Genomic organization and chromosomal localization of the human CD27 gene.

CD27 is a lymphocyte-specific member of a recently identified receptor family with at least 10 members that includes the receptors for nerve growth factor and TNF, CD40, and Fas. Several members of this family play a role in cell differentiation, proliferation, and survival. Within the amino terminal ligand binding domain of these receptors, repeat motifs have been identified. These repeats contain many cysteine residues in a conserved pattern, characteristic of this family. We have isolated and characterized the human CD27 gene to gain insight into the evolution of this type of receptor domain. The gene was localized on chromosome 12, band 12p13. Sequence analysis showed no correlation between the intron/exon organization and the subdivision of the protein into distinct domains. Structural information for the cysteine-rich domain is contained within three exons. In addition, the splice sites in the CD27 gene are located in a different position from those in the related nerve growth factor receptor gene. However, a comparison of the splice sites within the regions encoding the respective ligand-binding domains of the CD27 and nerve growth factor receptor genes identifies the archetypal cysteine-rich building blocks, from which the members of this family may have arisen during the course of evolution. From this observation, we propose a new organization of the repeat motifs.

[1]  H. Stein,et al.  Molecular cloning and expression of a new member of the nerve growth factor receptor family that is characteristic for Hodgkin's disease , 1992, Cell.

[2]  G. Wong,et al.  Molecular cloning and expression of a receptor for human tumor necrosis factor , 1990, Cell.

[3]  H. Tabuchi,et al.  Molecular cloning and expression of the human 55 kd tumor necrosis factor receptor , 1990, Cell.

[4]  R. V. van Lier,et al.  Alternative molecular form of human T cell‐specific antigen CD27 expressed upon T cell activation , 1989, European journal of immunology.

[5]  G. Crabtree Contingent genetic regulatory events in T lymphocyte activation. , 1989, Science.

[6]  A. E. Sippel,et al.  Viral myb oncogene encodes a sequence-specific DNA-binding activity , 1988, Nature.

[7]  M. Chao,et al.  A constitutive promoter directs expression of the nerve growth factor receptor gene. , 1988, Molecular and cellular biology.

[8]  P. Sharp,et al.  Human CCAAT-binding proteins have heterologous subunits , 1988, Cell.

[9]  D. Lipman,et al.  Improved tools for biological sequence comparison. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[10]  R. Levi‐montalcini,et al.  The nerve growth factor 35 years later. , 1987, Science.

[11]  C. Richardson,et al.  DNA sequence analysis with a modified bacteriophage T7 DNA polymerase. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[12]  P. Nowell,et al.  Sequential expression of protooncogenes during lectin-stimulated mitogenesis of normal human lymphocytes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[13]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[14]  A. F. Williams,et al.  The immunoglobulin superfamily--domains for cell surface recognition. , 1988, Annual review of immunology.

[15]  N. Murray Phage Lambda and Molecular Cloning , 1983 .