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全基因组分析渗透胁迫下根系中应激响应基因和可变剪接变体。

Genome-Wide Analysis of Stress-Responsive Genes and Alternative Splice Variants in Roots under Osmotic Stresses.

机构信息

Korea Nanobiotechnology Center, Pusan National University, Busan 46241, Republic of Korea.

Department of Integrated Biological Science, Pusan National University, Busan 46241, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Sep 26;24(19):14580. doi: 10.3390/ijms241914580.

DOI:10.3390/ijms241914580
PMID:37834024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10573044/
Abstract

Plant roots show distinct gene-expression profiles from those of shoots under abiotic stress conditions. In this study, we performed mRNA sequencing (mRNA-Seq) to analyze the transcriptional profiling of roots under osmotic stress conditions-high salinity (NaCl) and drought (mannitol). The roots demonstrated significantly distinct gene-expression changes from those of the aerial parts under both the NaCl and the mannitol treatment. We identified 68 closely connected transcription-factor genes involved in osmotic stress-signal transduction in roots. Well-known abscisic acid (ABA)-dependent and/or ABA-independent osmotic stress-responsive genes were not considerably upregulated in the roots compared to those in the aerial parts, indicating that the osmotic stress response in the roots may be regulated by other uncharacterized stress pathways. Moreover, we identified 26 osmotic-stress-responsive genes with distinct expressions of alternative splice variants in the roots. The quantitative reverse-transcription polymerase chain reaction further confirmed that alternative splice variants, such as those for , , , and , were differentially expressed in the roots, suggesting that alternative splicing is an important regulatory mechanism in the osmotic stress response in roots. Altogether, our results suggest that tightly connected transcription-factor families, as well as alternative splicing and the resulting splice variants, are involved in the osmotic stress response in roots.

摘要

在非生物胁迫条件下,植物根系的基因表达谱与地上部分明显不同。在这项研究中,我们进行了 mRNA 测序(mRNA-Seq),以分析渗透胁迫条件下(高盐度(NaCl)和干旱(甘露醇))根系的转录谱。与 NaCl 和甘露醇处理的地上部分相比,根系表现出明显不同的基因表达变化。我们鉴定了 68 个与根系渗透胁迫信号转导密切相关的转录因子基因。与地上部分相比,众所周知的依赖脱落酸(ABA)和/或独立于 ABA 的渗透胁迫响应基因在根系中没有被显著上调,这表明根系的渗透胁迫反应可能由其他未被描述的胁迫途径调节。此外,我们还鉴定了 26 个在根系中具有不同表达的替代剪接变体的渗透胁迫响应基因。定量反转录聚合酶链反应进一步证实,替代剪接变体,如 、 、 、 和 ,在根系中差异表达,表明替代剪接是根系渗透胁迫反应的一个重要调节机制。总之,我们的结果表明,紧密连接的转录因子家族以及替代剪接和由此产生的剪接变体,参与了根系的渗透胁迫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/8e7abdaf79a4/ijms-24-14580-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/fcfc3f8fac17/ijms-24-14580-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/306a6e5a7f29/ijms-24-14580-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/2e5aab6cb6ec/ijms-24-14580-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/d3d44f920150/ijms-24-14580-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/3c58302cc469/ijms-24-14580-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/7e9dd3b634e1/ijms-24-14580-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/777579b9b479/ijms-24-14580-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/8e7abdaf79a4/ijms-24-14580-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/fcfc3f8fac17/ijms-24-14580-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/306a6e5a7f29/ijms-24-14580-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/2e5aab6cb6ec/ijms-24-14580-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/d3d44f920150/ijms-24-14580-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/3c58302cc469/ijms-24-14580-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/7e9dd3b634e1/ijms-24-14580-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/777579b9b479/ijms-24-14580-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8206/10573044/8e7abdaf79a4/ijms-24-14580-g008.jpg

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