Transcriptome Sequencing Analysis of Root in Soybean Responding to Mn Poisoning

نویسندگان

چکیده

Manganese (Mn) is among one of the essential trace elements for normal plant development; however, excessive Mn can cause growth and development to be hindered. Nevertheless, regulatory mechanisms root response poisoning remain unclear. In present study, results revealed that was inhibited when exposed poisoning. Physiological showed antioxidase enzyme activities (peroxidase, superoxide dismutase, ascorbate peroxidase, catalase) proline, malondialdehyde, soluble sugar contents increased significantly under toxicity stress (100 μM Mn), whereas protein four hormones’ (indolebutyric acid, abscisic indoleacetic gibberellic acid 3) decreased significantly. addition, Mn, Fe, Na, Al, Se in roots significantly, those Mg, Zn, K Furthermore, RNA sequencing (RNA-seq) analysis used test differentially expressed genes (DEGs) soybean The found 45,274 1430 DEGs concentrations 5 (normal) 100 (toxicity) μM. Among these DEGs, 572 were upregulated 858 downregulated, indicating may initiate complex molecular on stress. quantitative RT-PCR indicated many or downregulated markedly roots, suggesting regulation complex. Therefore, mechanism complicated. Present lay foundation further study function involved regulating tolerance traits roots.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Responding to pediatric poisoning.

Make sure you know how to act quickly if a child ingests a toxic substance and what to teach parents to prevent accidental poisonings.

متن کامل

Transcriptome analysis of the freshwater pearl mussel, Hyriopsis cumingii (Lea) Uusing Illumina paired-end sequencing to identify genes and markers

The transcriptome of triangle sail mussel Hyriopsis cumingii (Lea) using Illumina paired-end sequencing technology was conducted and analyzed. Equal quantities of total RNA isolated from six tissues, including gonads, hepatopancreas, foot, mantel, gills and adductor muscles, were pooled to construct a cDNA library. A total of 58.09 million clean reads with 98.48 % Q20 bases were generated. Clus...

متن کامل

Transcriptome analysis of the freshwater pearl mussel, Hyriopsis cumingii (Lea) Uusing Illumina paired-end sequencing to identify genes and markers

The transcriptome of triangle sail mussel Hyriopsis cumingii (Lea) using Illumina paired-end sequencing technology was conducted and analyzed. Equal quantities of total RNA isolated from six tissues, including gonads, hepatopancreas, foot, mantel, gills and adductor muscles, were pooled to construct a cDNA library. A total of 58.09 million clean reads with 98.48 % Q20 bases were generated. Clus...

متن کامل

Transcriptome analysis of the freshwater pearl mussel, Hyriopsis cumingii (Lea) using illumina paired-end sequencing to identify genes and markers

The transcriptome of triangle sail mussel Hyriopsis cumingii (Lea) using Illumina paired-end sequencing technology was conducted and analyzed. Equal quantities of total RNA isolated from six tissues, including gonad, hepatopancreas, foot, mantel, gill and adductor muscle, were pooled to construct a cDNA library. A total of 58.09 million clean reads with 98.48 % Q20 bases were generated. Cluster...

متن کامل

Transcriptome analysis of the freshwater pearl mussel, Hyriopsis cumingii (Lea) using illumina paired-end sequencing to identify genes and markers

The transcriptome of triangle sail mussel Hyriopsis cumingii (Lea) using Illumina paired-end sequencing technology was conducted and analyzed. Equal quantities of total RNA isolated from six tissues, including gonad, hepatopancreas, foot, mantel, gill and adductor muscle, were pooled to construct a cDNA library. A total of 58.09 million clean reads with 98.48 % Q20 bases were generated. Cluster...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: International Journal of Molecular Sciences

سال: 2023

ISSN: ['1661-6596', '1422-0067']

DOI: https://doi.org/10.3390/ijms241612727