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人类θ1-珠蛋白基因在胚胎/胎儿及成人红细胞中的发育性和诱导性表达模式。

Developmental and inducible patterns of human theta 1-globin gene expression in embryonic/fetal and adult erythroid cells.

作者信息

Mamalaki A, Anagnou N P, Moschonas N K

机构信息

Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Crete, Greece.

出版信息

Am J Hematol. 1990 Dec;35(4):251-7. doi: 10.1002/ajh.2830350406.

DOI:10.1002/ajh.2830350406
PMID:2239920
Abstract

Human theta (theta 1)-globin gene represents a member of the alpha-like globin gene family residing on chromosome 16. theta 1-Specific transcripts have been detected so far only in erythroid tissues and in erythroleukemia K562 cells. To investigate systematically its inducible expression and developmental specificity, we analyzed at the RNA level five additional human erythroleukemia cell lines with diverse developmental globin programs, two somatic cell hybrids between K562 and mouse erythroleukemia (MEL) cells, a human fetal liver x MEL somatic cell hybrid, and reticulocytes and bone marrow cells from normal adults. theta 1-Globin gene was expressed in all cell types. Inducible expression (two- to sixfold) was documented both in HEL and K562 erythroleukemia cells after 5-azacytidine treatment. Like K562 cells, HEL cells also displayed hemin-inducible theta 1-globin gene expression. Following transfer of human chromosome 16 from embryonic/fetal K562 to the adult MEL cells, theta 1-globin gene remained active but lost its potential for inducibility, suggesting probably a trans regulation mechanism. Higher levels of theta 1 mRNA were found in fetal liver cells compared with trace amounts in reticulocytes and normal adult bone marrow cells. These data clearly show that in contrast to the embryonic and adult patterns of expression of zeta and alpha-globin genes, respectively, theta 1-globin gene displays a different profile, being active predominantly during the early stages of ontogeny, switching to lower levels of expression in adulthood.

摘要

人θ(θ1)-珠蛋白基因是位于16号染色体上的α-类珠蛋白基因家族的成员。到目前为止,仅在红系组织和红白血病K562细胞中检测到θ1特异性转录本。为了系统地研究其诱导表达和发育特异性,我们在RNA水平分析了另外五种具有不同发育珠蛋白程序的人红白血病细胞系、K562与小鼠红白血病(MEL)细胞之间的两种体细胞杂种、人胎儿肝脏×MEL体细胞杂种以及正常成年人的网织红细胞和骨髓细胞。θ1-珠蛋白基因在所有细胞类型中均有表达。5-氮杂胞苷处理后,HEL和K562红白血病细胞中均记录到诱导表达(2至6倍)。与K562细胞一样,HEL细胞也表现出血红素诱导的θ1-珠蛋白基因表达。将人16号染色体从胚胎/胎儿K562转移到成年MEL细胞后,θ1-珠蛋白基因仍然活跃,但失去了诱导潜力,这可能暗示了一种反式调节机制。与网织红细胞和正常成年骨髓细胞中的微量相比,胎儿肝细胞中发现了更高水平的θ1 mRNA。这些数据清楚地表明,与ζ和α-珠蛋白基因分别在胚胎期和成年期的表达模式不同,θ1-珠蛋白基因表现出不同的特征,主要在个体发育的早期阶段活跃,在成年期转变为较低水平的表达。

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1
Developmental and inducible patterns of human theta 1-globin gene expression in embryonic/fetal and adult erythroid cells.人类θ1-珠蛋白基因在胚胎/胎儿及成人红细胞中的发育性和诱导性表达模式。
Am J Hematol. 1990 Dec;35(4):251-7. doi: 10.1002/ajh.2830350406.
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