scholarly journals Tissue-specific transposon-associated small RNAs in the gymnosperm tree, Norway spruce

BMC Genomics ◽  
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Miyuki Nakamura ◽  
Claudia Köhler ◽  
Lars Hennig
Keyword(s):  
Norway Spruce ◽  
Small Rnas ◽  
Male Gametophyte ◽  
Leaf Tissue ◽  
Tissue Specific ◽  
Size Classes ◽  
Vegetative Tissues ◽  
Male Cones ◽  
Transposon Activity ◽  
Angiosperm Pollen

Abstract Background Small RNAs (sRNAs) are regulatory molecules impacting on gene expression and transposon activity. MicroRNAs (miRNAs) are responsible for tissue-specific and environmentally-induced gene repression. Short interfering RNAs (siRNA) are constitutively involved in transposon silencing across different type of tissues. The male gametophyte in angiosperms has a unique set of sRNAs compared to vegetative tissues, including phased siRNAs from intergenic or genic regions, or epigenetically activated siRNAs. This is contrasted by a lack of knowledge about the sRNA profile of the male gametophyte of gymnosperms. Results Here, we isolated mature pollen from male cones of Norway spruce and investigated its sRNA profiles. While 21-nt sRNAs is the major size class of sRNAs in needles, in pollen 21-nt and 24-nt sRNAs are the most abundant size classes. Although the 24-nt sRNAs were exclusively derived from TEs in pollen, both 21-nt and 24-nt sRNAs were associated with TEs. We also investigated sRNAs from somatic embryonic callus, which has been reported to contain 24-nt sRNAs. Our data show that the 24-nt sRNA profiles are tissue-specific and differ between pollen and cell culture. Conclusion Our data reveal that gymnosperm pollen, like angiosperm pollen, has a unique sRNA profile, differing from vegetative leaf tissue. Thus, our results reveal that angiosperm and gymnosperm pollen produce new size classes not present in vegetative tissues; while in angiosperm pollen 21-nt sRNAs are generated, in the gymnosperm Norway spruce 24-nt sRNAs are generated. The tissue-specific production of distinct TE-derived sRNAs in angiosperms and gymnosperms provides insights into the diversification process of sRNAs in TE silencing pathways between the two groups of seed plants.

scholarly journals Tissue-Specific Knockdown of Genes of the Argonaute Family Modulates Lifespan and Radioresistance in Drosophila Melanogaster

2021 ◽  
Author(s):  
Ekaterina N. Proshkina ◽  
Elena Yushkova ◽  
Liubov Koval ◽  
Nadezhda Zemskaya ◽  
Evgeniya Shchegoleva ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Small Rnas ◽  
Molecular Mechanisms ◽  
Fat Body ◽  
Expression Patterns ◽  
Regulation Of Gene Expression ◽  
Stress Factors ◽  
Tissue Specific ◽  
Argonaute Family ◽  
Transposon Activity

Small RNAs are essential for the coordination of many cellular processes, including the regulation of gene expression patterns, the prevention of genomic instability, and the suppression of mutagenic transposon activity. These processes determine aging, longevity, and sensitivity of cells and an organism to stress factors (particularly, ionizing radiation). The biogenesis and activity of small RNAs are provided by proteins of the Argonaute family. These proteins participate in the processing of small RNA precursors and the formation of an RNA-induced silencing complex. However, the role of Argonaute proteins in the regulation of lifespan and radioresistance remains poorly explored. We studied the effect of knockdown of Argonaute genes (AGO1, AGO2, AGO3, piwi) in various tissues on the Drosophila melanogaster lifespan and survival after the γ-irradiation at a dose of 700 Gy. In most cases, these parameters were reduced or did not change significantly in flies with tissue-specific RNA interference. Surprisingly, piwi knockdown in both the fat body and the nervous system caused a lifespan increase. But changes in radioresistance depended on the tissue in which the gene was knocked out. In addition, analysis of changes in retrotransposon levels and expression of stress response genes allowed us to determine associated molecular mechanisms.

scholarly journals Successive accumulation of two size classes of viroid-specific small RNA in potato spindle tuber viroid-infected tomato plants

2007 ◽  
Vol 88 (12) ◽  
pp. 3452-3457 ◽  
Author(s):  
Satoru Machida ◽  
Naoki Yamahata ◽  
Hiromi Watanuki ◽  
Robert A. Owens ◽  
Teruo Sano
Keyword(s):  
Small Rna ◽  
Small Rnas ◽  
Rna Silencing ◽  
Time Course ◽  
Leaf Tissue ◽  
Potato Spindle Tuber Viroid ◽  
Size Classes ◽  
Infected Tomato ◽  
Symptomatic Leaf ◽  
Rna Accumulation

Like many plant RNA viruses, infection by potato spindle tuber viroid (PSTVd) is known to lead to RNA silencing and a marked reduction in visible disease. To examine the relationship between RNA silencing and this recovery phenomenon in greater detail, we have carried out time-course analyses of viroid-specific small RNA accumulation using several viroid–host combinations. These analyses revealed the presence of two size classes of viroid-specific small RNAs in infected plants, and sequence analysis subsequently demonstrated the presence of a previously undescribed cluster of small RNAs derived primarily from negative-strand PSTVd RNA. Although the clustering patterns were similar, the size distribution of PSTVd small RNAs isolated from symptomatic leaf tissue became more heterogeneous with time. The process by which viroid-specific small RNAs are generated appears to be more complicated than previously believed, possibly involving multiple DICER-LIKE activities, viroid RNA substrates and subcellular compartments.

Dissecting the genetic control of root and leaf tissue-specific anthocyanin pigmentation in carrot (Daucus carota L.)

2019 ◽  
Vol 132 (9) ◽  
pp. 2485-2507 ◽  
Author(s):  
Florencia Bannoud ◽  
Shelby Ellison ◽  
Marcos Paolinelli ◽  
Thomas Horejsi ◽  
Douglas Senalik ◽  
...  
Keyword(s):  
Genetic Control ◽  
Daucus Carota ◽  
Leaf Tissue ◽  
Anthocyanin Pigmentation ◽  
Tissue Specific ◽  
Daucus Carota L

scholarly journals Oxidative Medicine and Cellular Longevity Changes in the Small RNA Expression in Endothelial Cells in Response to Inflammatory Stimulation

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Peixi Liu ◽  
Liuxun Hu ◽  
Yuan Shi ◽  
Yingjun Liu ◽  
Guo Yu ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Small Rna ◽  
Small Rnas ◽  
Cerebrovascular Diseases ◽  
Differentially Expressed ◽  
Small Rna Sequencing ◽  
Rna Expression ◽  
Tissue Specific ◽  
Qrt Pcr ◽  
Tnf Α

Objective. Endothelial cell inflammation is a common pathophysiological process in many cardiovascular and cerebrovascular diseases. Small RNA is a kind of short nonprotein coding RNA molecule. Changes in the small RNA expression in endothelial cells have been linked to the development of cardiovascular and cerebrovascular diseases. We investigated and verified differentially expressed small RNAs in endothelial cells in response to inflammatory stimulation. Methods. Primary rat endothelial cells were obtained from Sprague-Dawley rats and treated with 10 ng/ml TNF-α for 24 hours. Small RNA sequencing was used to generate extensive small RNA data. Significantly differentially expressed small RNAs identified in the analysis were further confirmed by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Then, we investigated the tissue-specific small RNA expression after RNA extraction from different tissues. Results. Small RNA sequencing demonstrated that 17 miRNAs, 1 piRNA, 10 snoRNAs, and 7 snRNAs were significantly differentially expressed. qRT-PCR identified 3 miRNAs, 2 snoRNAs, and 2 snRNAs with significantly different expression. Analysis of the tissue-specific expression showed that rno-miR-126a-5p was predominantly expressed in the lung, rno-miR-146a-5p in the intestines, and rno-novel-178 in the heart. Rno-piR-017330 was mainly expressed in the muscle. snoR-8966.1 was predominantly expressed in the bone. snoR-6253.1 was mostly expressed in the vessels and bone. snR-29469.1 was mainly expressed in the bone, and snR-85806.1 was predominantly expressed in the vessels and bone. Conclusions. We report for the first time the expression of small RNAs in endothelial cells under inflammatory conditions. TNF-α can regulate the expression of small RNAs in endothelial cells, and their expression is tissue-specific.

scholarly journals Dynamic regulation of chromatin topology and transcription by inverted repeat-derived small RNAs in sunflower

2019 ◽  
Vol 116 (35) ◽  
pp. 17578-17583 ◽  
Author(s):  
Delfina Gagliardi ◽  
Damian A. Cambiagno ◽  
Agustin L. Arce ◽  
Ariel H. Tomassi ◽  
Jorge I. Giacomelli ◽  
...  
Keyword(s):  
Chromatin Remodeling ◽  
Inverted Repeat ◽  
Small Rnas ◽  
Rna Silencing ◽  
De Novo ◽  
Epigenetic Modification ◽  
Regulatory Elements ◽  
Dynamic Regulation ◽  
Transposon Activity ◽  
De Novo Methylation

Transposable elements (TEs) are extremely abundant in complex plant genomes. siRNAs of 24 nucleotides in length control transposon activity in a process that involves de novo methylation of targeted loci. Usually, these epigenetic modifications trigger nucleosome condensation and a permanent silencing of the affected loci. Here, we show that a TE-derived inverted repeat (IR) element, inserted near the sunflower HaWRKY6 locus, dynamically regulates the expression of the gene by altering chromatin topology. The transcripts of this IR element are processed into 24-nt siRNAs, triggering DNA methylation on its locus. These epigenetic marks stabilize the formation of tissue-specific loops in the chromatin. In leaves, an intragenic loop is formed, blocking HaWRKY6 transcription. While in cotyledons (Cots), formation of an alternative loop, encompassing the whole HaWRKY6 gene, enhances transcription of the gene. The formation of this loop changes the promoter directionality, reducing IR transcription, and ultimately releasing the loop. Our results provide evidence that TEs can act as active and dynamic regulatory elements within coding loci in a mechanism that combines RNA silencing, epigenetic modification, and chromatin remodeling machineries.

scholarly journals Genome-wide sequencing of small RNAs reveals a tissue-specific loss of conserved microRNA families in Echinococcus granulosus

BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 736 ◽  
Author(s):  
Yun Bai ◽  
Zhuangzhi Zhang ◽  
Lei Jin ◽  
Hui Kang ◽  
Yongqiang Zhu ◽  
...  
Keyword(s):  
Echinococcus Granulosus ◽  
Small Rnas ◽  
Tissue Specific ◽  
Specific Loss ◽  
Genome Wide

scholarly journals Tissue-specific mRNA profiling of the Brassica napus-Sclerotinia sclerotiorum interaction uncovers novel regulators of plant immunity

2021 ◽  
Author(s):  
Philip Walker ◽  
Ian Girard ◽  
Shayna Giesbrecht ◽  
Steve Whyard ◽  
Dilantha Fernando ◽  
...  
Keyword(s):  
Brassica Napus ◽  
Sclerotinia Sclerotiorum ◽  
Defense Response ◽  
Plant Immunity ◽  
Leaf Tissue ◽  
Specific Gene ◽  
Tissue Specific ◽  
Biotrophic Pathogens ◽  
Dna Insertion ◽  
Insight Into

White mold in Brassica napus (canola) is caused by the fungal pathogen Sclerotinia sclerotiorum and is responsible for significant losses in crop yield across the globe. With advances in high-throughput transcriptomics, our understanding of the B. napus defense response to S. sclerotiorum is becoming clearer; however, the response of individual tissue layers directly at the site of infection has yet to be explored. Using laser microdissection coupled with RNA sequencing, we profiled the epidermis, mesophyll and vascular leaf tissue layers in response to S. sclerotiorum. This strategy increases the number of genes detected compared to whole-leaf assessments and provides unprecedented information on tissue-specific gene expression networks in response to pathogen attack. Our findings provide novel insight into the conserved and specific roles of ontogenetically distinct leaf tissue layers in response to infection. Using bioinformatics tools, we identified several defense genes that might coordinate plant immunity responses shared across different tissue layers within the leaf. These genes were functionally characterized by challenging T-DNA insertion lines of Arabidopsis with necrotrophic, hemi-biotrophic, and biotrophic pathogens, ultimately converging on the PR5-like RECEPTOR KINASE (PRK5). Together, these data provide insight on the complexity of the B. napus defense response directly at the site of infection.

scholarly journals Do Small RNAs Interfere With LINE-1?

2006 ◽  
Vol 2006 ◽  
pp. 1-8 ◽  
Author(s):  
Harris S. Soifer
Keyword(s):  
Transposable Elements ◽  
Human Genome ◽  
Small Rnas ◽  
Substantial Evidence ◽  
Rnai Machinery ◽  
Rna Sequences ◽  
Direct Role ◽  
Long Interspersed Elements ◽  
Extensive Analysis ◽  
Transposon Activity

Long interspersed elements (LINE-1 or L1) are the most active transposable elements in the human genome. Due to their high copy number and ability to sponsor retrotransposition of nonautonomous RNA sequences, unchecked L1 activity can negatively impact the genome by a number of means. Substantial evidence in lower eukaryotes demonstrates that the RNA interference (RNAi) machinery plays a major role in containing transposon activity. Despite extensive analysis in other eukaryotes, no experimental evidence has been presented that L1-derived siRNAs exist, or that the RNAi plays a significant role in restricting L1 activity in the human genome. This review will present evidence showing a direct role for RNAi in suppressing the movement of transposable elements in other eukaryotes, as well as speculate on the role RNAi might play in protecting the human genome from LINE-1 activity.

scholarly journals Tissue-Specific Knockdown of Genes of the Argonaute Family Modulates Lifespan and Radioresistance in Drosophila melanogaster

2021 ◽  
Vol 22 (5) ◽  
pp. 2396
Author(s):  
Ekaterina Proshkina ◽  
Elena Yushkova ◽  
Liubov Koval ◽  
Nadezhda Zemskaya ◽  
Evgeniya Shchegoleva ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Small Rnas ◽  
Molecular Mechanisms ◽  
Fat Body ◽  
Expression Patterns ◽  
Regulation Of Gene Expression ◽  
Stress Factors ◽  
Γ Irradiation ◽  
Tissue Specific ◽  
Argonaute Family

Small RNAs are essential to coordinate many cellular processes, including the regulation of gene expression patterns, the prevention of genomic instability, and the suppression of the mutagenic transposon activity. These processes determine the aging, longevity, and sensitivity of cells and an organism to stress factors (particularly, ionizing radiation). The biogenesis and activity of small RNAs are provided by proteins of the Argonaute family. These proteins participate in the processing of small RNA precursors and the formation of an RNA-induced silencing complex. However, the role of Argonaute proteins in regulating lifespan and radioresistance remains poorly explored. We studied the effect of knockdown of Argonaute genes (AGO1, AGO2, AGO3, piwi) in various tissues on the Drosophila melanogaster lifespan and survival after the γ-irradiation at a dose of 700 Gy. In most cases, these parameters are reduced or did not change significantly in flies with tissue-specific RNA interference. Surprisingly, piwi knockdown in both the fat body and the nervous system causes a lifespan increase. But changes in radioresistance depend on the tissue in which the gene was knocked out. In addition, analysis of changes in retrotransposon levels and expression of stress response genes allow us to determine associated molecular mechanisms.

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