miR396在豆科植物苜蓿根中對其菌根化和分生組織活性的影響ppt課件

1、2021-12-261miR396 affects mycorrhization and root meristem activity inthe legume Medicago truncatulaThe Plant Journal (2019)doi: 10.1111/tpj.121782021-12-262主要內(nèi)容nINTRODUCTIONnRESULTSn 1、 Mtr-miR396a and mtr-miR396b genes show different tissue-specific expression profiles in Medicago truncatula roots

2、n 2、In M. truncatula roots, miR396 regulates six GRF and two bHLH79 transcription factorsn 3、Characterization of the miR396 regulatory network in M. truncatulan 4、 miR396 negatively affects root growth, RAM size and cell proliferation in the root apexn 5、 Silencing of MtGRF genes mimics the miR396-O

3、E root growth phenotypen 6、 Hormonal control of miR396 expressionn 7、miR396 limits mycorrhizal colonization but not nodulation2021-12-263INTRODUCTIONnIn plants, root growth is controlled via coordinated cell division and expansion at the root apex, where three regions are observed: (i) the meristema

4、tic zone, (ii) the elongation zone, and (iii) the differentiation zonenRoot development is regulated by complex interactions of hormone signalling pathways2021-12-264nIn recent years, microRNAs (miRNAs) have emerged as important regulators of the architecture of the root systemnin Arabidopsis thalia

5、na, miR165/166 governs the radial patterning of vascular and pericycle tissues via quantitative repression of HD-ZIP III transcription factorsnA set of auxin-related miRNAs, including miR160, also regulate lateral root initiation and/or root growth2021-12-265nHowever, few miRNAs have been reported t

6、o play roles in RAM functionnAlthough large sets of mycorrhization or nodulation-responsive miRNAs have been identified in legumes, few have been functionally linked to these processes.2021-12-266nIn A. thaliana, miR396 is encoded by two loci, post-transcriptionally represses several members of the

7、growth-regulating factor (GRF) family. These plant-specific TFs control the growth and development of leaves and stems.nmiR396 may have evolved to play roles in various regulatory networks in plants.nIn this paper, we describe the roles of the miR396 regulatory network in M. truncatula roots.2021-12

8、-267RESULTSn1、Mtr-miR396a and mtr-miR396b genes show different tissue-specific expression profiles in Medicago truncatula rootsnMtr-miR396a 和 mtr-miR396b 在根中的表達(dá)具有空間特異性2021-12-2682021-12-269miR396 expression in organs and root tips兩種miRNAs在整株植物中都有表達(dá)，其中miR396b在根、瘤、葉和豆莢中的表達(dá)量較高，miR396a在根尖中較多2021-12-2610

9、兩者在根中的表達(dá)在根尖橫切面中的表達(dá)在根尖中的表達(dá)在側(cè)根中的表達(dá)2021-12-2611n2、In M. truncatula roots, miR396 regulates six GRF and two bHLH79 transcription factorsnWe found reads corresponding to the miR396-related cleavage products of six GRF mRNAs (MtGRF1, MtGi10-TC183867; MtGRF2, MtGi10-TC183494; MtGRF3, MtGi10 BG454006; MtGRF

10、4, Medtr5g027250; MtGRF5, Medtr8g020560; MtGRF6, Medtr7g126820). These transcripts possess a putative miR396 binding site, and the encoded proteins all contain the conserved domains of GRFsnWe also observed abundant degradome reads corresponding to specific cleavage of two non-GRF transcripts at miR

11、396 binding sites, Based on tBLASTX analysis, the 2 predicted proteins showed high similarity (43 and 46% respectively) to AtbHLH79/BIGPETAL (At1g59640), a TF involved in the control of petal growth in A. thaliana.2021-12-26122021-12-2613In M. truncatula, six MtGRF and two bHLH79 genes have miR396 b

12、inding sitesn3、Characterization of the miR396 regulatory network in M. truncatulanTo investigate miR396-mediated gene regulation in planta, we over-expressed mtr-miR396a and mtr-miR396b precursors in M. truncatula roots (miR396-OE).2021-12-2614左圖說明OE突變體能成功過量表達(dá)成熟的miRNAs2021-12-2615Levels of transcrip

13、ts of miR396 targets weremeasured using quantitative RT-PCR in miR396-OE rootsMtGRF-mRNA 水平和MtbHLH79轉(zhuǎn)錄水平都降低，說明miR396可能抑制這些基因的表達(dá)水平nTo further validate their targets, we generated roots expressing a target mimicry construct that was successfully designed to hinder miR396 activity in A. thaliana. Mimic

14、ry (MIM) transcripts specifically trap members of an miRNA family, and thus prevent their activity on endogenous targets2021-12-26162021-12-2617Levels of transcripts of miR396 targets weremeasured using quantitative RT-PCR in roots inactivated for miR396activity (MIM396)除了GRF6，其他基因表達(dá)水平都上升，這里還不能排除有其他

15、因子對GRF6進(jìn)行調(diào)節(jié)的可能，本文中沒有深入研究n4、miR396 negatively affects root growth, RAM size and cell proliferation in the root apexnTo investigate the function of miR396 in roots, we measured the length and dry weight of roots that either overexpressed the mtr-miR396b precursor (miR396-OE) or were inactivated for mi

16、R396 activity (MIM396).2021-12-26182021-12-2619miR396-OE 中主根長度和干重明顯減少，而MIM396中根長稍微增加，而干重卻大量增加。說明miR396過表達(dá)能抑制根的生長2021-12-2620Root meristem size is reduced inmiR396-OE composite plants2021-12-2621兩者之間沒有大的變化，說明miR396對細(xì)胞從細(xì)胞周期進(jìn)入分裂周期的開關(guān)沒有大的影響2021-12-2622The expression of mitotic cell cycle (CYCB1;1, CYCB1

17、;3, CYCB2;1, CYCD3;1, histone H4, CDC16) or endocycle (CCS52B) markers was measured using quantitativeRT-PCR in miR396-OE and control rootsThe percentage of cells replicating (i.e. EdU-positive nuclei) obtained from 20 root tips per constructin four independent experimentsnTogether, these data stron

18、gly suggest that miR396-dependent modulation of root growth may essentially be due to a restriction of cell division activity.2021-12-2623n5、Silencing of MtGRF genes mimics the miR396-OE root growth phenotypenTo study the role of the miR396 targets on root growth, we inactivated them using an RNAi s

19、trategy.nFirst, we generated composite plants expressing three RNAi constructs targeting a conserved region of various GRF genes ( MtGRF2, MtGRF4 and MtGRF6).nIn addition, we prepared an RNAi vector targeting both MtbHLH79 genes and confirmed their efficient silencing2021-12-26242021-12-2625Silencin

20、g of MtGRF genes mimics miR396 over-expression in roots.iGRF表達(dá)減少而ibHLH79表達(dá)不變，說明很可能是miR396對GRF基因的負(fù)調(diào)控使得miR396-OE和MIM396植株中根的生長表型不同n6、Hormonal control of miR396 expressionnWe treated wild-type plants for 1, 3 or 5 h with auxin, cytokinin, gibberellin, abscisic acid or brassinosteroids (BR), and measure

21、d pre-miR396 and target mRNA levels in roots.2021-12-26262021-12-2627Gibberellin, cytokinin and auxin treatments did not affectexpression of any of these genes2021-12-2628miR396b對ABA和BR 有明顯的反應(yīng)，并且GRF5在BR處理下下調(diào)，說明BR和miR396b, GRF5之間有某種作用關(guān)系2021-12-2629Levels of GUS transcript in roots expressing the prom

22、-miR396b:GUS construct (grey bars) or the prom-GRF5:GUS construct (black bars) treated or not treated with 1 nM BR for 3 h were measured using quantitative RT-PCR.BR可以活化miR396b的啟動子活性，但prom-GRF5:GUS并沒有明顯減少，說明BR可能是在轉(zhuǎn)錄后水平抑制GRF5基因的表達(dá)，而且BR和miR396b存在潛在聯(lián)系，但本文中沒有對其研究n7、 miR396 limits mycorrhizal colonizatio

23、n but not nodulationnWe next decided to study the potential role of miR396 in root symbioses.nWe analysed mtr-miR396a and mtr-miR396b expression profiles in roots inoculated with the symbiotic bacteria Sinorhizobium meliloti.2021-12-26302021-12-2631miR396a啟動子首先在根瘤導(dǎo)管組織中發(fā)現(xiàn)，miR396b啟動子在維管組織，感染區(qū)（）和氮固定區(qū)（）含量很高2021-12-2632雖然miR396存在于根瘤中，但miR396-OE和MIM396對根瘤密