Department of Biological Sciences, Dartmouth College, Hanover, NH 03755, USA.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22534-9. doi: 10.1073/pnas.0908718106. Epub 2009 Dec 10.
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.
在 drnl-2 背景下的基因筛选中,我们分离出 miR319a 的一个功能丧失等位基因(miR319a(129))。先前,miR319a 被推测在叶片发育中发挥作用,这是基于异位表达 miR319a(jaw-D)的植物出现明显卷曲叶片表型。miR319a(129) 突变体在花瓣和雄蕊发育中出现缺陷;花瓣狭窄且短,雄蕊在花药发育中出现缺陷。miR319a(129) 功能丧失等位基因在编码 miRNA 的中间有一个单碱基变化,这降低了 miR319a 识别靶标的能力。对 miR319 基因家族的三个成员(miR319a、miR319b 和 miR319c)的表达模式进行分析表明,这些基因的表达模式基本没有重叠,这表明这些基因具有不同的发育功能。miR319a 通过调节 TCP 转录因子 TCP2、TCP3、TCP4、TCP10 和 TCP24 发挥作用;这些 TCP 基因的 RNA 表达水平在 jaw-D 中下调,在 miR319a(129)中上调。有几条证据表明 TCP4 是 miR319a 的一个关键靶标。首先,tcp4(soj6) 突变体含有与 miR319a(129)突变互补的 TCP4 miRNA 结合位点突变,抑制 miR319a(129)的花表型。其次,在花瓣和雄蕊中表达野生型 TCP4(即 AP3:TCP4)对花发育没有影响;相比之下,当在花瓣和雄蕊中表达 miRNA 抗性版本的 TCP4(即 pAP3:mTCP4)时,这些器官不会发育。令人惊讶的是,当 AP3:TCP4 存在于 miR319a(129)背景中时,花瓣和雄蕊的发育严重受到干扰,这表明 miR319a 对 TCP4 的适当调节对这些花器官至关重要。