Vrille (gene)

Interlocked molecular feedback loops in Drosophila melanogaster. CLOCK/CYCLE heterodimer acts as transcriptional activator (positive element) for period (per) and timeless (tim) genes. The heterodimer of PER/TIM is phosphorylated in the cytoplasm in the presence of specific kinases, and the phosphorylated complex then acts as inhibitor for its own transcription (negative element). The VRI and PDP1 proteins regulate the levels of CLK/CYC complex, which in turn are regulated by CLK/CYC. Thus, CLK/CYC heterodimer appears to be an important component that connects the two loops and is important for sustaining molecular oscillations. The protein Cryptochrome (CRY) has been implicated in the light entrainment pathways of the Drosophila molecular clock.

The current model of the Drosophila circadian oscillator is composed of two interlocking transcription/translation negative feedback loops. One loop consists of per, tim, clk, cyc, and their mRNA and protein products. In this loop, the PER/TIM heterodimer is a repressor for the CLK/CYC complex while the CLK/CYC complex serves as an activator and transcription factor for per and tim. Vrille is activated by the CLK/CYC complex and encodes a repressor of CLK transcription.[5][6] The second regulatory loop is composed of vri, pdp1, clk, and their mRNA and protein products. Vrille is activated by the CLK/CYC complex and encodes a repressor of CLK transcription. High levels of CLK/CYC activate the transcription of Vrille mRNA to increase protein production, leading to transcriptional repression of clk which ultimately reduces the concentration of CLK/CYC complexes.[6] Lastly, PDP1 protein, a bZIP transcription factor, serves as an activator of clk transcription and peaks 3–6 hours after the VRI protein peak and, together with VRI, regulate daily rhythms in CLK protein.[7]

Vrille acts as an enhancer of decapentaplegic (dpp) and easter, genes critical to the development of dorsal/ventral axis in the process of regional differentiation during Drosophila embryogenesis. Likewise, it can act as an enhancer of dpp mutations. Easter is involved in initiating a protease cascade that activates the dorsal gene, resulting in repression of dpp in the ventral portion of the embryo during early fly development. The mechanism by which vrille affects the dpp pathway is still unknown.[8]

mRNA analysis and bioinformatic analysis have suggested that vrille is involved in the regulatory networks leading to cardiac senescence. In addition, overexpression of vri has led to heart dysfunctions, while a loss of function significantly reduces age-related cardiac dysfunction as a result of oxidative stress reduction [9]

Induction of vri in Drosophila eye precursor cells, the underdeveloped cells that will become cells of the eye, both reduces the number of ommatidia while simultaneously altering their internal structures. Overexpression of vri causes anti-proliferative effects in processes vital for limb generation, as well as abnormal phenotypes in salivary glands and internal organs. Lastly, it has been postulated that vri affects these processes by interacting with genes involved in the production of cytoskeleton although the exact process is still unknown[10]