Skip to main content
Log in

Nucleo-cytoplasmic interactions affect the 5’ terminal transcription of mitochondrial genes between the isonuclear CMS line UG93A and its maintainer line UG93B of kenaf (Hibiscus cannabinus)

  • Original Article
  • Published:
Development Genes and Evolution Aims and scope Submit manuscript

Abstract

Gene expression and translation in plant mitochondria remain poorly understood due to the complicated transcription of its mRNA. In this study, we report the 5’ and 3’ RNA extremities and promoters of five mitochondrial genes, atp1, atp4, atp6, atp9, and cox3. The results reveal that four genes (atp1, atp4, atp6, and cox3) are transcribed from multiple initiation sites but with a uniform transcript at the 3’ end, indicating that heterogeneity of the 5’ end is a common feature in the transcription of kenaf mitochondrial genes. Furthermore, we found that the transcription initiation sites of these four genes are significantly different in UG93A, UG93B, and the F1 hybrid. These data indicate that nuclear loci and unknown transcription factors within the mitochondria of different cytoplasmic types may be involved in mitochondrial transcription. Promoter architecture analysis showed that the promoter core sequences are conserved in the kenaf mitochondrial genome but are highly divergent, suggesting that these elements are essential for the promoter activity of mitochondrial genes in kenaf. Our results reveal that the heterogeneity of the 5’ end and uniformity at the 3’ end are common transcriptional features of mitochondrial genes. These data provide essential information for understanding the transcription of mitochondrial genes in kenaf and can be used as a reference for other plants.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Data availability

All data generated or analyzed during this study are included in the published article and its supplementary information files.

References

Download references

Funding

This study was supported by the National Natural Science Foundation of China (31571719), managed by Ruiyang Zhou; the National Natural Science Foundation of China (31660430), managed by Yanhong Zhao; the Natural Science Foundation of Guangxi Province (2018JJB130045, 2019JJA130200, and 2020JJA130114); and the Basic Business Expenses Project of Guangxi Academy of Agricultural Sciences (No. Guinongke2019M23), managed by Xiaofang Liao.

Author information

Authors and Affiliations

Authors

Contributions

R. Z. conceived the experiment. X. L. conducted the experiment and drafted the manuscript. H. L. and B. Z. isolated the kenaf RNA. W. H. and X. T assisted with the experiment. A. K. and F. M. revised the manuscript, and Y. Z. provided suggestions and edits for the manuscript.

Corresponding author

Correspondence to Ruiyang Zhou.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Statement

This article is present on a university repository website/archive and can be accessed at https://www.biorxiv.org/content/biorxiv/early/2019/01/17/523647.full.pdf. This article is not published nor is it under consideration for publication elsewhere.

Additional information

Communicated by Yves Deveaux.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Liao, X., Li, H., Khan, A. et al. Nucleo-cytoplasmic interactions affect the 5’ terminal transcription of mitochondrial genes between the isonuclear CMS line UG93A and its maintainer line UG93B of kenaf (Hibiscus cannabinus). Dev Genes Evol 231, 119–130 (2021). https://doi.org/10.1007/s00427-021-00682-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00427-021-00682-z

Keywords

Navigation