Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
Plants usually respond to the external environment by initiating a series of signal transduction processes mediated by protein kinases, especially calcineurin B-like protein–interacting protein kinases (CIPKs). In this study, 54 CIPKs were identified in the peanut genome, of which 26 were from culti...
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Veröffentlicht in: | Frontiers in genetics 2022-09, Vol.13, p.939255-939255 |
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Zusammenfassung: | Plants usually respond to the external environment by initiating a series of signal transduction processes mediated by protein kinases, especially calcineurin B-like protein–interacting protein kinases (CIPKs). In this study, 54
CIPKs
were identified in the peanut genome, of which 26 were from cultivated species (named
AhCIPKs
) and 28 from two diploid progenitors (
Arachis duranensis—AdCIPKs
and
Arachis ipaensis—AiCIPKs
). Evolution analysis revealed that the 54
CIPKs
were composed of two different evolutionary branches. The
CIPK
members were unevenly distributed at different chromosomes. Synteny analysis strongly indicated that whole-genome duplication (allopolyploidization) contributed to the expansion of
CIPK
. Comparative genomics analysis showed that there was only one common collinear
CIPK
pairs among peanut,
Arabidopsis
, rice, grape, and soybean. The prediction results of
cis
-acting elements showed that
AhCIPKs
,
AdCIPKs
, and
AiCIPKs
contained different proportions of transcription factor binding motifs involved in regulating plant growth, abiotic stress, plant hormones, and light response elements. Spatial expression profiles revealed that almost all
AhCIPKs
had tissue-specific expression patterns. Furthermore, association analysis identified one polymorphic site in
AdCIPK12
(
AhCIPK11
), which was significantly associated with pod length, seed length, hundred seed weight, and shoot root ratio. Our results provide valuable information of
CIPKs
in peanut and facilitate better understanding of their biological functions. |
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ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2022.939255 |