Abstract

Naturally occurring mutants whose phenotype recapitulates the changes that distinguish closely related species are of special interest from the evolutionary point of view. They can give a key about the genetic control of the changes that led to speciation. In this study, we described lepidium-like (lel), a naturally occurring variety of an allotetraploid species Capsella bursa-pastoris that is characterized by the typical loss of all four petals. In some cases, one or two basal flowers in the raceme had one or two small petals. The number and structure of other floral organs are not affected. Our study of flower development in the mutant showed that once initiated, petals either cease further development and cannot be traced in anthetic flowers or sometimes develop to various degrees. lel plants showed an earlier beginning of floral organ initiation and delayed petal initiation compared to the wild-type plants. lel phenotype has a wide geographical distribution, being found at the northern extremity of the species range as well as in the central part. The genetic analysis of inheritance demonstrated that lel phenotype is controlled by two independent loci. While the flower in the family Cruciferae generally has a very stable structure (i.e., four sepals, four petals, six stamens, and two carpels), several deviations from this ground plan are known, in particular in the genus Lepidium, C. bursa-pastoris is an emerging model for the study of polyploidy (which is also very widespread in Cruciferae); the identification and characterization of the apetalous mutant lays a foundation for further research of morphological evolution in polyploids.

Highlights

  • An important feature of many angiosperm flowers is the occurrence of structures serving for the attraction of pollinators and protection of reproductive organs

  • We discovered a novel natural mutant of C. bursa-pastoris in Moscow, Russia, and named it lel since its flowers resemble those of some species of the genus Lepidium in the typical absence of visible petals

  • As we have identified the recessive mode of inheritance of apetaly in locus 2, we analyzed A. thaliana orthologs of four C. bursa-pastoris genes harboring premature stop codons: genes AT1G29230 (CBLINTERACTING PROTEIN KINASE 18) encoding a member of the SNF1-related kinase gene family, AT1G23210 (GLYCOSYL HYDROLASE 9B6), AT1G26410 (ATBBE6) where the product belonged to the flavin adenine dinucleotide (FAD)-binding Berberine family, and AT1G26640 (ISOPENTENYL PHOSPHATE KINASE) encoding an isopentenyl phosphate kinase that regulates terpenoid compounds

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Summary

Introduction

An important feature of many angiosperm flowers is the occurrence of structures serving for the attraction of pollinators and protection of reproductive organs. Petal Loss Evolution in Cruciferae and corolla is a key innovation of eudicots. Sepals and petals (as well as nectaries) do not directly influence plant viability and fertility, and these organs are in certain sense optional in floral morphology (Irish, 2008). A loss of petals is widespread across eudicots. Can emerge as a homeotic transformation of petals into other organs such as stamens, petal loss, or petal suppression. These phenomena can affect all or only some petals of a flower. The recurrent loss of petals considerably increases the variation of flower ground plan (Endress, 2006; Pieper et al, 2016). Apart from wind-pollinated lineages, apetaly is especially common among selfing plants since they do not require pollinators (Culley and Klooster, 2007; Sharples et al, 2021)

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