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在依赖染色体转移至二倍体小鼠红白血病细胞后,人类α珠蛋白基因复合物内的选择性表达。

Selective expression within the human alpha globin gene complex following chromosome-dependent transfer into diploid mouse erythroleukaemia cells.

作者信息

Zeitlin H C, Weatherall D J

出版信息

Mol Biol Med. 1983 Dec;1(5):489-500.

PMID:6594559
Abstract

Human chromosome 16, which contains the alpha globin gene complex, has been introduced into mouse erythroleukaemia cells by means of cell fusion and selectively retained to the exclusion of other human chromosomes. After induction of haemoglobin synthesis in hybrid clones, evidence for expression of the human alpha globin genes was sought by mRNA and globin chain synthesis analyses. It was found that both the human alpha 1 and alpha 2 genes were similarly expressed and that the synthesis of human alpha globin chains was nearly half that of mouse alpha chains on a per gene basis. The pattern of human alpha gene expression was similar with different inducers and with donor chromosomes of either erythroid or non-erythroid origin. However, the closely linked human embryonic alpha gene (zeta) did not produce detectable levels of zeta globin mRNA in any of the hybrid clones. Thus, there is selective activation of adult genes in the human alpha globin gene complex in the mouse erythroleukaemia cell.

摘要

包含α珠蛋白基因复合体的人类16号染色体,已通过细胞融合的方式导入小鼠红白血病细胞,并被选择性保留,而排除了其他人类染色体。在杂交克隆中诱导血红蛋白合成后,通过mRNA和珠蛋白链合成分析来寻找人类α珠蛋白基因表达的证据。结果发现,人类α1和α2基因的表达相似,并且在每个基因的基础上,人类α珠蛋白链的合成量几乎是小鼠α链的一半。不同诱导剂以及来源于红系或非红系的供体染色体,人类α基因的表达模式相似。然而,紧密连锁的人类胚胎α基因(ζ)在任何杂交克隆中都未产生可检测水平的ζ珠蛋白mRNA。因此,在小鼠红白血病细胞中,人类α珠蛋白基因复合体中的成人基因存在选择性激活。

相似文献

1
Selective expression within the human alpha globin gene complex following chromosome-dependent transfer into diploid mouse erythroleukaemia cells.在依赖染色体转移至二倍体小鼠红白血病细胞后,人类α珠蛋白基因复合物内的选择性表达。
Mol Biol Med. 1983 Dec;1(5):489-500.
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Inducible expression of a neo gene integrated into the human alpha-globin gene cluster.整合到人α-珠蛋白基因簇中的新霉素基因的诱导表达。
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Globin gene expression in somatic cell hybrids.体细胞杂种中的珠蛋白基因表达。
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Expression of human alpha-globin genes in hybrid mouse erythroleukaemia cells depends on differentiated state of human donor cell.人α-珠蛋白基因在杂交小鼠红白血病细胞中的表达取决于人供体细胞的分化状态。
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引用本文的文献

1
ATR-16 syndrome: mechanisms linking monosomy to phenotype.ATR-16 综合征:单体型与表型相关联的机制。
J Med Genet. 2020 Jun;57(6):414-421. doi: 10.1136/jmedgenet-2019-106528. Epub 2020 Jan 31.
2
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).α地中海贫血/智力发育迟缓综合征(ATR-16)中16号染色体短臂的从头截断及(TTAGGG)n修复。
Am J Hum Genet. 1993 Apr;52(4):668-76.
3
Healing of broken human chromosomes by the addition of telomeric repeats.通过添加端粒重复序列修复断裂的人类染色体。
Am J Hum Genet. 1994 Sep;55(3):505-12.
4
S1 nuclease analysis of alpha-globin gene expression in preleukemic patients with acquired hemoglobin H disease after transfer to mouse erythroleukemia cells.对转至小鼠红白血病细胞后患有获得性血红蛋白H病的白血病前期患者α-珠蛋白基因表达的S1核酸酶分析
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2387-90. doi: 10.1073/pnas.84.8.2387.
5
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.α地中海贫血/智力发育迟缓综合征的临床特征与分子分析。II. α珠蛋白复合体无可检测异常的病例。
Am J Hum Genet. 1990 Jun;46(6):1127-40.
6
The LCR-like alpha-globin positive regulatory element functions as an enhancer in transiently transfected cells during erythroid differentiation.类LCR的α-珠蛋白阳性调控元件在红系分化过程中,在瞬时转染细胞中作为增强子发挥作用。
Nucleic Acids Res. 1992 Jan 25;20(2):237-43. doi: 10.1093/nar/20.2.237.
7
In vivo footprinting of the human alpha-globin locus upstream regulatory element by guanine and adenine ligation-mediated polymerase chain reaction.通过鸟嘌呤和腺嘌呤连接介导的聚合酶链反应对人α-珠蛋白基因座上游调控元件进行体内足迹分析。
Mol Cell Biol. 1992 May;12(5):2135-42. doi: 10.1128/mcb.12.5.2135-2142.1992.