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小RNA的深度测序有助于斑马鱼中与组织和性别相关的微小RNA的发现。

Deep sequencing of small RNA facilitates tissue and sex associated microRNA discovery in zebrafish.

作者信息

Vaz Candida, Wee Choon Wei, Lee Gek Ping Serene, Ingham Philip W, Tanavde Vivek, Mathavan Sinnakaruppan

机构信息

Bioinformatics Institute, Agency for Science Technology and Research, 30 Biopolis Street, #07-01 Matrix, Singapore, 138671, Singapore.

Molecular Genomics (P) Ltd, 51 Science Park Road, #04-16 The ARIES, Singapore, 117586, Singapore.

出版信息

BMC Genomics. 2015 Nov 16;16:950. doi: 10.1186/s12864-015-2135-7.

Abstract

BACKGROUND

The role of microRNAs in gene regulation has been well established. The extent of miRNA regulation also increases with increasing genome complexity. Though the number of genes appear to be equal between human and zebrafish, substantially less microRNAs have been discovered in zebrafish compared to human (miRBase Release 19). It appears that most of the miRNAs in zebrafish are yet to be discovered.

RESULTS

We sequenced small RNAs from brain, gut, liver, ovary, testis, eye, heart and embryo of zebrafish. In brain, gut and liver sequencing was done sex specifically. Majority of the sequenced reads (16-62 %) mapped to known miRNAs, with the exception of ovary (5.7 %) and testis (7.8 %). Using the miRNA discovery tool (miRDeep2), we discovered novel miRNAs from the unannotated reads that ranged from 7.6 to 23.0 %, with exceptions of ovary (51.4 %) and testis (55.2 %). The prediction tool identified a total of 459 novel pre-miRNAs. We compared expression of miRNAs between different tissues and between males and females to identify tissue associated and sex associated miRNAs respectively. These miRNAs could serve as putative biomarkers for these tissues. The brain and liver had highest number of tissue associated (22) and sex associated (34) miRNAs, respectively.

CONCLUSIONS

This study comprehensively identifies tissue and sex associated miRNAs in zebrafish. Further, we have discovered 459 novel pre-miRNAs (~30 % seed homology to human miRNA) as a genomic resource which can facilitate further investigations to understand miRNA-mRNA gene regulatory networks in zebrafish which will have implications in understanding the function of human homologs.

摘要

背景

微小RNA在基因调控中的作用已得到充分证实。随着基因组复杂性的增加,微小RNA调控的程度也会提高。尽管人类和斑马鱼的基因数量看似相等,但与人类相比,在斑马鱼中发现的微小RNA数量要少得多(miRBase第19版)。斑马鱼中的大多数微小RNA似乎尚未被发现。

结果

我们对斑马鱼的脑、肠、肝、卵巢、睾丸、眼睛、心脏和胚胎中的小RNA进行了测序。在脑、肠和肝中,测序是按性别特异性进行的。除卵巢(5.7%)和睾丸(7.8%)外,大多数测序读数(16 - 62%)映射到已知的微小RNA。使用微小RNA发现工具(miRDeep2),我们从未注释的读数中发现了新的微小RNA,其比例在7.6%至23.0%之间,卵巢(51.4%)和睾丸(55.2%)除外。该预测工具总共鉴定出459个新的前体微小RNA。我们比较了不同组织之间以及雄性和雌性之间微小RNA的表达,分别确定与组织相关和与性别相关的微小RNA。这些微小RNA可作为这些组织的假定生物标志物。脑和肝分别具有最多数量的与组织相关(22个)和与性别相关(34个)的微小RNA。

结论

本研究全面鉴定了斑马鱼中与组织和性别相关的微小RNA。此外,我们发现了459个新的前体微小RNA(与人类微小RNA的种子同源性约为30%)作为基因组资源,这有助于进一步研究以了解斑马鱼中的微小RNA - mRNA基因调控网络,这将对理解人类同源物的功能具有重要意义。

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