RAPID CLONING OF ANY REARRANGED MOUSE IMMUNOGLOBULIN VARIABLE GENES

Immunoglobulins (Ig) have been the focus of extensive study for severa l decades and have become an important research area for immunologists and molecular biologists. The use of polymerase chain reaction (PCR) technology has accelerated the cloning, sequencing, and characterizati on of genes of the immune system. However, cloning and sequencing the Ig variable (V) genes using the PCR technology has been a challenging task, primarily due to the very diverse nature of Ig V region genes. W e have developed a simple, rapid, and reproducible PCR-based technique to clone any rearranged mouse Ig heavy or light chain genes. A close examination of all Ig heavy and light chain V gene families has result ed in the design of 5' and 3' universal primers from regions that are highly conserved across all heavy or light chain V gene families, and the joining or constant regions, respectively. We present our strategy for designing universal primers for Ig V gene families. These primers were able to rapidly amplify the rearranged Ig V genes, belonging to diverse Ig V gene families from very different cell lines, i. e., J558 , MOPC-21, 36-60, and a chicken ovalbumin specific B-cell hybridoma. I n addition, the present study provides the complete alignment of nucle otide sequences of all heavy and light chain variable gene families. T his powerful method of cloning Ig V genes, therefore, allows rapid and precise analysis of B-cell hybridomas, B-cell repertoire, and B-cell ontogeny.