Yamasaki Hiroaki, Hayashi Makoto, Fukazawa Mitsue, Kobayashi Yoshichika, Shikanai Toshiharu
Graduate School of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Plant Cell. 2009 Jan;21(1):347-61. doi: 10.1105/tpc.108.060137. Epub 2009 Jan 2.
Expression of miR398 is induced in response to copper deficiency and is involved in the degradation of mRNAs encoding copper/zinc superoxide dismutase in Arabidopsis thaliana. We found that SPL7 (for SQUAMOSA promoter binding protein-like7) is essential for this response of miR398. SPL7 is homologous to Copper response regulator1, the transcription factor that is required for switching between plastocyanin and cytochrome c(6) in response to copper deficiency in Chlamydomonas reinhardtii. SPL7 bound directly to GTAC motifs in the miR398 promoter in vitro, and these motifs were essential and sufficient for the response to copper deficiency in vivo. SPL7 is also required for the expression of multiple microRNAs, miR397, miR408, and miR857, involved in copper homeostasis and of genes encoding several copper transporters and a copper chaperone, indicating its central role in response to copper deficiency. Consistent with this idea, the growth of spl7 plants was severely impaired under low-copper conditions.
在拟南芥中,miR398的表达是对铜缺乏的响应而被诱导的,并且参与编码铜/锌超氧化物歧化酶的mRNA的降解。我们发现SPL7(SQUAMOSA启动子结合蛋白样7)对于miR398的这种响应至关重要。SPL7与铜响应调节因子1同源,铜响应调节因子1是莱茵衣藻中响应铜缺乏时在质体蓝素和细胞色素c6之间转换所必需的转录因子。SPL7在体外直接结合到miR398启动子中的GTAC基序,并且这些基序对于体内对铜缺乏的响应是必需且充分的。SPL7对于参与铜稳态的多个微小RNA(miR397、miR408和miR857)以及编码几种铜转运蛋白和一种铜伴侣蛋白的基因的表达也是必需的,这表明其在响应铜缺乏中起核心作用。与这一观点一致,在低铜条件下,spl7植物的生长受到严重损害。