TY - JOUR
T1 - Porcine Fas-ligand gene
T2 - Genomic sequence analysis and comparison with human gene
AU - Motegi-Ishiyama, Yukari
AU - Nakajima, Yoichi
AU - Hoka, Sumio
AU - Takagaki, Yohtaroh
N1 - Funding Information:
The authors would like to thank Hiromi Hatsuse for administrative and technical assistance, and K. Takagaki for critical reading of the manuscript. This research was supported in part by the Academic Frontier Project of the Ministry of Education, Science, Sports and Culture of Japan.
PY - 2002
Y1 - 2002
N2 - Thymic Fas-ligand (FasL) cDNA and hepatic FasL genomic sequences were obtained from a 2-month-old LW pig. From these nucleotide sequences, amino acid sequence was deduced and compared with FasL sequences obtained from various animals. This comparison reveals that porcine FasL is closer to that of human, macaca and cat, and differs more from mouse and rat. The extracelluar domains of porcine and human FasL proteins appear to be functionally compatible. The complete genomic DNA sequence of porcine FasL was also compared with its human counterpart. Exons showed 80-89% nucleotide homology between pig and human, while introns showed 64-69% nucleotide homology. Sequence comparison by Harr plot analysis revealed many stretches within introns having identical sequences, suggesting that the sites may have unidentified common functions. One potential extra exon between exons 2 and 3 was located within porcine intron 2. This potential exon has no counterpart in human FasL intron 2. Whether or not this extra exon can be expressed and could cause additional immunological responses remains to be investigated. For future xenotransplantation, it is important to compare porcine and human genomic sequences, and to investigate their system compatibilities.
AB - Thymic Fas-ligand (FasL) cDNA and hepatic FasL genomic sequences were obtained from a 2-month-old LW pig. From these nucleotide sequences, amino acid sequence was deduced and compared with FasL sequences obtained from various animals. This comparison reveals that porcine FasL is closer to that of human, macaca and cat, and differs more from mouse and rat. The extracelluar domains of porcine and human FasL proteins appear to be functionally compatible. The complete genomic DNA sequence of porcine FasL was also compared with its human counterpart. Exons showed 80-89% nucleotide homology between pig and human, while introns showed 64-69% nucleotide homology. Sequence comparison by Harr plot analysis revealed many stretches within introns having identical sequences, suggesting that the sites may have unidentified common functions. One potential extra exon between exons 2 and 3 was located within porcine intron 2. This potential exon has no counterpart in human FasL intron 2. Whether or not this extra exon can be expressed and could cause additional immunological responses remains to be investigated. For future xenotransplantation, it is important to compare porcine and human genomic sequences, and to investigate their system compatibilities.
UR - https://www.scopus.com/pages/publications/0036162748
UR - https://www.scopus.com/pages/publications/0036162748#tab=citedBy
U2 - 10.1016/S0161-5890(01)00098-0
DO - 10.1016/S0161-5890(01)00098-0
M3 - Article
C2 - 11792426
AN - SCOPUS:0036162748
SN - 0161-5890
VL - 38
SP - 581
EP - 586
JO - Molecular Immunology
JF - Molecular Immunology
IS - 8
ER -