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强直性脊柱炎患者外周血单核细胞中微小RNA成熟微处理器复合物组分(Drosha、Dicer和DGCR8)的表达水平。

Expression levels of the microRNA maturing microprocessor complex components; Drosha, Dicer, and DGCR8 in PBMCs from ankylosing spondylitis patients.

作者信息

Tabrizi Zeinab, Mansouri Reza, Aslani Saeed, Jamshidi Ahmad Reza, Mahmoudi Mahdi

机构信息

Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Immunology Department, Shahid Sadoughi University of Medical Sciences (International Campus), Yazd, Iran.

出版信息

Mediterr J Rheumatol. 2017 Jun 27;28(2):80-85. doi: 10.31138/mjr.28.2.80. eCollection 2017 Jun.

Abstract

OBJECTIVE/AIM: Two major enzymes in the microRNA maturation process, Dicer and Drosha, as well as DGCR8, the assistant of Drosha, function in the microprocessor complex. In this survey, the mRNA expression profiles of Drosha, Dicer, and DGCR8 in peripheral blood mononuclear cells (PBMCs) from ankylosing spondylitis (AS) patients and healthy controls were measured.

METHODS

Forty patients with AS and 40 age and gender matched healthy individuals were included in the study. PBMCs were separated, total RNA content of the cells was isolated, and first strand cDNA was synthesized. Quantitative analysis was performed through real-time PCR using the SYBR Green gene expression master mix.

RESULTS

AS cases expressed the Drosha mRNA almost equal to that of healthy controls (Fold Change= -0.94; P= 0.200). However, both Dicer and DGCR8 mRNA expressions were downregulated in patients relative to healthy subjects (Fold Change= -0.54 and -0.60; P= 0.002 and 0.004, respectively).

CONCLUSION

Our results suggest that downregulation of miRNA maturation components, namely Dicer and DGCR8 may be contributing in the pathogenesis procedure of AS.

摘要

目的

微小RNA成熟过程中的两种主要酶——Dicer和Drosha,以及Drosha的辅助因子DGCR8,在微处理器复合体中发挥作用。在本研究中,检测了强直性脊柱炎(AS)患者和健康对照者外周血单个核细胞(PBMC)中Drosha、Dicer和DGCR8的mRNA表达谱。

方法

本研究纳入40例AS患者和40例年龄及性别匹配的健康个体。分离PBMC,提取细胞总RNA含量,并合成第一链cDNA。使用SYBR Green基因表达预混液通过实时PCR进行定量分析。

结果

AS患者中Drosha mRNA的表达水平与健康对照者几乎相等(倍数变化=-0.94;P=0.200)。然而,与健康受试者相比,患者中Dicer和DGCR8的mRNA表达均下调(倍数变化分别为-0.54和-0.60;P分别为0.002和0.004)。

结论

我们的结果表明,微小RNA成熟成分Dicer和DGCR8的下调可能在AS的发病过程中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a547/7046025/4a8aec86f3b3/MJR-28-2-80-g001.jpg

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