LIGHT CHAIN

1. C n t n Ig Polypeptides Are Encoded by Multiple Gene Segments LIGHT CHAIN Polypeptide Light Chain POLYPEPTIDE Gene Segments Light Chain GENE SEGMENTS HEAVY CHAIN o s a t Polypeptide V a r i a b l e H.C.POLYPEPTIDE C C C V Gene Segments D J H 1 H 3 H 2 H.C. GENE SEGMENTS

2. A Prototype Ig Gene: Murine Kappa 4 J Gene About 10 0 1 C Gene k Segment s V gene segments Segmen t k Multiple V gene segments, distant from J and C A few J gene segments One C gene segment

3. Heavy Chain Gene Organization Murine Ig ~ 120 V 8 Constant Gene Segments 4 Js ~20 Ds Gene Segments C C 2b C C 3 C 1 C C 2a C m g d g g e g a V L H C 1 C 2 C 3 C 4/S C M m m m m m

4. Figure 4-4 Human Ig Loci

5. TCR Alpha and Beta Loci

6. TCR Delta and Gamma Loci

7. IMMUNOGLOBULIN GENES UNDERGO TWODNA REARRANGEMENTS V(D)J Recombination: both light and heavy chains Class switch recombination: heavy chains only

8. Figure 4-2 DNA Rearrangement RemovesSequences Between V, D and J Segments RNA Splicing Removes Sequences Between J and C Segments DNA RNA

9. Figure 4-6 V(D)J recombination involves DELETION of DNA between V, D and J coding segments. The deleted DNA is LOST from the cell because it is not replicated.

10. Figure 4-5 Recombination Signal Sequences (RSSs) Flank Rearranging Gene Segments RSS=heptamer, spacer and nonamer 7bp 9bp 12/23 bp

11. Figure 4-7 #1: Lymphocyte- Specific #2: Constitutive Initiation of V(D)J rearrangement :RAG- dependent cleavage Resolution of cleavage products: DNA non- homologous end-joining machinery

12. Addition of Bases at V-D-J Junctions: An Important Source of Diversity Figure 4-8

13. Figure 7-18

14. CONSEQUENCES OF V(D)J RECOMBINATION Combinatorial diversity: # of possible combinations is the product of the # of recombining segments i.e. for mouse h.c.: 120x20x4=104 2. Junctional diversity at CDR3 Deletion of bases at junctions N region additions at junctions P region additions at junctions 3. Activates transcription of the rearranged gene Juxtaposition of intronic enhancers with V region promoters. 4. Allows receptor editing to alter potentially self-reactive antibodies

15. C n t n Ig Polypeptides Are Encoded by Multiple Gene Segments LIGHT CHAIN Polypeptide Light Chain POLYPEPTIDE Gene Segments Light Chain GENE SEGMENTS HEAVY CHAIN o s a t Polypeptide V a r i a b l e H.C.POLYPEPTIDE C C C V Gene Segments D J H 1 H 3 H 2 H.C. GENE SEGMENTS

16. Heavy chain isotypes are generated by a second DNA rearrangement: CLASS SWITCH RECOMBINATION (CSR)

17. Figure 4-18

18. Figure 4-17

19. Figure 4-19 mRNA Splicing DNA rearrangement: CSR

20. Figure 4-20 IgM and IgD Are Generated from a Single Primary Transcript by DIFFERENTIAL mRNA POLY A/SPLICING

21. Membrane vs. Secreted Mu mRNAs encoding both membrane and secreted forms of mu heavy chain are gen- erated from a single primary transcript by differential splicing and polyadenylation

22. Figure 4-21 CSR Involves DNA Deletion and Loss

23. “Germline” (I region) Transcripts Are Necessary For Isotype Switch Recombination

24. Figure 9-7

25. T cell secretes cytokines TGF Specific I region transcription IaSaCaRNA Isotype switch recombination to specific CH gene segment Cut and join Sm and SaDNA VDJCa mRNA IgA

26. V(D)J Recombination CSR Join in exon Join in intron RAGs required RAGs Not required AID is required Repair enzymes Repair enzymes Generates diversity Changes isotype Ag specificity Ag elimination Regulated by T cell signals Random

27. 1. Humans with mutations in gene products required for V(D)J recombination are immunodeficient: RAG Various SCIDs, including Omenn’s syndrome Artemis Radio-sensitive SCID Ligase IV SCID with developmental deficiency 2. Humans with mutations affecting CSR have hyper IgM AID mutations and other mutations