Yokoyama Shozo, Tada Takashi, Liu Yang, Faggionato Davide, Altun Ahmet
Department of Biology, Emory University, Atlanta, GA, 30322, USA.
Department of Physics, Fatih University, Istanbul, 34500, Turkey.
BMC Evol Biol. 2016 Mar 22;16:64. doi: 10.1186/s12862-016-0637-9.
Many vertebrate species use ultraviolet (UV) reception for such basic behaviors as foraging and mating, but many others switched to violet reception and improved their visual resolution. The respective phenotypes are regulated by the short wavelength-sensitive (SWS1) pigments that absorb light maximally (λmax) at ~360 and 395-440 nm. Because of strong epistatic interactions, the biological significance of the extensive mutagenesis results on the molecular basis of spectral tuning in SWS1 pigments and the mechanisms of their phenotypic adaptations remains uncertain.
The magnitudes of the λmax-shifts caused by mutations in a present-day SWS1 pigment and by the corresponding forward mutations in its ancestral pigment are often dramatically different. To resolve these mutagenesis results, the A/B ratio, in which A and B are the areas formed by amino acids at sites 90, 113 and 118 and by those at sites 86, 90 and 118 and 295, respectively, becomes indispensable. Then, all critical mutations that generated the λmax of a SWS1 pigment can be identified by establishing that 1) the difference between the λmax of the ancestral pigment with these mutations and that of the present-day pigment is small (3 ~ 5 nm, depending on the entire λmax-shift) and 2) the difference between the corresponding A/B ratios is < 0.002.
Molecular adaptation has been studied mostly by using comparative sequence analyses. These statistical results provide biological hypotheses and need to be tested using experimental means. This is an opportune time to explore the currently available and new genetic systems and test these statistical hypotheses. Evaluating the λmaxs and A/B ratios of mutagenized present-day and their ancestral pigments, we now have a method to identify all critical mutations that are responsible for phenotypic adaptation of SWS1 pigments. The result also explains spectral tuning of the same pigments, a central unanswered question in phototransduction.
许多脊椎动物利用紫外线(UV)接收来进行诸如觅食和交配等基本行为,但其他许多物种则转向了紫光接收并提高了视觉分辨率。各自的表型由短波长敏感(SWS1)色素调节,这些色素在约360纳米和395 - 440纳米处吸收光的能力最强(最大吸收波长λmax)。由于强烈的上位相互作用,关于SWS1色素光谱调谐分子基础的广泛诱变结果及其表型适应机制的生物学意义仍不确定。
由当今一种SWS1色素中的突变及其祖先色素中的相应正向突变引起的λmax位移幅度往往有显著差异。为了解决这些诱变结果,A/B比值变得不可或缺,其中A和B分别是由位点90、113和118处的氨基酸以及由位点86、90、118和295处的氨基酸形成的区域。然后,通过确定以下两点,可以识别出产生SWS1色素λmax的所有关键突变:1)具有这些突变的祖先色素的λmax与当今色素的λmax之间的差异较小(3至5纳米,取决于整个λmax位移);2)相应的A/B比值之间的差异小于0.002。
分子适应大多通过比较序列分析进行研究。这些统计结果提供了生物学假设,需要通过实验手段进行检验。现在是探索当前可用的和新的遗传系统并检验这些统计假设的恰当时机。通过评估诱变后的当今色素及其祖先色素中的λmax和A/B比值,我们现在有一种方法来识别所有负责SWS1色素表型适应的关键突变。该结果还解释了相同色素的光谱调谐,这是光转导中一个核心的未解决问题。