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Characterisation of the human CD30 ligand gene structure.

作者信息

Croager E J, Abraham L J

机构信息

Department of Biochemistry, University of Western Australia, Nedlands.

出版信息

Biochim Biophys Acta. 1997 Sep 12;1353(3):231-5. doi: 10.1016/s0167-4781(97)00108-5.

DOI:10.1016/s0167-4781(97)00108-5
PMID:9349718
Abstract

The gene for the human CD30 ligand was molecularly cloned, sequenced and characterised. The gene structure consisted of four exons and three intervening introns spaced over 17.1 kb of genomic DNA. The 5' flanking region of the CD30L gene was sequenced and analysis of the region revealed the presence of several regulatory regions including a poly-dT element directly upstream from the transcription start site and consensus sequences for AP4, IK2, MZF1, E47 and ELK/cETS1. The absence of a canionical TATA motif suggests CD30L gene expression is regulated by a TATA-less promoter.

摘要

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