|
|
Fine Mapping and Candidate Gene Analysis of Maize (Zea mays) Sex Determination Gene tasselseed10 |
ZHU Si-Ying*, ZHU Ting-Ting*, LI Ting, DENG Ping, XIANG Xiao-Qin, WANG Jiu-Guang, WANG Guo-Qiang, LIU Chao-Xian** |
Maize Research Institute/ Engineering Research Center of South Upland Agriculture, Ministry of Education/ Chongqing Key Laboratory of Crop Molecular Improvement, Southwest University, Beibei 400715; China |
|
|
Abstract Maize (Zea mays) is an important model plant to decipher the molecular mechanism of sex determination. The research on sex determination of tassel and ear is of great significance to improve the inflorescence architecture and increase yield. In this study, a maize sex determination mutant tasselseed10 (ts10) that could produce kernel on tassel was identified by treating B73 pollen with ethyl methane sulfonate (EMS). In fields, the vegetative growth of the ts10 was normal. When tassels emerged, the spikelets on middle and upper of main spikes and branches showed sex reversal, which could produce a large quantity of silks. While the apical spikelets could shed pollens normally. Phenotype observation under scanning electron microscope indicated when the male inflorescence meristem of ts10 was about 12 mm long, the florets produced feminized structure. Using map-based cloning strategy, the ts10 gene was narrowed down to a region of about 600 kb between the SSR markers PL4 and PR5 on Chr.1, which harbored 7 annotated genes. Sequencing analysis revealed that only the myelocytomatosis 7 (ZmMyc7) produced a mutation in which the 1 594th base G was substituted by base a resulting in the 532nd amino acid glutamic acid substituted by lysine. Further analysis suggested the mutation was located at the conserved domain HLH of ZmMyc7. Expression analysis showed that ts10 was expressed in root, stem, leaf, immature tassel, immature ear and kernel, among which the expression level in ear was the highest, followed by tassel; in addition, except for leaf, there was no significant difference in expression level of ZmMyc7 between ts10 and normal plants in root, stem, immature tassel, immature ear, embryo and endosperm. The subcellular localization results showed ZmMyc7 functions in nucleus. This study provides further theoretical support and genetic resources for enriching the molecular mechanism of sex determination in maize.
|
Received: 12 June 2024
|
|
Corresponding Authors:
** cauxian@163.com
|
About author:: * These authors contributed equally to this work |
|
|
|
[1] 秦利萍, 董二飞, 白洋, 等. 2020. 玉米tasselseed突变体ts12的遗传分析与分子鉴定[J]. 作物学报, 46(05): 690-699. (Qin L P, Dong E F, Bai Y, et al.2020. Genetic analysis and molecular characterization of tasselseed mutant ts12 in maize[J]. Acta Agronomica Sinica, 46(05): 690-699.) [2] Acosta I F, Laparra H, Romero S P, et al.2009. tasselseed1 is a lipoxygenase affecting jasmonic acid signaling in sex determination of maize[J]. Science, 323(5911): 262-265. [3] Agrawal G K, Abe K, Yamazaki M, et al.2005. Conservation of the E-function for floral organ identity in rice revealed by the analysis of tissue culture-induced loss-of-function mutants of the OsMADS1 gene[J]. Plant Molecular Biology, 59(1): 125-135. [4] Bensen R J, Johal G S, Crane V C, et al.1995. Cloning and characterization of the maize An1 gene[J]. Plant Cell, 7(1): 75-84. [5] Cai Q, Yuan Z, Chen M J, et al.2014. Jasmonic acid regulates spikelet development in rice[J]. Nature Communications, 5: 3476. [6] Calderon-Urrea A, Dellaporta S L.1999. Cell death and cell protection genes determine the fate of pistils in maize[J]. Development, 126(3): 435-441. [7] Chen Y, Hou M M, Liu L J, et al.2014. The maize DWARF1 encodes a gibberellin 3-oxidase and is dual localized to the nucleus and cytosol[J]. Plant Physiology, 166(4): 2028-2039. [8] Chen S K, Zhao H Y, Luo T L, et al.2019. Characteristics and expression pattern of MYC genes in Triticum aestivum, Oryza sativa, and Brachypodium distachyon[J]. Plants (Basel), 8(8): 274. [9] Chuck G, Meeley R, Irish E, et al.2007. The maize tasselseed4 microRNA controls sex determination and meristem cell fate by targeting Tasselseed6/indeterminate spikelet1[J]. Nature Genetics, 39(12): 1517-1521. [10] Chuck G, Meeley R B, Hake S.1998. The control of maize spikelet meristem fate by the APETALA2-like gene indeterminate spikelet1[J]. Genes and Development, 12(8): 1145-1154. [11] Engelberth J, Contreras C F, Viswanathan S.2012. Transcriptional analysis of distant signaling induced by insect elicitors and mechanical wounding in Zea mays[J]. PLOS ONE, 7(4): e34855. [12] Fernández-Calvo P, Chini A, Fernández-Barbero G, et al.2011. The Arabidopsis bHLH transcription factors MYC3 and MYC4 are targets of JAZ repressors and act additively with MYC2 in the activation of jasmonate responses[J]. Plant Cell, 23(2):701-715. [13] Fu J Y, Ren F, Lu X, et al.2016. A tandem array of ent-kaurene synthases in maize with roles in gibberellin and more specialized metabolism[J]. Plant Physiology, 170(2): 742-751. [14] Hartwig T, Chuck G S, Fujioka S, et al.2011. Brassinosteroid control of sex determination in maize[J]. Proceedings of the National Academy of Sciences of the USA, 108(49): 19814-19819. [15] Hayward A P, Moreno M A, Howard T P, et al.2016. Control of sexuality by the sk1-encoded UDP-glycosyltransferase of maize[J]. Science Advances, 2(10): e1600991. [16] Kazan K, Manners J M.2008. Jasmonate signaling: toward an integrated view[J]. Plant Physiology, 146(4): 1459-1468. [17] Kazan K, Manners J M.2013. MYC2: The master in action[J]. Molecular Plant, 6(3): 686-703. [18] Lawit S J, Wych H M, Xu D P, et al.2010. Maize DELLA proteins dwarf plant8 and dwarf plant9 as modulators of plant development[J]. Plant and Cell Physiology, 51(11): 1854-1868. [19] Luo H S, Meng D X, Liu H B, et al.2020. Ectopic Expression of the transcriptional regulator silky3 causes pleiotropic meristem and sex determination defects in maize inflorescences[J]. Plant Cell, 32(12): 3750-3773. [20] Noguchi T, Fujioka S, Takatsuto S, et al.1999. Arabidopsis det2 is defective in the conversion of (24R)-24-methylcholest-4-En-3-one to (24R)-24-methyl-5alpha-cholestan-3-one in brassinosteroid biosynthesis[J]. Plant Physiology, 120(3): 833-840. [21] Parkinson S E, Gross S M, Hollick J B.2007. Maize sex determination and abaxial leaf fates are canalized by a factor that maintains repressed epigenetic states[J]. Developmental Biology, 308(2): 462-473. [22] Paterson A H, Bowers J E, Chapman B A.2004. Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics[J]. Proceedings of the National Academy of Sciences of the USA, 101(26): 9903-9908. [23] Pires N, Dolan L.2010. Origin and diversification of basic-helix-loop-helix proteins in plants[J]. Molecular Biology and Evolution, 27(4): 862-874. [24] Prasad K, Parameswaran S, Vijayraghavan U.2005. OsMADS1, a rice MADS-box factor, controls differentiation of specific cell types in the lemma and palea and is an early-acting regulator of inner floral organs[J]. The Plant Journal, 43(6): 915-928. [25] Silverstone A L, Jung H S, Dill A, et al.2001. Repressing a repressor: Gibberellin-induced rapid reduction of the RGA protein in Arabidopsis[J]. Plant Cell, 13(7): 1555-1566. [26] Thiel T, Kota R, Grosse I, et al.2004. SNP2CAPS: A SNP and INDEL analysis tool for CAPS marker development[J]. Nucleic Acids Research, 32(1): e5. [27] Wang F, Yuan Z J, Zhao Z W, et al.2020. Tasselseed5 encodes a cytochrome C oxidase that functions in sex determination by affecting jasmonate catabolism in maize[J]. Journal of Integrative Plant Biology, 62(2): 247-255. [28] Winkler R G, Helentjaris T.1995. The maize Dwarf3 gene encodes a cytochrome P450-mediated early step in gibberellin biosynthesis[J]. Plant Cell, 7(8): 1307-1317. [29] Yang Y F, Zhang K K, Yang L Y, et al.2018. Identification and characterization of MYC transcription factors in Taxus sp.[J]. Gene, 675: 1-8. |
|
|
|