» Articles » PMID: 33217085

The Emergence and Evolution of Intron-poor and Intronless Genes in Intron-rich Plant Gene Families

Overview
Journal Plant J
Date 2020 Nov 20
PMID 33217085
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Eukaryotic genes can be classified into intronless (no introns), intron-poor (three or fewer introns per gene) or intron-rich. Early eukaryotic genes were mostly intron-rich, and their alternative splicing into multiple transcripts, giving rise to different proteins, might have played pivotal roles in adaptation and evolution. Interestingly, extant plant genomes contain many gene families with one or sometimes few sub-families with genes that are intron-poor or intronless, and it remains unknown when and how these intron-poor or intronless genes have originated and evolved, and what their possible functions are. In this study, we identified 33 such gene families that contained intronless and intron-poor sub-families. Intronless genes seemed to have first emerged in early land plant evolution, while intron-poor sub-families seemed first to have appeared in green algae. In contrast to intron-rich genes, intronless genes in intron-poor sub-families occurred later, and were subject to stronger functional constraints. Based on RNA-seq analyses in Arabidopsis and rice, intronless or intron-poor genes in AP2, EF-hand_7, bZIP, FAD_binding_4, STE_STE11, CAMK_CAMKL-CHK1 and C2 gene families were more likely to play a role in response to drought and salt stress, compared with intron-rich genes in the same gene families, whereas intronless genes in the B_lectin and S_locus_glycop gene family were more likely to participate in epigenetic processes and plant development. Understanding the origin and evolutionary trajectory, as well as the potential functions, of intronless and intron-poor sub-families provides further insight into plant genome evolution and the functional divergence of genes.

Citing Articles

Genome-Wide Identification and Expression Analysis of Transcription Factors Responding to Multiple Stresses in L.

Zhu Y, Niu S, Lin J, Yang H, Zhou X, Wang S Int J Mol Sci. 2025; 26(3).

PMID: 39940846 PMC: 11816611. DOI: 10.3390/ijms26031069.


Analysis of the CHS Gene Family Reveals Its Functional Responses to Hormones, Salinity, and Drought Stress in Moso Bamboo ().

Su S, Xuan X, Tan J, Yu Z, Jiao Y, Zhang Z Plants (Basel). 2025; 14(2).

PMID: 39861515 PMC: 11769273. DOI: 10.3390/plants14020161.


Genome-Wide Identification and Analysis of Transcription Factor Family Genes Involved in Cold Stress Tolerance in Winter Rapeseed ( L.).

Xu Y, Ma L, Zeng X, Xu Y, Tao X, Fahim A Int J Mol Sci. 2025; 25(24.

PMID: 39769355 PMC: 11678751. DOI: 10.3390/ijms252413592.


Genome-wide identification of the ATP-dependent zinc metalloprotease (FtsH) in Triticeae species reveals that TaFtsH-1 regulates cadmium tolerance in Triticum aestivum.

Huang Y, Cao L, Chen T, Chang X, Fang Y, Wu L PLoS One. 2024; 19(12):e0316486.

PMID: 39739686 PMC: 11687710. DOI: 10.1371/journal.pone.0316486.


Genome-Wide Identification of Family Genes in Three Plant Species and Functional Characterization of s in Chinese Kale Under Abiotic Stresses.

Zhao Y, Chen S, Qin M, Shui K, Li R, Yang B Int J Mol Sci. 2024; 25(23).

PMID: 39684617 PMC: 11641214. DOI: 10.3390/ijms252312907.


References
1.
LARKIN M, Blackshields G, Brown N, Chenna R, McGettigan P, McWilliam H . Clustal W and Clustal X version 2.0. Bioinformatics. 2007; 23(21):2947-8. DOI: 10.1093/bioinformatics/btm404. View

2.
Liu Z, Qin J, Tian X, Xu S, Wang Y, Li H . Global profiling of alternative splicing landscape responsive to drought, heat and their combination in wheat (Triticum aestivum L.). Plant Biotechnol J. 2017; 16(3):714-726. PMC: 5814593. DOI: 10.1111/pbi.12822. View

3.
Lang D, Ullrich K, Murat F, Fuchs J, Jenkins J, Haas F . The Physcomitrella patens chromosome-scale assembly reveals moss genome structure and evolution. Plant J. 2017; 93(3):515-533. DOI: 10.1111/tpj.13801. View

4.
Roy S, Gilbert W . Rates of intron loss and gain: implications for early eukaryotic evolution. Proc Natl Acad Sci U S A. 2005; 102(16):5773-8. PMC: 556292. DOI: 10.1073/pnas.0500383102. View

5.
Finn R, Bateman A, Clements J, Coggill P, Eberhardt R, Eddy S . Pfam: the protein families database. Nucleic Acids Res. 2013; 42(Database issue):D222-30. PMC: 3965110. DOI: 10.1093/nar/gkt1223. View