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Acta Agronomica Sinica ›› 2023, Vol. 49 ›› Issue (9): 2362-2372.doi: 10.3724/SP.J.1006.2023.22062

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

Mutation effects of OsCDF1 gene and its genomic variations in rice

HU Yan-Juan(), XUE Dan, GENG Di, ZHU Mo, WANG Tian-Qiong, WANG Xiao-Xue()   

  1. Rice Research Institute, Shenyang Agricultural University, Shenyang 110866, Liaoning, China
  • Received:2022-10-28 Accepted:2023-02-21 Online:2023-09-12 Published:2023-03-16
  • Supported by:
    National Key Research and Development Program of China(2017YFD0300107);National Natural Science Foundation of China(32070642)

Abstract:

Flowering time (heading date) affects yield, quality, and regional adaptability of rice. The Cycling DOF Factor 1 (CDF1) protein is a transcriptional repressor of CONSTANS (CO) and negatively regulates flowering time in Arabidopsis. However, the biological functions of OsCDF1 in rice is not quite clear. To explore the biological functions of OsCDF1 and its effects on flowering time control in rice, we constructed two binary vectors carrying guide RNAs targeting OsCDF1 gene via CRISPR/Cas9 system. The resultant plasmids were transferred into SN9816 which was the variety widely cultivated in northern China by using an Agrobacterium-mediated transformation, and the mutations of OsCDF1 was firstly generated in SN9816. The flowering time and yield related traits of SN9816 and oscdf1 mutants were investigated in the paddy field. The main results were as follows: Two homozygous oscdf1 lines were identified, including a five bp deletion at 16th bp of the first exon and a single base pair A insertion at 338th bp of the second exon. Sequence alignment analysis revealed that the two types of mutations resulted in frame-shift and premature translation termination. Mutations of OsCDF1 delayed flowering time, but increased yield under natural long day conditions in rice. Analysis of OsCDF1 genetic variations and haplotype networks revealed that the rice accessions had evolved high genomic diversity in OsCDF1 locus. The knockout mutants of OsCDF1 created by CRISPR/Cas9 provided the theoretical basis to further study the role of OsCDF1 gene in rice and the potential gene and germplasm resources for genetic improvement in rice.

Key words: rice, CRISPR/Cas9, OsCDF1, flowering time, yield related traits, haplotype

Table 1

Primers used in this study"

引物名称
Primer name
正向引物
Forward sequence (5'-3')
反向引物
Reverse sequence (5'-3')
OsCDF1gR1 ggcaGGGGAGTGCAAGGTGGGAGG aaacCCTCCCACCTTGCACTCCCC
OsCDF1gR2 ggcaGTGCCCCCGGTGTAGCAGCA aaacTGCTGCTACACCGGGGGCAC
gR ATTTCGTAGTGGGCCATGAA TAGTCCGTTTTTAGCGCGTG
Hyg GTGCTTGACATTGGGGAGTT GATGTTGGCGACCTCGTATT
JCDF1 gR1 TCGTCTCCGGGAGGAGTAGT GATGTGGCGATCGGAATTAG
JCDF1 gR2 GACACCGAGGACTCTTCAGC CTCCTCTCTATGCCCCAGTG
OsACT1 CTATGTTCCCTGGCATTGCT GGCGATAACAGCTCCTCTTG
OsCDF1re AACTACAACATCAACCAGCCG TGAGAACGGTGCCATTAGTCT

Fig. 1

Schematic diagram of OsCDF1 gRNA target sites and screening for positive clones containing the gRNAs of OsCDF1 A: OsCDF1 target site in schematic diagram. The grey, blue rectangles, and black lines represent 5' or 3' UTRs, exons and introns, respectively. Bar: 200 bp. PAM: protospacer adjacent motif. The sequences underlined indicate PAM sequences. B: the amplification of the fragments containing gRNAs in pRGEB32 vector by PCR. M: DNA marker III; 1-2: PCR products. C: the sequencing results of the positive clones containing gRNAs of OsCDF1."

Fig. 2

Screening and analysis of oscdf1 homozygous mutants without T-DNA A: PCR amplification of Hyg fragments. M: DNA marker III; 1-48: PCR products; 1: template is ddH2O. B: mutation type analysis in T1 generation. C: the mutation type analysis in T2 generation. Red arrows show the mutation sites. D: the change of the target sites. The grey, blue rectangles, and black lines represent 5' or 3' UTRs, exons, and introns, respectively. PAM: protospacer adjacent motif. The sequences underlined represent PAM. Bar: 200 bp."

Fig. 3

Schematic representations of amino acid sequence change and tertiary structure analysis of OsCDF1 mutant proteins A: the amino acid change of the target sites. Bar: 50 aa. B: the blast analysis of the mutant proteins. C: the tertiary structure."

Fig. 4

Flowering time phenotype of oscdf1 mutants A: phenotype of oscdf1 mutants. Bar: 10 cm in white line. B: flowering time of oscdf1 mutants (n ≥ 15). *: P < 0.05."

Fig. 5

Comparison of agronomic traits between oscdf1 mutants and wild-type grown in paddy field A: the morphology of panicle between WT and oscdf1 mutant; B: the morphology of branch between WT and oscdf1 mutant; C: panicle number; D: panicle length; E: primary branch number; F: secondary branch number; G: grain length. H: grain width; I: grain length; J: grain width; K: grain thickness; L: the filled grain number per panicle; M: seed-setting rate; N: 1000-grain weight; O: yield weight per plant. Data in C-F and I-J are means ± SDs (n ≥ 15). *: P < 0.05; **: P < 0.01; n.s.: no significant difference."

Fig. 6

Expression pattern of the OsCDF1 gene A: tissue-specific analysis of OsCDF1. B: the relative expression level of OsCDF1 different developmental stages. Data in A and B are means ± SDs."

Fig. 7

Genetic variation and haplotype network analysis of OsCDF1 A: OsCDF1 gene structure and location of the six genomic variations. Black rectangles represent the two exons; Grey rectangles represent the five' untranslated region (5' UTR) and 3' UTR; Black lines represent the intron. B: RFT1 protein structure and location of the six genomic variations. Triangles in different colors indicate the locations of the genetic variations. C: the haplotype network of the six genomic variations. The red lines represent the number of mutations between two haplotypes."

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