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Acta Agronomica Sinica ›› 2023, Vol. 49 ›› Issue (4): 893-905.doi: 10.3724/SP.J.1006.2023.24065

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

BnABCI8 affects chloroplast development of Brassica napus

CHEN Xiao-Han(), WANG Li-Qin, WANG Hua-Dong, XIAO Qing, TAO Bao-Long, ZHAO Lun, WEN Jing, YI Bin, TU Jin-Xing, FU Ting-Dong, SHEN Jin-Xiong()   

  1. National Key Laboratory of Crop Genetic Improvement/National Engineering Research Center of Rapeseed, Huazhong Agricultural University, Wuhan 430070, Hubei, China
  • Received:2022-03-23 Accepted:2022-07-21 Online:2023-04-12 Published:2022-08-01
  • Contact: SHEN Jin-Xiong E-mail:809365931@qq.com;jxshen@mail.hzau.edu.cn
  • Supported by:
    National Natural Science Foundation of China(31930032)

Abstract:

Mature chloroplast is an important place for photosynthesis of higher plants and important organs that affects crop yield. BnABCI8 is a member of the ABC transporter I subfamily, and there are two functional copies of BnA09.ABCI8 and BnC09.ABCI8 in Brassica napus. Their amino acid sequences are very conserved in different species. The relative expression patterns showed that BnABCI8 was expressed in all tissues of Brassica napus, and the relative expression level in leaves and flowers was higher. Subcellular localization indicated that BnABCI8 was located in chloroplast. Phenotypic identification showed that the double mutation of BnA09.ABCI8 and BnC09.ABCI8 and the single mutation of BnA09.ABCI8 both resulted in yellow cotyledons and chlorotic true leaves, among which double mutant was more severe chlorosis. Transmission electron microscope demonstrated that the chloroplasts in the double mutants could not form normal thylakoid membranes. The knock-out of BnABCI8 resulted in the decrease of the relative expression level of related genes in the chlorophyll synthesis pathway, and significantly increased the iron content in mutant leaves. These results indicated that the mutation of BnABCI8 resulted in abnormal chloroplast structure, hindered the synthesis of chlorophyll, and significantly increased the iron content in the leaves. In addition, the accumulation of iron ion might lead to a series of reactions such as accumulation of reactive oxygen species, cell death and chlorophyll degradation, and eventually led to mutation of leaf color.

Key words: Brassica napus, BnABCI8 gene, ABC transporter, chloroplast development, chlorophyll synthesis, variegated mutant

Table S1

Primers used in this study"

引物名称
Primer name
引物序列
Primer sequence (5'-3')
作用
Function
C83-A09F cttgcatgcctgcaggtcgacATGGCGTCTCTCCTCGCG 亚细胞定位
Subcellular localization assay
C83-A09R tctaccggtacccggggatccGAACCCACTGATCCTTCAAGCTT
C83-C09FF cttgcatgcctgcaggtcgacATGGCGTCTCTCCTCGCG
C83-C09RR tctaccggtacccggggatccGAACCCACTGATCCTTCAAGCTT
C83F ATTTCATTTGGAGAGGACCTCG
C83R TGTGCCCATTAACATCACCATC
QA09F ATCCAGGTTAAGAATCCATCAGCG qPCR
分析
qPCR
analysis
QA09R TCTGCAGAACCCTGAGATCATCG
QC09F ATCCAGGTTAAGAACCCATCAGCC
QC09R TCTGCAGAACCCAGAGATCATTG
QHEMA1F TCCGAGGAACAACAACAGAACCAG
QHEMA1R TGTATATCTGTCGGGTGCAGAGT
QHEMCF CGGTTCCGTCTCCGTCAT
QHEMCR GGCATTAGGTGCGGATTCAG
QHEME2F CGAAATCTTCCCGGTCAATTCGTTG
QHEME2R AGAGGCTCAGTGGTTGCAGAG
QCHLHF GCACGCTTGGTTTGCATCCTATT
QCHLHR CATGTGACTTCCCTGTTCTAGGGTCA
QCHLDF GATTGCTATTTCAGGTCGTAGAGG
引物名称
Primer name
引物序列
Primer sequence (5'-3')
作用
Function
QCHLDR GTTCGTCTTCCCACTCATCAG
QCHLMF GCGACGATCGTTTCCTTGAC
QCHLMR AAATACTCCCTCACCACCTCCTT
QDVRF TCCAGTGGATACATACAACCAATGGCT
QDVRR ATTGGTTTGGAAGGTGGAAGCGAGA
QPORCF CCGACAAGATCTCCATCAAGGAG
QPORCR CGGCGATGCTTCGTTCGAT
QCHLGF CGAGTTGGAGCACTCTCTCTCCA
QCHLGR CTCTTCCCAGAAGAGTTGGAGTCC
QCAOF GTCTATTGTCTTCCTTCTTCCTC
QCAOR TCCTTTCACTCCCTTCTTTCTG
actionQ3F CTATCCTCCGTCTCGATCTCGC
actionQ3R CTTAGCCGTCTCCAGCTCTTGC
HA09-1-F ggagtgagtacggtgtgcACAGTACTTCCAAAACCTAGACTACGAC Hi-tom
分析
Hi-tom analysis
HA09-1-R gagttggatgctggatggGCCGAGCTTGTCGAAATACTCGA
HA09-2-F ggagtgagtacggtgtgcCCGCTTTGAACTCAGCTGTGT
HA09-2-R gagttggatgctggatggCTTCGTGACGAAATTATAAATCCCTCCT
HC09-1-F ggagtgagtacggtgtgcGCAATACTTCCAAAACCTAGACTACGAC
HC09-1-R gagttggatgctggatggGCCGAGCTTGTCGAAGTAGTCAA
HC09-2-F ggagtgagtacggtgtgcCTGCTCTGAACTCCGCCG
HC09-2-R gagttggatgctggatggGTGACGAAATTGTAGATCCCTCCCTTC
F-1 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttGCGTtggagtgagtacggtgtgc
F-2 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttGTAGtggagtgagtacggtgtgc
F-3 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttACGCtggagtgagtacggtgtgc
F-4 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttCTCGtggagtgagtacggtgtgc
F-5 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttGCTCtggagtgagtacggtgtgc
F-6 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttAGTCtggagtgagtacggtgtgc
F-7 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttCGACtggagtgagtacggtgtgc
F-8 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttGATGtggagtgagtacggtgtgc
F-9 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttATACtggagtgagtacggtgtgc
F-10 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttCACAtggagtgagtacggtgtgc
F-11 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttGTGCtggagtgagtacggtgtgc
F-12 ACTCTTTCCCTACACGACGCTCTTCCGATCTgcttACTAtggagtgagtacggtgtgc
R-A GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtGCGTtgagttggatgctggatgg
R-B GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtGTAGtgagttggatgctggatgg
R-C GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtACGCtgagttggatgctggatgg
R-D GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtCTCGtgagttggatgctggatgg
R-E GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtGCTCtgagttggatgctggatgg
R-F GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtAGTCtgagttggatgctggatgg
R-G GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtCGACtgagttggatgctggatgg
R-H GACTGGAGTTCAGACGTGTGCTCTTCCGATCTctgtGATGtgagttggatgctggatgg
5UDI427 AATGATACGGCGACCACCGAGATCTACACGCCTTCAAACACTCTTTCCCTACACGACGC
5UDI428 AATGATACGGCGACCACCGAGATCTACACAGGAACCTACACTCTTTCCCTACACGACGC
7UDI427 CAAGCAGAAGACGGCATACGAGATTCACGAAGGTGACTGGAGTTCAGACGTGTGCTCTT
引物名称
Primer name
引物序列
Primer sequence (5'-3')
作用
Function
7UDI428 CAAGCAGAAGACGGCATACGAGATCTTAGCCAGTGACTGGAGTTCAGACGTGTGCTCTT
Cas9F CGAGAAGAAGAACGGCCTGTTCG 基因编辑
Gene editing
Cas9R AGTTGCCCCTAGCGAGTGGG
U626-IDF TGTCCCAGGATTAGAATGATTAGGC
U629-IDR AGCCCTCTTCTTTCGATCCATCAAC
crp1-BsF-ABCI8 ATATATGGTCTCGATTGACTCCTTCACAATCCCCAAGTT
crp1-F0-ABCI8 TGACTCCTTCACAATCCCCAAGTTTTAGAGCTAGAAATAGC
crp2-R0-ABCI8 AACCGTGTTCTTGGGGATATAGCAATCTCTTAGTCGACTCTAC
crp2-BsR-ABCI8 ATTATTGGTCTCGAAACCGTGTTCTTGGGGATATAGCAA

Fig. 1

Relationship among ABCI8 orthologs in plants A: the phylogenetic tree of the sequence of BnABCI8 and its putative orthologs in different species. Numbers on branches are bootstrap values for 1000 replications. B: the amino acid sequences of BnABCI8 and putative orthologs in five species."

Fig. 2

Relative expression pattern of BnABCI8 genes Values are means ± SDs (n = 3)."

Fig. 3

Subcellular localization of BnABCI8 A, E: green fluorescence signals of transformed tobacco with the P35S::BnaA09.ABCI8:GFP and P35S::BnaC09.ABCI8:GFP constructs, respectively. B, F: red fluorescence of chloroplasts in tobacco. C, G: the image under bright field. D, H: the merged images from (A-C) and (E-G), respectively."

Fig. 4

Gene structure of BnABCI8 and plant identification of CRISPR-edited positive plants A: gene structure of BnA09.ABCI8 and BnC09.ABCI8; B: the electrophoretic identification of CRISPR-edited positive plants. The marker bands are 2 kb, 1 kb, 750 bp, 500 bp, and 200 bp, respectively, and the target band is 686 bp."

Fig. 5

Identification of T1 generation mutant A: the editing of some plants. The yellow mark indicates the PAM site and the inserted base, and the red dash indicates the deletion. B: the relative expression levels of BnABCI8 in mutants. * and ** mean significant differences at P < 0.05 and P < 0.01, respectively."

Fig. 6

Phenotypic observation of cotyledons in mutants A-C: 10-day-old wild type; D-F: 10-day-old single mutants; G-I: 10-day-old double mutants; J-L: 17-day-old double mutants."

Fig. 7

Phenotypic observation of mutants A: 56-day-old wild type; B: 56-day-old single mutants; C: 56-day-old double mutants."

Fig. 8

Phenotypic observation and chlorophyll content determination of true leaf in double mutant A, C: the comparison of true leaves and chlorophyll contents between double mutant and WT at 30 days old; B, D: the comparison of true leaves and chlorophyll contents between double mutant and WT at 56 days old. Values are presented as mean ± SD (n = 3). * and ** mean significant differences at P < 0.05 and P < 0.01, respectively."

Fig. 9

Relative expression levels of genes related to the chlorophyll synthesis pathway Value is mean ± SD (n = 3). * and ** mean significant differences at P < 0.05 and P < 0.01, respectively."

Fig. 10

Fe content in leaves a09 represents single mutants of the BnA09.ABCI8; a09 c09 represents double mutants of the BnA09.ABCI8 and BnC09.ABCI8. Value is mean ± SD (n = 3). * and ** mean significant differences at P < 0.05 and P < 0.01, respectively."

Fig. 11

Chloroplast ultrastructure of double mutant and WT A-C: the chloroplast structure of wild type; D-F: the chloroplast structure of double mutant; Cp: chloroplast; Tm: thylakoid membrane."

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