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1
gamma Heavy chain disease in man: cDNA sequence supports partial gene deletion model.人类γ重链病:cDNA序列支持部分基因缺失模型。
Proc Natl Acad Sci U S A. 1982 May;79(10):3260-4. doi: 10.1073/pnas.79.10.3260.
2
Gamma heavy chain disease in man. Genomic sequence reveals two noncontiguous deletions in a single gene.人类γ重链病。基因组序列揭示单个基因中的两个非连续缺失。
J Clin Invest. 1988 Oct;82(4):1244-52. doi: 10.1172/JCI113722.
3
Multiple genomic defects result in an alternative RNA splice creating a human gamma H chain disease protein.多种基因组缺陷导致一种替代RNA剪接,产生一种人类γ重链病蛋白。
J Immunol. 1988 Sep 1;141(5):1762-8.
4
Genomic alterations in a case of alpha heavy chain disease leading to the generation of composite exons from the JH region.一例α重链病中的基因组改变导致从JH区域产生复合外显子。
Eur J Immunol. 1989 Nov;19(11):2093-8. doi: 10.1002/eji.1830191119.
5
Human heavy chain disease protein WIS: implications for the organization of immunoglobulin genes.人类重链病蛋白WIS:对免疫球蛋白基因组织的影响
Proc Natl Acad Sci U S A. 1979 Jan;76(1):452-6. doi: 10.1073/pnas.76.1.452.
6
Articular, monoclonal gamma3 heavy-chain deposition disease: characterization of a partially deleted heavy-chain gene and its protein product synthesized in vivo and in vitro.关节型单克隆γ3重链沉积病:体内外合成的部分缺失重链基因及其蛋白产物的特征
Arthritis Rheum. 2003 Nov;48(11):3266-71. doi: 10.1002/art.11298.
7
Gamma heavy chain disease in man: independent structural abnormalities and reduced transcription of a functionally rearranged lambda L-chain gene result in the absence of L-chains.人类γ重链病:功能重排的λ轻链基因存在独立的结构异常且转录减少,导致轻链缺失。
Blood Cells Mol Dis. 2000 Jun;26(3):177-85. doi: 10.1006/bcmd.2000.0294.
8
The productive gene for alpha-H chain disease protein MAL is highly modified by insertion-deletion processes.α-H链病蛋白MAL的产生性基因通过插入-缺失过程被高度修饰。
J Immunol. 1989 Dec 1;143(11):3821-7.
9
Correlation between fragmented immunoglobulin genes and heavy chain deletion mutants.片段化免疫球蛋白基因与重链缺失突变体之间的相关性。
Nature. 1979 Oct 18;281(5732):600-2. doi: 10.1038/281600a0.
10
Gene mutations and alternate RNA splicing result in truncated Ig L chains in human gamma H chain disease.基因突变和替代性RNA剪接导致人类γ重链病中截短的Ig轻链。
J Immunol. 1988 Sep 1;141(5):1738-44.

引用本文的文献

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Recombinant antibodies and their use for food immunoanalysis.重组抗体及其在食品免疫分析中的应用。
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Camelid Single-Domain Antibodies: Historical Perspective and Future Outlook.骆驼科单域抗体:历史回顾与未来展望
Front Immunol. 2017 Nov 20;8:1589. doi: 10.3389/fimmu.2017.01589. eCollection 2017.
3
Resolving the micro-heterogeneity and structural integrity of monoclonal antibodies by hybrid mass spectrometric approaches.通过混合质谱方法解析单克隆抗体的微观异质性和结构完整性
MAbs. 2017 May/Jun;9(4):638-645. doi: 10.1080/19420862.2017.1290033. Epub 2017 Feb 14.
4
Heavy chain-only antibodies are spontaneously produced in light chain-deficient mice.仅重链抗体在轻链缺陷小鼠中自发产生。
J Exp Med. 2007 Dec 24;204(13):3271-83. doi: 10.1084/jem.20071155. Epub 2007 Dec 17.
5
Heavy-chain only antibodies derived from dromedary are secreted and displayed by mouse B cells.源自单峰骆驼的仅重链抗体由小鼠B细胞分泌并展示。
Immunology. 2003 May;109(1):93-101. doi: 10.1046/j.1365-2567.2003.01633.x.
6
Translocation of immunoglobulin VH genes in Burkitt lymphoma.伯基特淋巴瘤中免疫球蛋白VH基因的易位
Proc Natl Acad Sci U S A. 1982 Sep;79(18):5611-5. doi: 10.1073/pnas.79.18.5611.
7
Transcriptional activation of the translocated c-myc oncogene in burkitt lymphoma.伯基特淋巴瘤中易位的c-myc癌基因的转录激活
Proc Natl Acad Sci U S A. 1983 Feb;80(3):820-4. doi: 10.1073/pnas.80.3.820.
8
Evolution of B-cell malignancy: pre-B-cell leukemia resulting from MYC activation in a B-cell neoplasm with a rearranged BCL2 gene.B细胞恶性肿瘤的演变:在具有重排BCL2基因的B细胞肿瘤中,MYC激活导致前B细胞白血病。
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8548-52. doi: 10.1073/pnas.85.22.8548.
9
Gamma heavy chain disease in man. Genomic sequence reveals two noncontiguous deletions in a single gene.人类γ重链病。基因组序列揭示单个基因中的两个非连续缺失。
J Clin Invest. 1988 Oct;82(4):1244-52. doi: 10.1172/JCI113722.
10
The t(8;14) breakpoint of the EW 36 undifferentiated lymphoma cell line lies 5' of MYC in a region prone to involvement in endemic Burkitt's lymphomas.EW 36未分化淋巴瘤细胞系的t(8;14)断点位于MYC基因5'端,该区域易发生地方性伯基特淋巴瘤。
Nucleic Acids Res. 1988 Mar 25;16(5):2077-85. doi: 10.1093/nar/16.5.2077.

本文引用的文献

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Size heterogeneity in the 3' end of dihydrofolate reductase messenger RNAs in mouse cells.小鼠细胞中二氢叶酸还原酶信使核糖核酸3'端的大小异质性
Cell. 1980 Nov;22(2 Pt 2):361-70. doi: 10.1016/0092-8674(80)90346-3.
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Mechanisms for the incorporation of proteins in membranes and organelles.蛋白质整合到膜和细胞器中的机制。
J Cell Biol. 1982 Jan;92(1):1-22. doi: 10.1083/jcb.92.1.1.
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Plasmid screening at high colony density.高菌落密度下的质粒筛选
Gene. 1980 Jun;10(1):63-7. doi: 10.1016/0378-1119(80)90144-4.
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Structural studies of a human gamma 3 myeloma protein (Goe) that binds staph protein A.一种结合葡萄球菌蛋白A的人类γ3骨髓瘤蛋白(Goe)的结构研究。
J Immunol. 1981 Sep;127(3):917-23.
5
Comparison of mouse immunoglobulin gamma 2a and gamma 2b chain genes suggests that exons can be exchanged between genes in a multigenic family.小鼠免疫球蛋白γ2a和γ2b链基因的比较表明,外显子可在多基因家族的基因之间进行交换。
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2442-6. doi: 10.1073/pnas.78.4.2442.
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Three cDNA clones encoding mouse transplantation antigens: homology to immunoglobulin genes.三个编码小鼠移植抗原的cDNA克隆:与免疫球蛋白基因的同源性
Cell. 1981 Apr;24(1):125-34. doi: 10.1016/0092-8674(81)90508-0.
7
Structure of the constant and 3' untranslated regions of the murine Balb/c gamma 2a heavy chain messenger RNA.小鼠Balb/cγ2a重链信使核糖核酸的恒定区和3'非翻译区的结构
Nucleic Acids Res. 1980 Jul 25;8(14):3143-55. doi: 10.1093/nar/8.14.3143.
8
A mouse immunoglobulin heavy chain deletion mutant: isolation of a cDNA clone and sequence analysis of the mRNA.一种小鼠免疫球蛋白重链缺失突变体:cDNA克隆的分离及mRNA的序列分析
Nucleic Acids Res. 1980 Apr 11;8(7):1475-84. doi: 10.1093/nar/8.7.1475.
9
Primary structure of human gamma 3 immunoglobulin deletion mutant: gamma 3 heavy-chain disease protein Wis.人γ3免疫球蛋白缺失突变体的一级结构:γ3重链病蛋白Wis
Biochemistry. 1980 Sep 2;19(18):4304-8. doi: 10.1021/bi00559a024.
10
An immunoglobulin deletion mutant with implications for the heavy-chain switch and RNA splicing.一种对重链转换和RNA剪接有影响的免疫球蛋白缺失突变体。
Nature. 1980 Aug 14;286(5774):669-75. doi: 10.1038/286669a0.

人类γ重链病:cDNA序列支持部分基因缺失模型。

gamma Heavy chain disease in man: cDNA sequence supports partial gene deletion model.

作者信息

Alexander A, Steinmetz M, Barritault D, Frangione B, Franklin E C, Hood L, Buxbaum J N

出版信息

Proc Natl Acad Sci U S A. 1982 May;79(10):3260-4. doi: 10.1073/pnas.79.10.3260.

DOI:10.1073/pnas.79.10.3260
PMID:6808505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC346395/
Abstract

Human gamma heavy chain disease (HCD) is characterized by the presence in serum of a short monoclonal Ig gamma chain unattached to light chains. Although most HCD proteins have internal deletions, in some the defect is NH2-terminal. The OMM gamma 3 HCD serum protein is of the latter type, having undergone an extensive NH2-terminal deletion with a sequence starting within the hinge. A cell line synthesizing the OMM protein has enabled us to study the biogenesis of the abnormal molecule. In vitro translation of isolated mRNA yields a protein containing a hydrophobic NH2-terminal leader sequence. In the intact cell, the precursor molecule is processed normally to yield a protein with an NH2-terminal sequence homologous to the beginning of the variable (V) region. The nucleotide sequence of cDNA prepared from the OMM mRNA encodes a 19-amino acid leader followed by the first 15 residues of the V region. An extensive internal deletion encompasses the remainder of the V and the entire CH1 domain. Immediately following the short V region, there is information in the cDNA for the entire normal hinge. The primary synthetic product is thus an internally deleted molecule that undergoes postsynthetic degradation to yield the NH2-terminally deleted serum protein. The structure of the OMM mRNA suggests that the protein abnormality results from a partial gene deletion rather than defective splicing.

摘要

人类γ重链病(HCD)的特征是血清中存在未与轻链相连的短单克隆Igγ链。尽管大多数HCD蛋白存在内部缺失,但在某些情况下,缺陷位于氨基末端。OMMγ3 HCD血清蛋白属于后一种类型,其氨基末端发生了广泛缺失,序列起始于铰链区。一个合成OMM蛋白的细胞系使我们能够研究这种异常分子的生物发生。分离的mRNA的体外翻译产生一种含有疏水氨基末端前导序列的蛋白质。在完整细胞中,前体分子正常加工,产生一种氨基末端序列与可变(V)区起始部分同源的蛋白质。从OMM mRNA制备的cDNA的核苷酸序列编码一个19个氨基酸的前导序列,随后是V区的前15个残基。广泛的内部缺失涵盖了V区的其余部分和整个CH1结构域。紧随短V区之后,cDNA中有整个正常铰链区的信息。因此,主要合成产物是一个内部缺失的分子,它经历合成后降解,产生氨基末端缺失的血清蛋白。OMM mRNA的结构表明,蛋白质异常是由部分基因缺失而非剪接缺陷导致的。