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哺乳动物θ1珠蛋白启动子独特的序列组织及红系细胞特异性核因子结合

Unique sequence organization and erythroid cell-specific nuclear factor-binding of mammalian theta 1 globin promoters.

作者信息

Kim J H, Yu C Y, Bailey A, Hardison R, Shen C K

机构信息

Department of Genetics, University of California, Davis 95616.

出版信息

Nucleic Acids Res. 1989 Jul 25;17(14):5687-700. doi: 10.1093/nar/17.14.5687.

Abstract

The theta 1 globin gene is an alpha globin-like gene, and started to diverge from the other members of the alpha globin family 260 million years ago. DNA sequencing and transcriptional analysis indicated that it is functional in erythroid cells of the higher primates, but not in prosimians and rabbit. The theta 1 promoter region of higher primates including man consists of GC-rich sequences characteristic of housekeeping gene promoters, and CCAAT and TATA boxes located further upstream. It is shown here that the housekeeping gene promoter-like region of human theta 1 contains two tandemly arranged, GC-rich motifs (GC-I and GC-II). Of these, GC-II interacts with nuclear factor(s) present in the globin-expressing, erythroleukemia cell line K562, before and after hemin induction. GC-I, however, interacts with nuclear factor(s) only present in hemin-induced K562 cells. These factors are different from previously reported erythroid cell-specific factors, and are not detectable in non-erythroid Hela cells. Furthermore, the sequence of the motif GC-I and its location relative to ATG codon have been conserved among all known mammalian theta 1 globin genes. Finally, and most interestingly, the CCAAT box of theta 1 is contained within a 38 bp internal segment of Alu repeat sequence. Immediately upstream from this CCAAT box-containing Alu repeat segment is a 241 bp Alu repeat pointing in the opposite direction. The conservation of this novel arrangement among the higher primates suggests that an inserted Alu family repeat and its flanking genomic sequence have co-evolved, for at least 30 million years, to provide the canonical CCAAT and TATA promoter elements of the theta 1 globin genes in higher primates.

摘要

θ1珠蛋白基因是一种α珠蛋白样基因,于2.6亿年前开始与α珠蛋白家族的其他成员分化。DNA测序和转录分析表明,它在高等灵长类动物的红细胞中具有功能,但在原猴和兔子中则没有。包括人类在内的高等灵长类动物的θ1启动子区域由管家基因启动子特有的富含GC的序列以及位于更上游的CCAAT和TATA框组成。本文表明,人类θ1的管家基因启动子样区域包含两个串联排列的富含GC的基序(GC-I和GC-II)。其中,GC-II在血红素诱导前后与表达珠蛋白的红白血病细胞系K562中存在的核因子相互作用。然而,GC-I仅与血红素诱导的K562细胞中存在的核因子相互作用。这些因子不同于先前报道的红细胞特异性因子,在非红细胞的Hela细胞中无法检测到。此外,基序GC-I的序列及其相对于ATG密码子的位置在所有已知的哺乳动物θ1珠蛋白基因中都得到了保守。最后,也是最有趣的是,θ1的CCAAT框包含在Alu重复序列的一个38 bp内部片段中。在这个包含CCAAT框的Alu重复片段的紧上游是一个方向相反的241 bp Alu重复序列。这种新排列在高等灵长类动物中的保守性表明,一个插入的Alu家族重复序列及其侧翼基因组序列至少共同进化了3000万年,以提供高等灵长类动物中θ1珠蛋白基因的典型CCAAT和TATA启动子元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d3/318189/68b9f0b0a3da/nar00131-0272-a.jpg

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