha 1 gap junctions are likely to have conserved roles in vertebrate embryonic development. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:890 / 906
页数:17
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