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The Role of the RAG1 Non-Core Domain...
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Beilinson, Helen Alexander.
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The Role of the RAG1 Non-Core Domain in V(D)J Recombination and Lymphocyte Development.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
The Role of the RAG1 Non-Core Domain in V(D)J Recombination and Lymphocyte Development./
作者:
Beilinson, Helen Alexander.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2021,
面頁冊數:
294 p.
附註:
Source: Dissertations Abstracts International, Volume: 83-02, Section: B.
Contained By:
Dissertations Abstracts International83-02B.
標題:
Immunology. -
電子資源:
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28315434
ISBN:
9798522948207
The Role of the RAG1 Non-Core Domain in V(D)J Recombination and Lymphocyte Development.
Beilinson, Helen Alexander.
The Role of the RAG1 Non-Core Domain in V(D)J Recombination and Lymphocyte Development.
- Ann Arbor : ProQuest Dissertations & Theses, 2021 - 294 p.
Source: Dissertations Abstracts International, Volume: 83-02, Section: B.
Thesis (Ph.D.)--Yale University, 2021.
This item must not be sold to any third party vendors.
Immunoglobulin and T cell receptor gene assembly depend on V(D)J recombination initiated by the RAG1-RAG2 recombinase. The RAG1 N-terminal region (NTR; aa 1-383) has been implicated in regulatory functions whose influence on V(D)J recombination and lymphocyte development in vivo are poorly understood. We generated mouse strains in which RAG1 lacks its first 215 residues (Δ215), E3 ubiquitin ligase activity (P326G), or the major site of autoubiquitination (K233R). RAG1 protein levels are increased in all three mutants and RAG1-P326G B cells exhibit increased cell death during development and an increased lgK:lgλ ratio. Previous studies have demonstrated that recombination of the immunoglobulin heavy chain gene (Igh) occurs by two distinct reaction modes: long-range, cohesin-dependent scanning and short-range collision. We find that RAG1Δ215 mice exhibit reduced short-range Igh D-to-J recombination. In addition, we find the V gene segment repertoire is altered in RAG1Δ215 mice at the Igh and IgK loci, while loss of integrity of the E3 ubiquitin ligase domain leads to a decrease in out-of-frame recombination events at the Igh locus.We also demonstrate preliminary findings indicating that off-target recombination events may also be dictated by the same mechanisms of short- and long-range recombination. Our findings indicate that the RAG1 NTR regulates V(D)J recombination and lymphocyte development by several mechanisms, including a multifaceted control of the balance between short- and long-range recombination.
ISBN: 9798522948207Subjects--Topical Terms:
611031
Immunology.
Subjects--Index Terms:
Lymphocyte development
The Role of the RAG1 Non-Core Domain in V(D)J Recombination and Lymphocyte Development.
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Immunoglobulin and T cell receptor gene assembly depend on V(D)J recombination initiated by the RAG1-RAG2 recombinase. The RAG1 N-terminal region (NTR; aa 1-383) has been implicated in regulatory functions whose influence on V(D)J recombination and lymphocyte development in vivo are poorly understood. We generated mouse strains in which RAG1 lacks its first 215 residues (Δ215), E3 ubiquitin ligase activity (P326G), or the major site of autoubiquitination (K233R). RAG1 protein levels are increased in all three mutants and RAG1-P326G B cells exhibit increased cell death during development and an increased lgK:lgλ ratio. Previous studies have demonstrated that recombination of the immunoglobulin heavy chain gene (Igh) occurs by two distinct reaction modes: long-range, cohesin-dependent scanning and short-range collision. We find that RAG1Δ215 mice exhibit reduced short-range Igh D-to-J recombination. In addition, we find the V gene segment repertoire is altered in RAG1Δ215 mice at the Igh and IgK loci, while loss of integrity of the E3 ubiquitin ligase domain leads to a decrease in out-of-frame recombination events at the Igh locus.We also demonstrate preliminary findings indicating that off-target recombination events may also be dictated by the same mechanisms of short- and long-range recombination. Our findings indicate that the RAG1 NTR regulates V(D)J recombination and lymphocyte development by several mechanisms, including a multifaceted control of the balance between short- and long-range recombination.
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https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28315434
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