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哮喘候选基因在人及鼠肺发育过程中的表达分析。

Expression analysis of asthma candidate genes during human and murine lung development.

机构信息

Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Respir Res. 2011 Jun 23;12(1):86. doi: 10.1186/1465-9921-12-86.

Abstract

BACKGROUND

Little is known about the role of most asthma susceptibility genes during human lung development. Genetic determinants for normal lung development are not only important early in life, but also for later lung function.

OBJECTIVE

To investigate the role of expression patterns of well-defined asthma susceptibility genes during human and murine lung development. We hypothesized that genes influencing normal airways development would be over-represented by genes associated with asthma.

METHODS

Asthma genes were first identified via comprehensive search of the current literature. Next, we analyzed their expression patterns in the developing human lung during the pseudoglandular (gestational age, 7-16 weeks) and canalicular (17-26 weeks) stages of development, and in the complete developing lung time series of 3 mouse strains: A/J, SW, C57BL6.

RESULTS

In total, 96 genes with association to asthma in at least two human populations were identified in the literature. Overall, there was no significant over-representation of the asthma genes among genes differentially expressed during lung development, although trends were seen in the human (Odds ratio, OR 1.22, confidence interval, CI 0.90-1.62) and C57BL6 mouse (OR 1.41, CI 0.92-2.11) data. However, differential expression of some asthma genes was consistent in both developing human and murine lung, e.g. NOD1, EDN1, CCL5, RORA and HLA-G. Among the asthma genes identified in genome wide association studies, ROBO1, RORA, HLA-DQB1, IL2RB and PDE10A were differentially expressed during human lung development.

CONCLUSIONS

Our data provide insight about the role of asthma susceptibility genes during lung development and suggest common mechanisms underlying lung morphogenesis and pathogenesis of respiratory diseases.

摘要

背景

人们对大多数哮喘易感基因在人类肺部发育过程中的作用知之甚少。正常肺发育的遗传决定因素不仅在生命早期很重要,而且对以后的肺功能也很重要。

目的

研究明确的哮喘易感基因在人类和鼠类肺部发育过程中的表达模式。我们假设,影响正常气道发育的基因在与哮喘相关的基因中会被过度表达。

方法

首先通过全面搜索当前文献,确定哮喘基因。接下来,我们分析了这些基因在人类肺部发育的假腺期(妊娠龄 7-16 周)和小管期(17-26 周)以及 3 个鼠种的完整发育肺时间序列中的表达模式:A/J、SW、C57BL6。

结果

总共在文献中确定了 96 个与至少两种人类人群中的哮喘相关的基因。总体而言,在肺发育过程中差异表达的基因中,没有发现哮喘基因的显著过度表达,尽管在人类(比值比,OR 1.22,置信区间,CI 0.90-1.62)和 C57BL6 鼠(OR 1.41,CI 0.92-2.11)数据中存在趋势。然而,一些哮喘基因在发育中的人类和鼠类肺中的表达差异是一致的,例如 NOD1、EDN1、CCL5、RORA 和 HLA-G。在全基因组关联研究中确定的哮喘基因中,ROBO1、RORA、HLA-DQB1、IL2RB 和 PDE10A 在人类肺发育过程中差异表达。

结论

我们的数据提供了哮喘易感基因在肺发育过程中的作用的见解,并表明了肺部形态发生和呼吸疾病发病机制的共同机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6416/3141421/faa42aaa86fb/1465-9921-12-86-1.jpg

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