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Small-interfering RNAs from natural antisense transcripts derived from a cellulose synthase gene modulate cell wall biosynthesis in barley

机译:来自纤维素合酶基因的天然反义转录物的小干扰RNA调节大麦细胞壁的生物合成

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摘要

Small-interfering RNAs (siRNAs) from natural cis-antisense pairs derived from the 3′-coding region of the barley (Hordeum vulgare) CesA6 cellulose synthase gene substantially increase in abundance during leaf elongation. Strand-specific RT-PCR confirmed the presence of an antisense transcript of HvCesA6 that extends ≥1230 bp from the 3′ end of the CesA-coding sequence. The increases in abundance of the CesA6 antisense transcript and the 21-nt and 24-nt siRNAs derived from the transcript are coincident with the down-regulation of primary wall CesAs, several Csl genes, and GT8 glycosyl transferase genes, and are correlated with the reduction in rates of cellulose and (1 → 3),(1 → 4)-β-D-glucan synthesis. Virus induced gene silencing using unique target sequences derived from HvCesA genes attenuated expression not only of the HvCesA6 gene, but also of numerous nontarget Csls and the distantly related GT8 genes and reduced the incorporation of D-14C-Glc into cellulose and into mixed-linkage (1 → 3),(1 → 4)-β-D-glucans of the developing leaves. Unique target sequences for CslF and CslH conversely silenced the same genes and lowered rates of cellulose and (1 → 3),(1 → 4)-β-D-glucan synthesis. Our results indicate that the expression of individual members of the CesA/Csl superfamily and glycosyl transferases share common regulatory control points, and siRNAs from natural cis-antisense pairs derived from the CesA/Csl superfamily could function in this global regulation of cell-wall synthesis.
机译:来自大麦(大麦)CesA6纤维素合酶基因3'编码区的天然顺反义对的小干扰RNA(siRNA)在叶片伸长过程中的丰度大大提高。链特异性RT-PCR证实了HvCesA6反义转录物的存在,该反义转录物从CesA编码序列的3'末端延伸≥1230bp。 CesA6反义转录物以及源自该转录物的21-nt和24-nt siRNA的丰度增加与原壁CesAs,一些Cs1基因和GT8糖基转移酶基因的下调相吻合,并且与降低纤维素的比率,以及(1→3),(1→4)-β-D-葡聚糖的合成。使用源自HvCesA基因的独特靶序列进行病毒诱导的基因沉默,不仅减弱了HvCesA6基因的表达,而且减弱了许多非靶标Csls和远距离相关的GT8基因的表达,并减少了D- 14 C-的掺入Glc进入纤维素并进入发育叶片的混合连接(1→3),(1→4)-β-D-葡聚糖。相反,CslF和CslH的独特靶序列沉默了相同的基因,降低了纤维素和(1→3),(1→4)-β-D-葡聚糖合成的速率。我们的结果表明,CesA / Csl 超家族的单个成员和糖基转移酶的表达具有共同的调控点,而天然 cis -反义对中的siRNA来源于< em> CesA / Csl 超家族可能在这种细胞壁合成的整体调控中起作用。

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