The immune system produces a huge variety – hundreds of billions – of high-affinity antibodies. Immunologists have been asking how B cells accomplish this for decades, and in the past five years, the answers have come, all in a rush. A single enzyme, it appears, mutates DNA to control two very different diversifying phenomena: hypermutation of the variable region and class switch recombination.
"It's beautiful because there's this really old problem and it's finally solved," says Michel Nussenzweig, a molecular immunologist at Rockefeller University in New York City. "And it's solved in such a minimal way," he adds, with one enzyme and three reactions.
The enzyme, activation induced deaminase (AID), was described in 2000.1 Early evidence that DNA, rather than RNA, was the substrate appeared in 2002.2 The next logical step was to make the enzyme work in a biochemical assay. Three of this issue's four Hot Papers...
BIOCHEMISTRY OF AID
Data derived from the Science Watch / Hot Papers database and the Web of Science (Thomson Scientific, Philadelphia) show that Hot Papers are cited 50 to 100 times more often than the average paper of the same type and age.
"These are enzymes that are not easy to work with," says Michael Neuberger of the Laboratory of Molecular Biology, Cambridge, UK. Only present in relatively small amounts in B cells, AID is both inactive and insoluble when made in a test tube, he adds. "There's a lot going on that keeps its activity in check," which makes sense for a protein that causes gene mutation. "And so the business of showing catalytic activity on DNA was nontrivial," says Neuberger.
Because early reports had failed to show activity for the enzyme on RNA, singled-stranded (ss) DNA, or double-stranded (ds) DNA, University of Southern California biologist Myron Goodman thought he'd try something different: a RNA-DNA hybrid. His group's Hot Paper reports activity only when the RNA strand was digested with an RNAse.3 So AID was not working on the hybrid directly, but rather while another enzyme destroyed the RNA strand, the RNAse was "allowing AID to do what it does," says Goodman.
The study also confirmed earlier predictions that AID changes cytosine to uracil, says Patricia Gearhart, an immunologist at the National Institute on Aging in Bethesda, Md. But Goodman's demonstration was not definitive; AID purifications were incomplete, leaving the possibility that other factors were responsible for the observed activity. Also, it was expressed as a glutathione-S-transferase fusion protein in insect cells. "People were saying it could still be RNA editing if you had the real AID protein, instead of this artificial thing," says Gearhart.
Two weeks later, Fred Alt's paper appeared using the real thing: AID highly purified from mammalian B cells. He also reported activity on ssDNA, not dsDNA or RNA, generating uracil.4 Alt, a molecular immunologist at Harvard's Children's Hospital, credits his coauthor, Jayanta Chaudhuri, now at Memorial Sloan Kettering Cancer Center in New York City, with the "intuition and insight" that AID might require modification to be active. "So the idea was to get AID from a source where we knew it should be fully active in the processes for which it was supposed to work," says Alt. Alt's experiments also induced transcription to see AID activity. "That got everyone tuned into transcription," says Gearhart.
A third biochemical study, by Nina Papavasiliou at Rockefeller University, used AID purified from
GENETICS OF AID
Neuberger's work in 2002 first turned everybody's attention to DNA.6 "What Michael did was to express AID in
In this issue's fourth Hot Paper, Nussenzweig showed that DNA actually was the substrate for the enzyme in this system. He used an inducible promotor on a gene, and "when we induced the gene, we got more mutation," he says.7 Thus, ssDNA created during transcription was the substrate for AID. "Transcription is important because it liberates the substrate."
© 2004 Nature Publishing Group
Activation-induced cytidine deaminase (AID) deaminates cytidine residues in DNA, converting them into uridine. The U-G mismatch can then be processed either by base excision repair (BER) or mismatch repair (MMR). In somatic hypermutation, the mismatch can be replicated to produce a C-to-T mutation, nick processing by UNG can produce an abasic site, or a gap can be filled in by error prone polymerases. During ' class-switch recombination, stag' gered nicks are thought to be processed by unknown exonucleases or error-prone end-filling leading to blunt double-strand breaks that can be ligated to similarly created breaks on the downstream. (Adapted from M. Nussenzweig, F.W. Alt,
Both Neuberger and Nussenzweig exploited a key feature of the
Researchers allow that not all doubt has been put to rest. Tasuku Honjo, whose group at Kyoto University originally described AID, still uses an RNA-editing mechanism to explain AID action. Enzymes related to AID (known as APOBEC family proteins) use this mechanism, and when put into
AID IN TARGETING
Meanwhile, researchers are building the DNA case. The fact that enzyme activity was related to transcription "suggests that the targeting to immunoglobulin genes may be related to the higher amounts of transcription," says Gearhart. "So now all of a sudden everyone's thinking targeting."
Regulation of a process as potentially damaging as DNA hypermutation is obviously an important issue. Alt has identified one potential regulatory factor, replication protein A, a ssDNA binding protein.8
AID can clearly work on both strands of DNA, despite early evidence that the enzyme targets only the nontemplate strand. Biochemically, AID has specificity for certain DNA base sequences in immunoglobulin genes known to be mutational hot spots. Whether AID induces point mutation or double-strand breaks may depend on the frequency of a three-base sequence known as WRC. In the variable region of the gene, processing of an abasic site (after the U is excised) by mistmatch repair or error-prone polymerase results in mutation. A higher frequency of WRC motifs in the switch region increase the likelihood that abasic sites result in stagger breaks and the recombination that underlies class switch.
"What's really nice about all this work is that it ties together in vivo phenotypic observations of hypermutation, which we've known for about 20 years now, [with] these beautiful genetics experiments and biochemistry," says Gearhart. Perhaps it is a case where a field has been looking for answers for so long, that once there was a useful clue, everything seemed to fall into place.