• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
BCL8, a novel gene involved in translocations affecting band 15q11-13 in diffuse large-cell lymphoma.BCL8,一种与弥漫性大细胞淋巴瘤中影响15q11 - 13带的易位相关的新基因。
Proc Natl Acad Sci U S A. 1997 May 27;94(11):5728-32. doi: 10.1073/pnas.94.11.5728.
2
Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21.易位t(1;14)(q21;q32)的分子克隆确定了位于1号染色体q21的一个新基因(BCL9)。
Blood. 1998 Mar 15;91(6):1873-81.
3
Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas.B细胞淋巴瘤中与复发性染色体易位t(3;14)(q27;q32)和t(3;22)(q27;q11)相关基因的鉴定。
Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5262-6. doi: 10.1073/pnas.90.11.5262.
4
The t(9;14)(p13;q32) chromosomal translocation associated with lymphoplasmacytoid lymphoma involves the PAX-5 gene.与淋巴浆细胞样淋巴瘤相关的t(9;14)(p13;q32)染色体易位涉及PAX-5基因。
Blood. 1996 Dec 1;88(11):4110-7.
5
MYC rearrangement and translocations involving band 8q24 in diffuse large cell lymphomas.弥漫性大细胞淋巴瘤中涉及8q24带的MYC重排和易位。
Blood. 1991 Mar 1;77(5):1057-63.
6
Molecular and clinical features of non-Burkitt's, diffuse large-cell lymphoma of B-cell type associated with the c-MYC/immunoglobulin heavy-chain fusion gene.与c-MYC/免疫球蛋白重链融合基因相关的B细胞型非伯基特弥漫大细胞淋巴瘤的分子和临床特征
J Clin Oncol. 2000 Feb;18(3):510-18. doi: 10.1200/JCO.2000.18.3.510.
7
Establishment of a human cell line (SKI-DLCL-1) with a t(1;14)(q21;q32) translocation from the ascites of a patient with diffuse large cell lymphoma.从一名弥漫性大B细胞淋巴瘤患者的腹水中建立携带t(1;14)(q21;q32)易位的人细胞系(SKI-DLCL-1)。
Leuk Lymphoma. 2001 Jan;40(3-4):419-23. doi: 10.3109/10428190109057942.
8
Polymerase chain reaction detection of cells carrying t(14;18) in bone marrow of patients with follicular and diffuse large B-cell lymphoma: the importance of analysis at diagnosis and significance of long-term follow-up.聚合酶链反应检测滤泡性和弥漫性大B细胞淋巴瘤患者骨髓中携带t(14;18)的细胞:诊断时分析的重要性及长期随访的意义
Neoplasma. 2001;48(6):501-5.
9
BCL8 is a novel, evolutionarily conserved human gene family encoding proteins with presumptive protein kinase A anchoring function.BCL8是一个新的、进化上保守的人类基因家族,其编码的蛋白质具有假定的蛋白激酶A锚定功能。
Genomics. 2002 Aug;80(2):158-65. doi: 10.1006/geno.2002.6822.
10
Involvement of the chromosomal translocation t(11;18) in some mucosa-associated lymphoid tissue lymphomas and diffuse large B-cell lymphomas of the ocular adnexa: evidence from multiplex reverse transcriptase-polymerase chain reaction and fluorescence in situ hybridization on using formalin-fixed, paraffin-embedded specimens.染色体易位t(11;18)在某些黏膜相关淋巴组织淋巴瘤及眼附属器弥漫性大B细胞淋巴瘤中的作用:来自对福尔马林固定、石蜡包埋标本进行多重逆转录聚合酶链反应和荧光原位杂交的证据
Mod Pathol. 2003 May;16(5):445-52. doi: 10.1097/01.MP.0000067421.92575.6E.

引用本文的文献

1
Identification of gene pairs through penalized regression subject to constraints.通过受约束的惩罚回归识别基因对。
BMC Bioinformatics. 2017 Nov 3;18(1):466. doi: 10.1186/s12859-017-1872-9.
2
Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers.全基因组和转录组测序的综合分析揭示了肝癌中由体细胞基因组变化驱动的多种转录组异常。
PLoS One. 2014 Dec 19;9(12):e114263. doi: 10.1371/journal.pone.0114263. eCollection 2014.
3
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.15号染色体着丝粒周围区域的组织:在15q近端重复的患者中,至少有四个部分基因拷贝被扩增。
J Med Genet. 2002 Mar;39(3):170-7. doi: 10.1136/jmg.39.3.170.
4
Molecular diagnostic approach to non-Hodgkin's lymphoma.非霍奇金淋巴瘤的分子诊断方法
J Mol Diagn. 2000 Nov;2(4):178-90. doi: 10.1016/S1525-1578(10)60636-8.
5
Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.普拉德-威利综合征和安吉尔曼综合征缺失区域新型印记转录本的鉴定:区域印记控制的进一步证据。
Am J Hum Genet. 2000 Mar;66(3):848-58. doi: 10.1086/302817.
6
Frequent occurrence of deletions and duplications during somatic hypermutation: implications for oncogene translocations and heavy chain disease.体细胞高频突变过程中缺失和重复的频繁发生:对癌基因易位和重链病的影响
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2463-8. doi: 10.1073/pnas.95.5.2463.
7
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.15号染色体15q11 - q13上普拉德-威利/安吉尔曼区域的整合酵母人工染色体(YAC)重叠群图谱,平均序列标签位点(STS)间距为35千碱基对(kb)。
Genome Res. 1998 Feb;8(2):146-57. doi: 10.1101/gr.8.2.146.

本文引用的文献

1
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.人类15号染色体上的印记转换可能涉及小核核糖核蛋白多肽N(SNRPN)基因的可变转录本。
Nat Genet. 1996 Oct;14(2):163-70. doi: 10.1038/ng1096-163.
2
Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis.人类单亲二体:印记图谱的发展及其对产前诊断的意义。
Hum Mol Genet. 1995;4 Spec No:1757-64. doi: 10.1093/hmg/4.suppl_1.1757.
3
Subregional localization of 20 single-copy loci to chromosome 6 by fluorescence in situ hybridization.通过荧光原位杂交将20个单拷贝基因座亚定位到6号染色体上。
Genomics. 1993 May;16(2):426-30. doi: 10.1006/geno.1993.1206.
4
Rearrangement of the bcl-6 gene as a prognostic marker in diffuse large-cell lymphoma.bcl-6基因重排作为弥漫性大细胞淋巴瘤的预后标志物
N Engl J Med. 1994 Jul 14;331(2):74-80. doi: 10.1056/NEJM199407143310202.
5
Chromosomal translocations in human cancer.人类癌症中的染色体易位
Nature. 1994 Nov 10;372(6502):143-9. doi: 10.1038/372143a0.
6
Human immunoglobulin VH and D segments on chromosomes 15q11.2 and 16p11.2.位于15号染色体q11.2区域和16号染色体p11.2区域上的人类免疫球蛋白VH和D基因片段。
Hum Mol Genet. 1994 Jun;3(6):853-60. doi: 10.1093/hmg/3.6.853.
7
Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locus.主要IGH基因座之外的人类免疫球蛋白重链可变基因片段的定位
Genomics. 1994 Sep 1;23(1):151-7. doi: 10.1006/geno.1994.1471.
8
BCL-6 and the molecular pathogenesis of B-cell lymphoma.BCL-6与B细胞淋巴瘤的分子发病机制
Cold Spring Harb Symp Quant Biol. 1994;59:117-23. doi: 10.1101/sqb.1994.059.01.015.
9
The Non-Hodgkin Lymphoma Pathologic Classification Project. Long-term follow-up of 1153 patients with non-Hodgkin lymphomas.非霍奇金淋巴瘤病理分类项目。1153例非霍奇金淋巴瘤患者的长期随访
Ann Intern Med. 1988 Dec 15;109(12):939-45. doi: 10.7326/0003-4819-109-12-939.
10
Dispersed localization of D segments in the human immunoglobulin heavy-chain locus.人类免疫球蛋白重链基因座中D片段的分散定位。
EMBO J. 1988 Apr;7(4):1047-51. doi: 10.1002/j.1460-2075.1988.tb02912.x.

BCL8,一种与弥漫性大细胞淋巴瘤中影响15q11 - 13带的易位相关的新基因。

BCL8, a novel gene involved in translocations affecting band 15q11-13 in diffuse large-cell lymphoma.

作者信息

Dyomin V G, Rao P H, Dalla-Favera R, Chaganti R S

机构信息

Cell Biology Program and the Department of Human Genetics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 May 27;94(11):5728-32. doi: 10.1073/pnas.94.11.5728.

DOI:10.1073/pnas.94.11.5728
PMID:9159141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC20847/
Abstract

Translocations affecting the chromosomal region 15q11-13 and various other partners are recurrent in diffuse large-cell lymphomas (DLCL). To identify the putative gene, here named BCL8, involved in these translocations we have cloned the breakpoint region from a DLCL patient with t(14;15)(q32;q11-13) and the corresponding germ-line region from chromosome 15. The genomic locus on chromosome 15 is clonally rearranged in about 4% of DLCL in agreement with the frequency of 15q11-13 translocations. A probe derived from the BCL8 locus on chromosome 15 detected a transcript in human testis and prostate, whereas no expression was found in spleen, thymus, and blood leukocytes. Analysis of the BCL8 cDNA clones isolated from human testis cDNA library showed that the BCL8 gene generates a major transcript of 2.6 kb and a less prominent 4.5-kb species due to differential polyadenylylation. By reverse transcription-PCR analysis of RNA extracted from frozen DLCL samples and lymphoma cell lines, BCL8 expression was detected in all patients carrying 15q11-13 abnormalities and in a fraction of randomly selected DLCL patients. These results suggest that the BCL8 gene is not normally expressed in lymphoid tissues, but its expression can be activated by chromosomal translocation or by other mechanisms in DLCL. Ectopic expression of BCL8 in a significant proportion of DLCL suggests an important role for this gene in the molecular pathogenesis of B cell lymphoma.

摘要

影响染色体区域15q11 - 13及其他各种伙伴的易位在弥漫性大细胞淋巴瘤(DLCL)中很常见。为了鉴定参与这些易位的假定基因(此处命名为BCL8),我们从一名患有t(14;15)(q32;q11 - 13)的DLCL患者中克隆了断点区域,并从15号染色体克隆了相应的种系区域。15号染色体上的基因组位点在约4%的DLCL中发生克隆性重排,这与15q11 - 13易位的频率一致。来自15号染色体上BCL8位点的探针在人类睾丸和前列腺中检测到一种转录本,而在脾脏、胸腺和血液白细胞中未发现表达。对从人类睾丸cDNA文库中分离的BCL8 cDNA克隆的分析表明,由于多聚腺苷酸化的差异,BCL8基因产生了一个2.6 kb的主要转录本和一个不太明显的4.5 kb的转录本。通过对从冷冻的DLCL样本和淋巴瘤细胞系中提取的RNA进行逆转录 - PCR分析,在所有携带15q11 - 13异常的患者以及一部分随机选择的DLCL患者中检测到了BCL8表达。这些结果表明,BCL8基因在淋巴组织中通常不表达,但其表达可通过染色体易位或DLCL中的其他机制被激活。BCL8在相当一部分DLCL中的异位表达表明该基因在B细胞淋巴瘤的分子发病机制中起重要作用。