Genome-Wide Reidentification and Expression Analysis of MADS-Box Gene Family in Cucumber

MADS-box transcription factors play a crucial role in plant growth and development. Although previous genome-wide analyses have investigated the MADS-box family in cucumber, this study provides the first comprehensive reannotation of the <i>MADS-box</i> gene family in <i>Cucumis sativus</i> using updated Cucurbitaceae genome data, offering novel insights into the gene family's evolution and functional diversity. The results show that a total of 48 <i>CsMADS-box</i> genes were identified in the V3 version of cucumber, while 3 of the 43 genes identified in the V1 version were duplicated. The V1 version actually has only 40 genes. Additionally, we analyzed the variability in protein sequences and found that the amino acid sequences of 14 genes showed no differences between the two versions of the database, while the amino acid sequences of 29 genes exhibited significant differences. The further analysis of conserved motifs revealed that although the amino acid lengths of 15 genes had changed, their conserved motifs remained unchanged; however, the conserved motifs of 12 genes had altered. Furthermore we found that motif1 and motif2 were present in most proteins, indicating that they are highly conserved. Gene structure analysis revealed that most type I (Mα, Mβ) <i>MADS-box</i> genes lack introns, whereas type II (MIKC) genes exhibit a similar structure with a higher number of introns. Chromosomal localization analysis indicated that <i>CsMADS-box</i> genes are unevenly distributed across the seven chromosomes of cucumber. Promoter region analysis showed that the promoter regions of <i>CsMADS-box</i> genes contain response elements related to plant growth and development, suggesting that <i>CsMADS-box</i> genes may be extensively involved in plant growth and development. Different <i>CsMADS-box</i> genes exhibit specific high expression in roots, stems, leaves, tendrils, male flowers, female flowers, and ovaries, suggesting that these genes play crucial roles in the growth, development, reproduction and morphogenesis of cucumber. Moreover, 26, 18, 8, and 10 <i>CsMADS-box</i> genes were differentially expressed under high temperature, NaCl and/or silicon, downy mildew, and powdery mildew treatments, respectively. Interestingly, <i>CsMADS07</i> and <i>CsMADS16</i> responded to all tested stress conditions. These findings provide a reference and basis for further investigation into the function and mechanisms of the <i>MADS-box</i> genes for resistance breeding in cucumber.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-04-17
DOI
https://doi.org/10.3390/ijms26083800
Citations
1
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
1.75

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article

Genome-Wide Reidentification and Expression Analysis of MADS-Box Gene Family in Cucumber

Zimo Wang, Zhonghai Ren, Lina Wang, Xuehua Wang et al.
1 citations
International Journal of Molecular Sciences
Plant Molecular Biology Research
1.75
article

Genome-Wide Reidentification and Expression Analysis of MADS-Box Gene Family in Cucumber

Zimo Wang, Zhonghai Ren, Lina Wang, Xuehua Wang, Mengmeng Yin, Jing Han, Jingshu Chang
article en
1 citations

Abstract

MADS-box transcription factors play a crucial role in plant growth and development. Although previous genome-wide analyses have investigated the MADS-box family in cucumber, this study provides the first comprehensive reannotation of the <i>MADS-box</i> gene family in <i>Cucumis sativus</i> using updated Cucurbitaceae genome data, offering novel insights into the gene family's evolution and functional diversity. The results show that a total of 48 <i>CsMADS-box</i> genes were identified in the V3 version of cucumber, while 3 of the 43 genes identified in the V1 version were duplicated. The V1 version actually has only 40 genes. Additionally, we analyzed the variability in protein sequences and found that the amino acid sequences of 14 genes showed no differences between the two versions of the database, while the amino acid sequences of 29 genes exhibited significant differences. The further analysis of conserved motifs revealed that although the amino acid lengths of 15 genes had changed, their conserved motifs remained unchanged; however, the conserved motifs of 12 genes had altered. Furthermore we found that motif1 and motif2 were present in most proteins, indicating that they are highly conserved. Gene structure analysis revealed that most type I (Mα, Mβ) <i>MADS-box</i> genes lack introns, whereas type II (MIKC) genes exhibit a similar structure with a higher number of introns. Chromosomal localization analysis indicated that <i>CsMADS-box</i> genes are unevenly distributed across the seven chromosomes of cucumber. Promoter region analysis showed that the promoter regions of <i>CsMADS-box</i> genes contain response elements related to plant growth and development, suggesting that <i>CsMADS-box</i> genes may be extensively involved in plant growth and development. Different <i>CsMADS-box</i> genes exhibit specific high expression in roots, stems, leaves, tendrils, male flowers, female flowers, and ovaries, suggesting that these genes play crucial roles in the growth, development, reproduction and morphogenesis of cucumber. Moreover, 26, 18, 8, and 10 <i>CsMADS-box</i> genes were differentially expressed under high temperature, NaCl and/or silicon, downy mildew, and powdery mildew treatments, respectively. Interestingly, <i>CsMADS07</i> and <i>CsMADS16</i> responded to all tested stress conditions. These findings provide a reference and basis for further investigation into the function and mechanisms of the <i>MADS-box</i> genes for resistance breeding in cucumber.

International Journal of Molecular SciencesVol. 26(8)
Liaocheng University (CN), Shandong Agricultural University (CN)
National Natural Science Foundation of China, Agricultural Variety Improvement Project of Shandong Province, Government of Shandong Province
Life in Land
Openalex Percentile: Top 16%
Plant Molecular Biology Research
1.75
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