13. Uluslararası Ankara Bilimsel Araştırmalar Kongresi, Ankara, Türkiye, 1 - 03 Mart 2026, ss.1-2, (Özet Bildiri)
ABSTRACT
N6-Methyladenosine (m6A) is a conserved and
reversible epigenetic mark involved in the regulation of RNA stability,
translation, and alternative splicing, and is associated with development and
stress responses; it is frequently linked to stress-related pathways,
photosynthesis, and circadian/light signaling. In tea plants, m6A
modifications have been mapped at the transcriptome level through
MeRIP-seq–based studies; these studies demonstrated that modifications are
predominantly enriched near the stop codon and within 3′UTR regions, and that
the canonical RRACH motif is dominant. In addition, differential m6A
peaks have been identified under solar-withering and stress conditions; m6A
regulatory genes such as CsALKBH4
have been reported to affect the stability and alternative splicing of
transcripts associated with flavonoid and terpene biosynthesis. However,
systematic modeling of motif architecture against the genomic average within
specific gene sets has not been performed. In this study, the motif
architecture of RRACH, GGAU, and U-rich elements was examined in PAL, CHS,
DFR, ANS, ANR, and FLS genes
belonging to the phenylpropanoid and flavonoid biosynthesis pathways, as well
as in GS, GOGAT, and GDH genes
involved in nitrogen metabolism. Motif scanning was performed in the R statistical
environment using regex-based algorithms, and motif densities were normalized
per kilobase. The obtained values were compared with genome-wide averages of
tea and modeled multivariately using Z-scores
and Mahalanobis distance. In the 3′UTR-focused analysis (last 200 nt), a marked
increase in RRACH and GGAU motif density was detected particularly in GOGAT and GS genes compared to the genomic background, showing statistically
significant deviation. Considering the motif architecture and the significant
enrichment within the 3′UTR, GOGAT
and GS genes emerge as potential
candidates in terms of m6A-related regulation. This suggests that
nitrogen metabolism genes may represent potential candidates for m6A-related
regulation within their 3′UTR regions.
Keywords: m6A methylation; 3′UTR;
RRACH motif; Nitrogen metabolism; GOGAT;
GS; Camellia sinensis.