首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Molecular Characterization of the D Surface Protein Gene Subfamily in Paramecium tetraurelia
Authors:MARION BREUER  GERALD SCHULTE  KLAUS J SCHWEGMANN  HELMUT J SCHMIDT
Institution:Institute for General Zoology and Genetics, University of Münster, Schloβplatz 5, 48149 Münster, Germany,;Department of Biology, University of Kaiserslautern, Building 14.2, Erwin-Schrödinger-Straβe, 67663 Kaiserslautern, Germany
Abstract:ABSTRACT. When Paramecium tetraurelia expresses the D serotype, detectable by serum tests, high molecular mRNA could be isolated, which corresponds to the molecular mass of the D surface protein. Using this D specific mRNA as a probe for screenings in different genomic libraries a subfamily of five very similar genes was found, named α-51D, γ1-51D, γ2-51D, δ-51D and ε-51D. Each of them is about 8-kb long, they show regions of identity to each other, and there is no evidence that any are defective genes or pseudogenes. Up to now serotype D is the only known serotype showing this phenomenon. Another novel feature is that two of the D isogenes are closely linked. The sequence for the entire coding region of the α-51D gene has been determined, as well as the upstream and downstream noncoding regions. Its deduced amino acid sequence shows the same characteristic cysteine periodicity displayed by all other immobilization antigen (i-ag) genes from Paramecium. However, in contrast to most other such genes, tandem repeats are missing from the 7599-bp long coding region of the α-51D gene. When the sequences of the type 51D genes are compared to each other, the similarity is very high and extends to coding as well as to noncoding regions. Similarity within noncoding regions is usually only observed for allelic i-ag genes. We conclude that the type D genes constitute a family of isogenes that are nonallelic. They contain slightly different consensus sequences with possible functions as regulatory regions.
Keywords:Cysteine periodicity  immobilization antigen  isogenes
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号