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小鼠组蛋白H2a基因包含一个小元件,该元件有助于无内含子基因转录本和未剪接的HIV-1相关mRNA在细胞质中的积累。

The mouse histone H2a gene contains a small element that facilitates cytoplasmic accumulation of intronless gene transcripts and of unspliced HIV-1-related mRNAs.

作者信息

Huang Y, Carmichael G G

机构信息

Department of Microbiology, University of Connecticut Health Center, Farmington, CT 06030, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10104-9. doi: 10.1073/pnas.94.19.10104.

DOI:10.1073/pnas.94.19.10104
PMID:9294170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC23318/
Abstract

Histone mRNAs are naturally intronless and accumulate efficiently in the cytoplasm. To learn whether there are cis-acting sequences within histone genes that allow efficient cytoplasmic accumulation of RNAs, we made recombinant constructs in which sequences from the mouse H2a gene were cloned into a human beta-globin cDNA. By using transient transfection and RNase protection analysis, we demonstrate here that a 100-bp sequence within the H2a coding region permits efficient cytoplasmic accumulation of the globin cDNA transcripts. We also show that this sequence appears to suppress splicing and can functionally replace Rev and the Rev-responsive element in the cytoplasmic accumulation of unspliced HIV-1-related mRNAs. Like the Rev-responsive element, this sequence acts in an orientation-dependent manner. We thus propose that the sequence identified here may be a member of the cis-acting elements that facilitate the cytoplasmic accumulation of naturally intronless gene transcripts.

摘要

组蛋白mRNA天然无内含子,并在细胞质中高效积累。为了了解组蛋白基因内是否存在允许RNA在细胞质中高效积累的顺式作用序列,我们构建了重组体,其中将小鼠H2a基因的序列克隆到了人β-珠蛋白cDNA中。通过瞬时转染和RNA酶保护分析,我们在此证明H2a编码区内的一段100个碱基对的序列可使珠蛋白cDNA转录本在细胞质中高效积累。我们还表明,该序列似乎能抑制剪接,并且在未剪接的HIV-1相关mRNA的细胞质积累过程中,在功能上可替代Rev和Rev反应元件。与Rev反应元件一样,该序列以方向依赖的方式起作用。因此,我们提出这里鉴定出的序列可能是促进天然无内含子基因转录本在细胞质中积累的顺式作用元件的成员。

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本文引用的文献

1
A suboptimal 5' splice site is a cis-acting determinant of nuclear export of polyomavirus late mRNAs.次优5'剪接位点是多瘤病毒晚期mRNA核输出的顺式作用决定因素。
Mol Cell Biol. 1996 Nov;16(11):6046-54. doi: 10.1128/MCB.16.11.6046.
2
The hepatitis B virus posttranscriptional regulatory element is composed of two subelements.乙肝病毒转录后调控元件由两个子元件组成。
J Virol. 1996 Jul;70(7):4345-51. doi: 10.1128/JVI.70.7.4345-4351.1996.
3
Role of polyadenylation in nucleocytoplasmic transport of mRNA.聚腺苷酸化在mRNA核质转运中的作用。
Mol Cell Biol. 1996 Apr;16(4):1534-42. doi: 10.1128/MCB.16.4.1534.
4
Sequence of the polypyrimidine tract of the 3'-terminal 3' splicing signal can affect intron-dependent pre-mRNA processing in vivo.3'剪接信号3'末端的多嘧啶序列可影响体内内含子依赖性前体mRNA的加工。
Nucleic Acids Res. 1996 May 1;24(9):1765-73. doi: 10.1093/nar/24.9.1765.
5
Identification of a second conserved element within the coding sequence of a mouse H3 histone gene that interacts with nuclear factors and is necessary for normal expression.在小鼠H3组蛋白基因编码序列中鉴定出第二个保守元件,该元件与核因子相互作用,是正常表达所必需的。
Nucleic Acids Res. 1996 Feb 1;24(3):523-31. doi: 10.1093/nar/24.3.523.
6
Polyadenylation site selection cannot occur in vivo after excision of the 3'-terminal intron.3'-末端内含子切除后,聚腺苷酸化位点选择无法在体内发生。
Nucleic Acids Res. 1993 Nov 11;21(22):5256-63. doi: 10.1093/nar/21.22.5256.
7
A novel hepatitis B virus (HBV) genetic element with Rev response element-like properties that is essential for expression of HBV gene products.一种具有类Rev反应元件特性的新型乙型肝炎病毒(HBV)遗传元件,它对于HBV基因产物的表达至关重要。
Mol Cell Biol. 1993 Dec;13(12):7476-86. doi: 10.1128/mcb.13.12.7476-7486.1993.
8
A small element from the Mason-Pfizer monkey virus genome makes human immunodeficiency virus type 1 expression and replication Rev-independent.来自猴泡沫病毒基因组的一个小元件可使1型人类免疫缺陷病毒的表达和复制不依赖于Rev蛋白。
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1256-60. doi: 10.1073/pnas.91.4.1256.
9
Rev and the fate of pre-mRNA in the nucleus: implications for the regulation of RNA processing in eukaryotes.Rev与细胞核内前体mRNA的命运:对真核生物RNA加工调控的影响
Mol Cell Biol. 1993 Oct;13(10):6180-9. doi: 10.1128/mcb.13.10.6180-6189.1993.
10
Changes in the stem-loop at the 3' terminus of histone mRNA affects its nucleocytoplasmic transport and cytoplasmic regulation.组蛋白mRNA 3'末端茎环结构的变化会影响其核质运输及细胞质调控。
Nucleic Acids Res. 1994 Nov 11;22(22):4660-6. doi: 10.1093/nar/22.22.4660.