miR319a targeting of TCP4 is critical for petal growth and development in Arabidopsis

花瓣 雄蕊 生物 突变体 遗传学 基因 拟南芥 表型 等位基因 突变 损失函数 基因表达 小RNA 植物 花粉
作者
Anwesha Nag,Stacey King,Thomas Jack
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:106 (52): 22534-22539 被引量:460
标识
DOI:10.1073/pnas.0908718106
摘要

In a genetic screen in a drnl-2 background, we isolated a loss-of-function allele in miR319a ( miR319a 129 ). Previously, miR319a has been postulated to play a role in leaf development based on the dramatic curled-leaf phenotype of plants that ectopically express miR319a ( jaw-D ). miR319a 129 mutants exhibit defects in petal and stamen development; petals are narrow and short, and stamens exhibit defects in anther development. The miR319a 129 loss-of-function allele contains a single-base change in the middle of the encoded miRNA, which reduces the ability of miR319a to recognize targets. Analysis of the expression patterns of the three members of the miR319 gene family ( miR319a , miR319b , and miR319c ) indicates that these genes have largely non-overlapping expression patterns suggesting that these genes have distinct developmental functions. miR319a functions by regulating the TCP transcription factors TCP2 , TCP3 , TCP4 , TCP10 , and TCP24 ; the level of RNA expression of these TCP genes is down-regulated in jaw-D and elevated in miR319a 129 . Several lines of evidence demonstrate that TCP4 is a key target of miR319a . First, the tcp4 soj6 mutant, which contains a mutation in the TCP4 miRNA-binding site complementary to the miR319a 129 mutation, suppresses the flower phenotype of miR319a 129 . Second, expression of wild-type TCP4 in petals and stamens (i.e., AP3:TCP4) has no effect on flower development; by contrast, a miRNA-resistant version of TCP4 , when expressed in petals and stamens (i.e., pAP3:mTCP4) causes these organs not to develop. Surprisingly, when AP3:TCP4 is present in a miR319a 129 background, petal and stamen development is severely disrupted, suggesting that proper regulation by miR319a of TCP4 is critical in these floral organs.
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