Background. The same species of plant can exhibit very diverse sizes and shapes of organs that are genetically determined. Characterising genetic variation underlying this morphological diversity is an important objective in evolutionary studies and it also helps identify the functions of genes influencing plant growth and development. Extensive screens of mutagenised Arabidopsis populations have identified multiple genes and mechanisms affecting organ size and shape, but relatively few studies have exploited the rich diversity of natural populations to identify genes involved in growth control.
Results. We screened a relatively well characterised collection of Arabidopsis thaliana accessions for variation in petal size. Association analyses identified sequence and gene expression variation on chromosome 4 that made a substantial contribution to differences in petal area. Variation in the expression of a previously uncharacterised gene At4g16850 (named as KSK) had a substantial role on variation in organ size by influencing cell size. Over-expression of KSK led to larger petals with larger cells and promoted the formation of stamenoid features. The expression of auxin-responsive genes known to limit cell growth was reduced in response to KSK over-expression. ANT expression was also reduced in KSK over-expression lines, consistent with altered floral identities. Auxin responses were reduced in KSK over-expressing cells, consistent with changes in auxin-responsive gene expression. KSK may therefore influence auxin responses during petal development.
Conclusions. Understanding how genetic variation influences plant growth is important for both evolutionary and mechanistic studies. We used natural populations of Arabidopsis thaliana to identify sequence variation in a promoter region of Arabidopsis accessions that mediated differences in the expression of a previously uncharacterised membrane protein. This variation contributed to altered auxin responses and cell size during petal growth.

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This is a list of supplementary files associated with this preprint. Click to download.
Additional File 1: List of Arabidopsis thaliana accessions used in the GWAS analysis.
Additional File 2: Petal phenotype data.
Additional File 3: Representative petals from the Swedish accessions.
Additional File 4: Q-RT-PCR analysis of At4g16850 in seedlings of Col-0, Dju-1, T880 and T1070.
Additional File 5: Promoter alignments of the Dju-1 and Col-0 KSK genes.
Additional File 6: Organ counts in Col-0 and 35S::KSK flowers.
Additional File 7: Primer sequences used in this study.
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Posted 21 Oct, 2020
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On 31 Jan, 2020
On 30 Jan, 2020
Invitations sent on 29 Jan, 2020
On 17 Jan, 2020
On 16 Jan, 2020
On 16 Jan, 2020
On 14 Jan, 2020
Posted 21 Oct, 2020
On 14 Oct, 2020
On 13 Oct, 2020
On 02 Oct, 2020
On 28 Sep, 2020
On 27 Sep, 2020
On 27 Sep, 2020
Received 17 Sep, 2020
On 17 Sep, 2020
On 14 Sep, 2020
Received 14 Sep, 2020
Invitations sent on 11 Sep, 2020
On 11 Sep, 2020
On 27 Aug, 2020
On 26 Aug, 2020
On 26 Aug, 2020
On 13 Feb, 2020
Received 12 Feb, 2020
On 03 Feb, 2020
Received 31 Jan, 2020
On 31 Jan, 2020
On 30 Jan, 2020
Invitations sent on 29 Jan, 2020
On 17 Jan, 2020
On 16 Jan, 2020
On 16 Jan, 2020
On 14 Jan, 2020
Background. The same species of plant can exhibit very diverse sizes and shapes of organs that are genetically determined. Characterising genetic variation underlying this morphological diversity is an important objective in evolutionary studies and it also helps identify the functions of genes influencing plant growth and development. Extensive screens of mutagenised Arabidopsis populations have identified multiple genes and mechanisms affecting organ size and shape, but relatively few studies have exploited the rich diversity of natural populations to identify genes involved in growth control.
Results. We screened a relatively well characterised collection of Arabidopsis thaliana accessions for variation in petal size. Association analyses identified sequence and gene expression variation on chromosome 4 that made a substantial contribution to differences in petal area. Variation in the expression of a previously uncharacterised gene At4g16850 (named as KSK) had a substantial role on variation in organ size by influencing cell size. Over-expression of KSK led to larger petals with larger cells and promoted the formation of stamenoid features. The expression of auxin-responsive genes known to limit cell growth was reduced in response to KSK over-expression. ANT expression was also reduced in KSK over-expression lines, consistent with altered floral identities. Auxin responses were reduced in KSK over-expressing cells, consistent with changes in auxin-responsive gene expression. KSK may therefore influence auxin responses during petal development.
Conclusions. Understanding how genetic variation influences plant growth is important for both evolutionary and mechanistic studies. We used natural populations of Arabidopsis thaliana to identify sequence variation in a promoter region of Arabidopsis accessions that mediated differences in the expression of a previously uncharacterised membrane protein. This variation contributed to altered auxin responses and cell size during petal growth.

Figure 1

Figure 2

Figure 3

Figure 4

Figure 5

Figure 6
This is a list of supplementary files associated with this preprint. Click to download.
Additional File 1: List of Arabidopsis thaliana accessions used in the GWAS analysis.
Additional File 2: Petal phenotype data.
Additional File 3: Representative petals from the Swedish accessions.
Additional File 4: Q-RT-PCR analysis of At4g16850 in seedlings of Col-0, Dju-1, T880 and T1070.
Additional File 5: Promoter alignments of the Dju-1 and Col-0 KSK genes.
Additional File 6: Organ counts in Col-0 and 35S::KSK flowers.
Additional File 7: Primer sequences used in this study.
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