Gene MS33 related to maize male nuclear sterility and application thereof in cross breeding
A technology of male sterility and male fertility, applied in application, genetic engineering, plant genetic improvement, etc., can solve problems such as limited nuclear sterility genes, and achieve the effect of complete traits
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Embodiment 1
[0060] Example 1. Map-based cloning of the gene MS33 related to maize male sterility
[0061] 1. Phenotype identification of maize ms33 mutant
[0062] The maize male sterile 33 (ms33) mutant was discovered in 1999, and there are 8 alleles of the ms33 mutant preserved in the U.S. Maize Genetics Cooperation Stock Center public mutant bank at present, and the inventor of the present invention applied for The ms33 mutant allele ms33-6019 (ie maize mutant ms33-6019) was obtained and phenotyped. turn out. Compared with wild-type maize plants (inbred line Zheng 58), the ms33-6019 mutant showed no significant difference in pollen abortion and vegetative growth stage ( figure 1 Middle A), but when the ms33-6019 mutant plant entered the pollination stage, the anthers could not be spit out from the florets. Through microdissection and fertility identification, it was found that the ms33-6019 mutant anthers were severely atrophied, and the anthers were treated with 1% I 2 -KI soluti...
Embodiment 2
[0075] Example 2, Maize ms33 Mutant MS33 Gene Functional Complementation Experiment
[0076] In order to further prove and confirm that the ms33 mutant phenotype is caused by the mutation of the MS33 gene, the inventors of the present invention conducted another ms33 allelic mutant line ms33-6024 (that is, the maize mutant ms33-6024, which has the same male sterility as ms33-6019) traits) genome sequencing, and found that compared with the wild-type maize plant—inbred line Zheng 58, the sequence difference of the ms33-6024 mutant was only the insertion of 2 bases at the 507 bp base in the coding region of the MS33 gene, which resulted in migration code mutation, premature termination of translation ( image 3 Middle B).
[0077] At the same time, the inventors of the present invention screened a new ms33 mutant allele sa1 in the self-developed MuDR mutant library. The heterozygous fertile plants (+ / ms33) from the ms33-6019 allele were pollinated to the sa1 homozygous sterile...
Embodiment 3
[0079] Embodiment 3, the expression analysis of MS33 gene in each organ
[0080] In order to further study the function of MS33 gene in detail, the inventors of the present invention extracted different organs (roots, stems, leaves and anthers of different developmental stages of wild-type maize plant (inbred line Zheng 58), i.e. sex mother cell stage, quarter Somatic, mononucleate, dinucleate, and mature pollen) RNAs were reverse-transcribed to obtain cDNA, and the expression of MS33 gene in different tissues was detected by fluorescent quantitative PCR. Among them, the primers used to detect MS33 gene are MS33-F and MS33-R; maize Aciton is used as an internal reference, and the detection primers are Actin-F and Actin-R.
[0081] MS33-F: 5'-TCTGCGTCACTGCCATGC-3';
[0082] MS33-R: 5'-CGTCGGAGCTCACCACG-3'.
[0083] Actin-F: 5'-GAGATGCCTGATGGTCAGGTCA-3';
[0084] Actin-R: 5'-AGTTGTACGTGGCCTCATGGAC-3'.
[0085] The results showed that the expression of MS33 gene was higher in...
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