TY - JOUR
T1 - Schistosoma japonicum
T2 - Analysis of eggshell protein genes, their expression, and comparison with similar genes from other schistosomes
AU - Bobek, Libuse A.
AU - Rekosh, David M.
AU - Lo Verde, Philip T.
N1 - Funding Information:
We thank Dr. George Watt, NAMRU 2, for supplying field-collected0 . hupensis quadrasi, Hong Shi for technicala ssistance,a nd Theresa Wnuk for outstanding secretarials ervice. Some of the S. japonicum materials used in this study were provided by an NIAID supply contract (AI 052590)T. his research was supported in part by grants from NIAID (AI 18867,A I 127219a) nd the Edna McConnell Clark Foundation. D.M.R. is the recipient of a Research Career Development Award CA-000905 fromt he NIH. This work was conducteda s part of the Center for Applied Molecular Biology and Immunologyo f the State University of New York at Buffalo.
PY - 1991/5
Y1 - 1991/5
N2 - As the egg of Schistosoma japonicum plays a central role in transmission and in pathogenesis, we sought to understand the molecular biology of egg formation. In this study we characterized an eggshell protein gene of S. japonicum and compared it with similar genes from S. mansoni and S. haematobium. To initiate studies on the eggshell protein genes of S. japonicum, a cloned genomic fragment containing an entire copy of a S. haematobium eggshell protein gene was used to identify three EcoRI hybridizing fragments of 2.6, 2.0, and 1.3 kbp in S. japonicum genomic DNA and to isolate three independent genomic clones from a S. japonicum genomic library. Two genomic clones, SJ 4-1 and SJ 3-1, contain at least two copies of the gene. The DNA sequence of a 2.0-kbp EcoRI fragment of clone SJ 3-1 showed two open reading frames (ORF), one of which showed a strong homology to the chorion proteins of insects. This ORF had 207 amino acids with a calculated molecular size of 18.5 kDa. The predicted peptide was glycine (50%) and tyrosine (10%) rich like other described schistosome eggshell proteins. Primer extension and the dideoxynucleotide sequence of the mRNA defined the cap site of the RNA and positioned the putative TATA and CAAAT elements and other cis-acting elements. Northern analysis demonstrated that eggshell protein mRNA was only detected in mature female parasites. The appearance of the female-specific mRNA was dependent on pairing with the male parasite and increased with egg production (as determined by hybridization intensity). A comparison of the DNA and deduced protein sequences of eggshell protein genes from S. japonicum with those of similar genes from S. mansoni and S. haematobium indicated that the genes are highly conserved, with S. mansoni and S. haematobium genes being more similar to each other than either is to S. japonicum.
AB - As the egg of Schistosoma japonicum plays a central role in transmission and in pathogenesis, we sought to understand the molecular biology of egg formation. In this study we characterized an eggshell protein gene of S. japonicum and compared it with similar genes from S. mansoni and S. haematobium. To initiate studies on the eggshell protein genes of S. japonicum, a cloned genomic fragment containing an entire copy of a S. haematobium eggshell protein gene was used to identify three EcoRI hybridizing fragments of 2.6, 2.0, and 1.3 kbp in S. japonicum genomic DNA and to isolate three independent genomic clones from a S. japonicum genomic library. Two genomic clones, SJ 4-1 and SJ 3-1, contain at least two copies of the gene. The DNA sequence of a 2.0-kbp EcoRI fragment of clone SJ 3-1 showed two open reading frames (ORF), one of which showed a strong homology to the chorion proteins of insects. This ORF had 207 amino acids with a calculated molecular size of 18.5 kDa. The predicted peptide was glycine (50%) and tyrosine (10%) rich like other described schistosome eggshell proteins. Primer extension and the dideoxynucleotide sequence of the mRNA defined the cap site of the RNA and positioned the putative TATA and CAAAT elements and other cis-acting elements. Northern analysis demonstrated that eggshell protein mRNA was only detected in mature female parasites. The appearance of the female-specific mRNA was dependent on pairing with the male parasite and increased with egg production (as determined by hybridization intensity). A comparison of the DNA and deduced protein sequences of eggshell protein genes from S. japonicum with those of similar genes from S. mansoni and S. haematobium indicated that the genes are highly conserved, with S. mansoni and S. haematobium genes being more similar to each other than either is to S. japonicum.
KW - Chorion genes
KW - DNA and protein sequence comparisons
KW - Developmentally regulated expression
KW - Eggshell protein genes
KW - Schistosoma haematobium
KW - Schistosoma japonicum
KW - Schistosoma mansoni
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U2 - 10.1016/0014-4894(91)90084-A
DO - 10.1016/0014-4894(91)90084-A
M3 - Article
C2 - 1709112
AN - SCOPUS:0026166448
SN - 0014-4894
VL - 72
SP - 381
EP - 390
JO - Experimental Parasitology
JF - Experimental Parasitology
IS - 4
ER -