P888The Transition from Primary siRNAs to Amplified Secondary siRNAs that Regulate Chalcone Synthase During Development of Glycine max Seed Coats
The Transition from Primary siRNAs to Amplified Secondary siRNAs that Regulate Chalcone Synthase During Development of Glycine max Seed Coats
Date: Monday, January 13, 2014
Room: Grand Exhibit Hall
The I locus is a 27-kb inverted repeat cluster of chalcone synthase genes CHS1-3-4 that mediates siRNA down-regulation of
CHS7 and CHS8 target mRNAs during seed development leading to yellow seed coats lacking anthocyanin pigments. Here,
we report small RNA sequencing of ten stages of seed development from a few days post fertilization through maturity,
revealing the amplification from primary to secondary short interfering RNAs (siRNAs) occurring during development. The
young seed populations had a higher proportion of siRNAs representing the CHS1-3-4 gene family members, consistent
with this region as the origin of the primary siRNAs. More intriguingly, the very young seed had a higher proportion of 22-nt
CHS siRNAs than did the mid-maturation seed. We infer that the primary CHS siRNAs increase during development to levels
sufficient to trigger amplification of secondary CHS siRNAs from the CHS7/8 target mRNAs, enabling the total levels of 21-nt
CHS siRNAs to rise dramatically. Further, we demonstrate that the soybean system exhibits tissue-specific CHS siRNA
production because primary CHS siRNA levels are not sufficient to trigger secondary amplification in tissues other than the
seed coat.
CHS7 and CHS8 target mRNAs during seed development leading to yellow seed coats lacking anthocyanin pigments. Here,
we report small RNA sequencing of ten stages of seed development from a few days post fertilization through maturity,
revealing the amplification from primary to secondary short interfering RNAs (siRNAs) occurring during development. The
young seed populations had a higher proportion of siRNAs representing the CHS1-3-4 gene family members, consistent
with this region as the origin of the primary siRNAs. More intriguingly, the very young seed had a higher proportion of 22-nt
CHS siRNAs than did the mid-maturation seed. We infer that the primary CHS siRNAs increase during development to levels
sufficient to trigger amplification of secondary CHS siRNAs from the CHS7/8 target mRNAs, enabling the total levels of 21-nt
CHS siRNAs to rise dramatically. Further, we demonstrate that the soybean system exhibits tissue-specific CHS siRNA
production because primary CHS siRNA levels are not sufficient to trigger secondary amplification in tissues other than the
seed coat.
