Sequence and Functional Analysis of the Intergenic Regions Separating Babesial Rhoptry-Associated Protein-1 (rap-1)Genes
Suarez, C. E., Palmer, G. H., Hötzel, I., Hines, S. A., and McElwain, T. F. 1998. Sequence and functional analysis of the intergenic regions separating babesial rhoptry-associated protein-1 (rap-1) genes.Experimental Parasitology90, 189–194. The rhoptry-associated protein 1 (RAP-1) expressed by all...
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Published in | Experimental parasitology Vol. 90; no. 2; pp. 189 - 194 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
01.10.1998
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Suarez, C. E., Palmer, G. H., Hötzel, I., Hines, S. A., and McElwain, T. F. 1998. Sequence and functional analysis of the intergenic regions separating babesial rhoptry-associated protein-1 (rap-1) genes.Experimental Parasitology90, 189–194. The rhoptry-associated protein 1 (RAP-1) expressed by all babesial parasites is encoded by tandemly arranged genes separated by discrete intergenic (IG) regions. We hypothesize that these IG regions regulaterap-1gene expression. InBabesia bovistwo identicalrap-1gene copies are separated by a 1.0-kb noncoding region which is also exactly conserved 5′ to therap-1gene 1. In contrast, the complexB. bigemina rap-1locus contains at least 5 polymorphicrap-1agenes separated by uncharacterized 3.38-kb regions. A genomic clone encoding the 3′ sequence ofrap-1gene copy 1, the 1 kb IG region, and the 5′ sequence of gene copy 2 was obtained by PCR amplification of DNA from the Mo7 biological clone ofB. bovisand sequenced. This was follow by amplification and sequence analysis of the 3.38-kb region separating twoB. bigemina rap-1agenes, revealing the presence of two different IG regions denominated IG-1 (0.7 kb) and IG-2 (1.3 kb), flanking a newly identifiedrap-1borf. Sequence analysis and comparison among babesialrap-1IG regions fromB. bovis, B. bigemina, B. canis, andB. ovisrevealed conservation of at least three putative regulatory boxes consistently positioned 5′ of the start of therap-1orfs. To determine whetherrap-1IG regions contained a functional promoter, the entire 1-kb IG region fromB. boviswas cloned into pCAT, a promoterless plasmid containing thecatgene. The IG region in the 5′ → 3′ orientation strongly promoted transcriptionin vitroby homologousB. bovisRNA polymerases. The presence of conserved regions 5′ to eachrap-1gene copy and among other babesialrap-1IG regions and thein vitropromoter function in the 5′ → 3′ orientation support a role for the IG region inrap-1gene regulation. |
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Bibliography: | 1997081969 L72 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0014-4894 1090-2449 |
DOI: | 10.1006/expr.1998.4321 |