The recombination and thus have a larger number of clones represented in the T-cell repertoire. Further, the consistency observed in the frequency of specific TRB V and J segment usage across several unrelated donors and patients reconstituting T cells following SCT provides greater confidence in the reproducibility of this observation.4. DiscussionThe germ-line genomic TCR (and immunoglobulin) loci have the unique characteristic in that these can undergo DNA double strand break and recombination resulting in VDJ rearrangement which results in the generation of numerous unique T-cell (and B-cell) clones with the ability to identify a wide array of antigens. In this analytical manuscript, characteristics of the organization of TCR gene segments are explored, and spatial symmetry identified across regions of these loci. Further, the possible relationships between the periodic occurrence of the TCR gene segments and its potential influence on T-cell clonal frequency are also investigated. It is found that the TCR loci are organized with mathematical precision, which suggests that T-cell repertoire formation may be a deterministic process.TCR rearrangement is an ordered process, with the sequence of recombinatorial events Y-27632 biological activity governed by DNA sequence motifs occurring at regular frequency in the TCR loci. The so-called `12/23 rule’ is an example of this, where the TRB V, D and J segments are flanked by conserved sequences called recombination signal sequences (RSS), comprised a heptameric and a nonameric sequence, which are interposed by either a 12 (RSS-12) or a 23 (RSS-23) base pair sequence. VDJ rearrangement is Y-27632 cost brought about by recombinase-activating gene-1 (RAG-1) and RAG-2 protein complexes, which always bring together segments with a Miransertib site RSS-12 with a segment flanked by a RSS-23, not otherwise. Considering the TRB, Db segments are flanked by the RSS sequences on both sides (50 , RSS-12 and 30 , RSS-23), Jb segments on the 50 end (RSS-12) and Vb segments on the 30 end (RSS-23) [25]. In the series of events set off during T-cell development, initially a Db segment rearranges with one of the Jb segments, then the combined DJb joins with a specific Vb segment to LM22A-4 site result in VDJb rearrangement, yielding a unique T-cell clone. Similar considerations hold for TCRa, where Ja recombines with Va, with the additional possibility of locus editing such that alternative 50 Va may be rearranged to an alternative 30 Ja segment at a later time [26]. As elegant as this system is, it does not completely explain either how the order of recombination is determined or what determines the variability in the use of various TCR gene segments encountered in the T-cell repertoire; for instance, why does theDb RSS-23 preferentially rearrange with Jb RSS-12, and not the Db RSS-12 with the Vb RSS-23, and, why are clones with TRB V5-1 encountered much more frequently than TRB V5-4 in the normal T-cell repertoire? Further, under normal circumstances, in the rearrangement of the TRD (TCR-d) locus, some V segments in this and the TRA locus recombine only with TRD-D, while others recombine both with TRD-D and TRA-J segments [27], despite the TRD locus being nested within the TRA locus. Further, when a TRA-Ja segment is ectopically introduced in the TRD locus at the TRD-Dd segment position, rearrangement of this ectopic TRA-J with TRD-V segments occurs, demonstrating that locus position, rather than the actual sequence may have a deterministic role in the order of recombination [.The recombination and thus have a larger number of clones represented in the T-cell repertoire. Further, the consistency observed in the frequency of specific TRB V and J segment usage across several unrelated donors and patients reconstituting T cells following SCT provides greater confidence in the reproducibility of this observation.4. DiscussionThe germ-line genomic TCR (and immunoglobulin) loci have the unique characteristic in that these can undergo DNA double strand break and recombination resulting in VDJ rearrangement which results in the generation of numerous unique T-cell (and B-cell) clones with the ability to identify a wide array of antigens. In this analytical manuscript, characteristics of the organization of TCR gene segments are explored, and spatial symmetry identified across regions of these loci. Further, the possible relationships between the periodic occurrence of the TCR gene segments and its potential influence on T-cell clonal frequency are also investigated. It is found that the TCR loci are organized with mathematical precision, which suggests that T-cell repertoire formation may be a deterministic process.TCR rearrangement is an ordered process, with the sequence of recombinatorial events governed by DNA sequence motifs occurring at regular frequency in the TCR loci. The so-called `12/23 rule’ is an example of this, where the TRB V, D and J segments are flanked by conserved sequences called recombination signal sequences (RSS), comprised a heptameric and a nonameric sequence, which are interposed by either a 12 (RSS-12) or a 23 (RSS-23) base pair sequence. VDJ rearrangement is brought about by recombinase-activating gene-1 (RAG-1) and RAG-2 protein complexes, which always bring together segments with a RSS-12 with a segment flanked by a RSS-23, not otherwise. Considering the TRB, Db segments are flanked by the RSS sequences on both sides (50 , RSS-12 and 30 , RSS-23), Jb segments on the 50 end (RSS-12) and Vb segments on the 30 end (RSS-23) [25]. In the series of events set off during T-cell development, initially a Db segment rearranges with one of the Jb segments, then the combined DJb joins with a specific Vb segment to result in VDJb rearrangement, yielding a unique T-cell clone. Similar considerations hold for TCRa, where Ja recombines with Va, with the additional possibility of locus editing such that alternative 50 Va may be rearranged to an alternative 30 Ja segment at a later time [26]. As elegant as this system is, it does not completely explain either how the order of recombination is determined or what determines the variability in the use of various TCR gene segments encountered in the T-cell repertoire; for instance, why does theDb RSS-23 preferentially rearrange with Jb RSS-12, and not the Db RSS-12 with the Vb RSS-23, and, why are clones with TRB V5-1 encountered much more frequently than TRB V5-4 in the normal T-cell repertoire? Further, under normal circumstances, in the rearrangement of the TRD (TCR-d) locus, some V segments in this and the TRA locus recombine only with TRD-D, while others recombine both with TRD-D and TRA-J segments [27], despite the TRD locus being nested within the TRA locus. Further, when a TRA-Ja segment is ectopically introduced in the TRD locus at the TRD-Dd segment position, rearrangement of this ectopic TRA-J with TRD-V segments occurs, demonstrating that locus position, rather than the actual sequence may have a deterministic role in the order of recombination [.The recombination and thus have a larger number of clones represented in the T-cell repertoire. Further, the consistency observed in the frequency of specific TRB V and J segment usage across several unrelated donors and patients reconstituting T cells following SCT provides greater confidence in the reproducibility of this observation.4. DiscussionThe germ-line genomic TCR (and immunoglobulin) loci have the unique characteristic in that these can undergo DNA double strand break and recombination resulting in VDJ rearrangement which results in the generation of numerous unique T-cell (and B-cell) clones with the ability to identify a wide array of antigens. In this analytical manuscript, characteristics of the organization of TCR gene segments are explored, and spatial symmetry identified across regions of these loci. Further, the possible relationships between the periodic occurrence of the TCR gene segments and its potential influence on T-cell clonal frequency are also investigated. It is found that the TCR loci are organized with mathematical precision, which suggests that T-cell repertoire formation may be a deterministic process.TCR rearrangement is an ordered process, with the sequence of recombinatorial events governed by DNA sequence motifs occurring at regular frequency in the TCR loci. The so-called `12/23 rule’ is an example of this, where the TRB V, D and J segments are flanked by conserved sequences called recombination signal sequences (RSS), comprised a heptameric and a nonameric sequence, which are interposed by either a 12 (RSS-12) or a 23 (RSS-23) base pair sequence. VDJ rearrangement is brought about by recombinase-activating gene-1 (RAG-1) and RAG-2 protein complexes, which always bring together segments with a RSS-12 with a segment flanked by a RSS-23, not otherwise. Considering the TRB, Db segments are flanked by the RSS sequences on both sides (50 , RSS-12 and 30 , RSS-23), Jb segments on the 50 end (RSS-12) and Vb segments on the 30 end (RSS-23) [25]. In the series of events set off during T-cell development, initially a Db segment rearranges with one of the Jb segments, then the combined DJb joins with a specific Vb segment to result in VDJb rearrangement, yielding a unique T-cell clone. Similar considerations hold for TCRa, where Ja recombines with Va, with the additional possibility of locus editing such that alternative 50 Va may be rearranged to an alternative 30 Ja segment at a later time [26]. As elegant as this system is, it does not completely explain either how the order of recombination is determined or what determines the variability in the use of various TCR gene segments encountered in the T-cell repertoire; for instance, why does theDb RSS-23 preferentially rearrange with Jb RSS-12, and not the Db RSS-12 with the Vb RSS-23, and, why are clones with TRB V5-1 encountered much more frequently than TRB V5-4 in the normal T-cell repertoire? Further, under normal circumstances, in the rearrangement of the TRD (TCR-d) locus, some V segments in this and the TRA locus recombine only with TRD-D, while others recombine both with TRD-D and TRA-J segments [27], despite the TRD locus being nested within the TRA locus. Further, when a TRA-Ja segment is ectopically introduced in the TRD locus at the TRD-Dd segment position, rearrangement of this ectopic TRA-J with TRD-V segments occurs, demonstrating that locus position, rather than the actual sequence may have a deterministic role in the order of recombination [.The recombination and thus have a larger number of clones represented in the T-cell repertoire. Further, the consistency observed in the frequency of specific TRB V and J segment usage across several unrelated donors and patients reconstituting T cells following SCT provides greater confidence in the reproducibility of this observation.4. DiscussionThe germ-line genomic TCR (and immunoglobulin) loci have the unique characteristic in that these can undergo DNA double strand break and recombination resulting in VDJ rearrangement which results in the generation of numerous unique T-cell (and B-cell) clones with the ability to identify a wide array of antigens. In this analytical manuscript, characteristics of the organization of TCR gene segments are explored, and spatial symmetry identified across regions of these loci. Further, the possible relationships between the periodic occurrence of the TCR gene segments and its potential influence on T-cell clonal frequency are also investigated. It is found that the TCR loci are organized with mathematical precision, which suggests that T-cell repertoire formation may be a deterministic process.TCR rearrangement is an ordered process, with the sequence of recombinatorial events governed by DNA sequence motifs occurring at regular frequency in the TCR loci. The so-called `12/23 rule’ is an example of this, where the TRB V, D and J segments are flanked by conserved sequences called recombination signal sequences (RSS), comprised a heptameric and a nonameric sequence, which are interposed by either a 12 (RSS-12) or a 23 (RSS-23) base pair sequence. VDJ rearrangement is brought about by recombinase-activating gene-1 (RAG-1) and RAG-2 protein complexes, which always bring together segments with a RSS-12 with a segment flanked by a RSS-23, not otherwise. Considering the TRB, Db segments are flanked by the RSS sequences on both sides (50 , RSS-12 and 30 , RSS-23), Jb segments on the 50 end (RSS-12) and Vb segments on the 30 end (RSS-23) [25]. In the series of events set off during T-cell development, initially a Db segment rearranges with one of the Jb segments, then the combined DJb joins with a specific Vb segment to result in VDJb rearrangement, yielding a unique T-cell clone. Similar considerations hold for TCRa, where Ja recombines with Va, with the additional possibility of locus editing such that alternative 50 Va may be rearranged to an alternative 30 Ja segment at a later time [26]. As elegant as this system is, it does not completely explain either how the order of recombination is determined or what determines the variability in the use of various TCR gene segments encountered in the T-cell repertoire; for instance, why does theDb RSS-23 preferentially rearrange with Jb RSS-12, and not the Db RSS-12 with the Vb RSS-23, and, why are clones with TRB V5-1 encountered much more frequently than TRB V5-4 in the normal T-cell repertoire? Further, under normal circumstances, in the rearrangement of the TRD (TCR-d) locus, some V segments in this and the TRA locus recombine only with TRD-D, while others recombine both with TRD-D and TRA-J segments [27], despite the TRD locus being nested within the TRA locus. Further, when a TRA-Ja segment is ectopically introduced in the TRD locus at the TRD-Dd segment position, rearrangement of this ectopic TRA-J with TRD-V segments occurs, demonstrating that locus position, rather than the actual sequence may have a deterministic role in the order of recombination [.
