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由Blm缺陷导致的基因组不稳定会损害B细胞谱系的发育、维持和功能。

Genomic instability resulting from Blm deficiency compromises development, maintenance, and function of the B cell lineage.

作者信息

Babbe Holger, McMenamin Jennifer, Hobeika Elias, Wang Jing, Rodig Scott J, Reth Michael, Leder Philip

机构信息

Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Immunol. 2009 Jan 1;182(1):347-60. doi: 10.4049/jimmunol.182.1.347.

Abstract

The RecQ family helicase BLM is critically involved in the maintenance of genomic stability, and BLM mutation causes the heritable disorder Bloom's syndrome. Affected individuals suffer from a predisposition to a multitude of cancer types and an ill-defined immunodeficiency involving low serum Ab titers. To investigate its role in B cell biology, we inactivated murine Blm specifically in B lymphocytes in vivo. Numbers of developing B lymphoid cells in the bone marrow and mature B cells in the periphery were drastically reduced upon Blm inactivation. Of the major peripheral B cell subsets, B1a cells were most prominently affected. In the sera of Blm-deficient naive mice, concentrations of all Ig isotypes were low, particularly IgG3. Specific IgG Ab responses upon immunization were poor and mutant B cells exhibited a generally reduced Ab class switch capacity in vitro. We did not find evidence for a crucial role of Blm in the mechanism of class switch recombination. However, a modest shift toward microhomology-mediated switch junction formation was observed in Blm-deficient B cells. Finally, a cohort of p53-deficient, conditional Blm knockout mice revealed an increased propensity for B cell lymphoma development. Impaired cell cycle progression and survival as well as high rates of chromosomal structural abnormalities in mutant B cell blasts were identified as the basis for the observed effects. Collectively, our data highlight the importance of BLM-dependent genome surveillance for B cell immunity by ensuring proper development and function of the various B cell subsets while counteracting lymphomagenesis.

摘要

RecQ家族解旋酶BLM在维持基因组稳定性方面起着关键作用,BLM突变会导致遗传性疾病布卢姆综合征。患者易患多种癌症类型,并伴有血清抗体滴度低的不明免疫缺陷。为了研究其在B细胞生物学中的作用,我们在体内特异性地使小鼠B淋巴细胞中的Blm失活。Blm失活后,骨髓中发育中的B淋巴细胞数量和外周成熟B细胞数量急剧减少。在外周主要的B细胞亚群中,B1a细胞受影响最为显著。在Blm缺陷的未免疫小鼠血清中,所有Ig同种型的浓度都很低,尤其是IgG3。免疫后的特异性IgG抗体反应较差,突变B细胞在体外的抗体类别转换能力普遍降低。我们没有发现Blm在类别转换重组机制中起关键作用的证据。然而,在Blm缺陷的B细胞中观察到向微同源性介导的转换连接形成有适度转变。最后,一组p53缺陷的条件性Blm基因敲除小鼠显示出B细胞淋巴瘤发生的倾向增加。突变B细胞母细胞中细胞周期进程和存活受损以及染色体结构异常率高被确定为观察到的效应的基础。总体而言,我们的数据通过确保各种B细胞亚群的正常发育和功能,同时对抗淋巴瘤发生,突出了BLM依赖性基因组监测对B细胞免疫的重要性。

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本文引用的文献

2
Molecular genetics of RecQ helicase disorders.
Cell Mol Life Sci. 2007 Sep;64(17):2306-22. doi: 10.1007/s00018-007-7121-z.
3
The Bloom's syndrome helicase is critical for development and function of the alphabeta T-cell lineage.
Mol Cell Biol. 2007 Mar;27(5):1947-59. doi: 10.1128/MCB.01402-06. Epub 2007 Jan 8.
4
Testing gene function early in the B cell lineage in mb1-cre mice.
Proc Natl Acad Sci U S A. 2006 Sep 12;103(37):13789-94. doi: 10.1073/pnas.0605944103. Epub 2006 Aug 29.
5
Mutation of the murine Bloom's syndrome gene produces global genome destabilization.
Mol Cell Biol. 2006 Sep;26(17):6713-26. doi: 10.1128/MCB.00296-06.
6
The Bloom's syndrome helicase can promote the regression of a model replication fork.
J Biol Chem. 2006 Aug 11;281(32):22839-46. doi: 10.1074/jbc.M604268200. Epub 2006 Jun 8.
7
H2AX prevents DNA breaks from progressing to chromosome breaks and translocations.
Mol Cell. 2006 Jan 20;21(2):201-14. doi: 10.1016/j.molcel.2006.01.005.
8
Redundancy of DNA helicases in p53-mediated apoptosis.
Oncogene. 2006 Mar 30;25(14):2119-23. doi: 10.1038/sj.onc.1209242.
9
Maintenance of serum antibody levels.
Annu Rev Immunol. 2005;23:367-86. doi: 10.1146/annurev.immunol.23.021704.115723.
10
Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion.
Springer Semin Immunopathol. 2005 Mar;26(4):347-62. doi: 10.1007/s00281-004-0182-2. Epub 2005 Jan 5.

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