TY - JOUR
T1 - MU switch region deletion is associated with both T cell independent and T cell dependent responses
AU - Mukherjee, Jean
AU - Casadevall, Arturo
AU - Scharff, Matthew D.
N1 - Funding Information:
M. D. S. is supported in part by the Harry Eagle Chair provided by the Women’s Division of Albert Einstein College of Medicine. A. C. was supported by a Pfizer Postdoctoral Fellowship. The data in this paper are from a thesis submitted by J. M. in partial fulfillment of the requirements of the Degree of Doctor of Philosophy in the Sue Golding Graduate Division of Medical Science, Albert Einstein College of Medicine, Yeshiva University. $Author to whom correspondence should be addressed.
PY - 1993/8
Y1 - 1993/8
N2 - Isotype switching is a process by which immunoglobulin variable gene regions initially proximal to and expressed with the mu constant region gene (Cμ) can rearrange downstream to other constant region genes. Thus the same antigen binding site can be expressed with each of the other constant region isotypes and perform the full panoply of effector functions. Although isotype switching is thought to involve highly reiterated 'switch site' sequences located 5' to constant region genes, the exact role of these switch sites is unknown. It has been reported that prior to switching, the 'donor' switch site 5' of Cμ occasionally undergoes deletions, but it is not known whether this is an adventitious event or one which predisposes to or prevents isotype switching. Since T cell independent (TI) immune responses are dominated by IgM while T cell dependent (TD) responses are associated with switching to IgG, we have examined the state of the mu switch site in 51 IgM-producing hybridomas isolated from a variety of TI and TD responses. Although more hybridomas from the TI responses studied exhibited Sμ deletions, deletion of Sμ also occurred in hybridomas isolated from TD responses. Analysis of a well-characterized clonally related subset of IgM hybridomas also revealed that mu switch region deletion can be associated with the productive allele.
AB - Isotype switching is a process by which immunoglobulin variable gene regions initially proximal to and expressed with the mu constant region gene (Cμ) can rearrange downstream to other constant region genes. Thus the same antigen binding site can be expressed with each of the other constant region isotypes and perform the full panoply of effector functions. Although isotype switching is thought to involve highly reiterated 'switch site' sequences located 5' to constant region genes, the exact role of these switch sites is unknown. It has been reported that prior to switching, the 'donor' switch site 5' of Cμ occasionally undergoes deletions, but it is not known whether this is an adventitious event or one which predisposes to or prevents isotype switching. Since T cell independent (TI) immune responses are dominated by IgM while T cell dependent (TD) responses are associated with switching to IgG, we have examined the state of the mu switch site in 51 IgM-producing hybridomas isolated from a variety of TI and TD responses. Although more hybridomas from the TI responses studied exhibited Sμ deletions, deletion of Sμ also occurred in hybridomas isolated from TD responses. Analysis of a well-characterized clonally related subset of IgM hybridomas also revealed that mu switch region deletion can be associated with the productive allele.
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U2 - 10.1016/0161-5890(93)90130-4
DO - 10.1016/0161-5890(93)90130-4
M3 - Article
C2 - 8350875
AN - SCOPUS:0027527410
SN - 0161-5890
VL - 30
SP - 1049
EP - 1055
JO - Molecular Immunology
JF - Molecular Immunology
IS - 11
ER -