Duanmu Deqiang, Miller Amy R, Horken Kempton M, Weeks Donald P, Spalding Martin H
Department of Genetics, Development and Cell Biology, Iowa State University, Ames, IA 50011, USA.
Proc Natl Acad Sci U S A. 2009 Apr 7;106(14):5990-5. doi: 10.1073/pnas.0812885106. Epub 2009 Mar 24.
The CO(2)-concentrating mechanism (CCM) of Chlamydomonas reinhardtii and other microalgal species is essential for photosynthetic growth in most natural settings. A great deal has been learned regarding the CCM in cyanobacteria, including identification of inorganic carbon (Ci; CO(2) and HCO(3)(-)) transporters; however, specific knowledge of analogous transporters has remained elusive in eukaryotic microalgae such as C. reinhardtii. Here we investigated whether the limiting-CO(2)-inducible, putative ABC-type transporter HLA3 might function as a HCO(3)(-) transporter by evaluating the effect of pH on growth, photosynthetic Ci affinity, and [(14)C]-Ci uptake in very low CO(2) conditions following RNA interference (RNAi) knockdown of HLA3 mRNA levels in wild-type and mutant cells. Although knockdown of HLA3 mRNA alone resulted in only modest but high-pH-dependent decreases in photosynthetic Ci affinity and Ci uptake, the combination of nearly complete knockdown of HLA3 mRNA with mutations in LCIB (which encodes limiting-Ci-inducible plastid-localized protein required for normal Ci uptake or accumulation in low-CO(2) conditions) and/or simultaneous, apparently off-target knockdown of LCIA mRNA (which encodes limiting-Ci-inducible plastid envelope protein reported to transport HCO(3)(-)) resulted in dramatic decreases in growth, Ci uptake, and photosynthetic Ci affinity, especially at pH 9, at which HCO(3)(-) is the predominant form of available Ci. Collectively, the data presented here provide compelling evidence that HLA3 is directly or indirectly involved in HCO(3)(-) transport, along with additional evidence supporting a role for LCIA in chloroplast envelope HCO(3)(-) transport and a role for LCIB in chloroplast Ci accumulation.
莱茵衣藻和其他微藻物种的二氧化碳浓缩机制(CCM)对于大多数自然环境中的光合生长至关重要。关于蓝藻中的CCM,我们已经了解了很多,包括无机碳(Ci;CO₂和HCO₃⁻)转运蛋白的鉴定;然而,在诸如莱茵衣藻这样的真核微藻中,类似转运蛋白的具体知识仍然难以捉摸。在这里,我们通过评估pH对野生型和突变体细胞中HLA3 mRNA水平经RNA干扰(RNAi)敲低后在极低CO₂条件下的生长、光合Ci亲和力和[¹⁴C]-Ci摄取的影响,来研究限制CO₂诱导的假定ABC型转运蛋白HLA3是否可能作为HCO₃⁻转运蛋白发挥作用。尽管单独敲低HLA3 mRNA仅导致光合Ci亲和力和Ci摄取有适度但高度依赖pH的降低,但HLA3 mRNA几乎完全敲低与LCIB突变(其编码在低CO₂条件下正常Ci摄取或积累所需的限制Ci诱导的质体定位蛋白)和/或同时明显脱靶敲低LCIA mRNA(其编码据报道运输HCO₃⁻的限制Ci诱导的质体包膜蛋白)的组合导致生长、Ci摄取和光合Ci亲和力急剧下降,特别是在pH 9时,此时HCO₃⁻是可用Ci的主要形式。总体而言,本文提供的数据提供了令人信服的证据,表明HLA3直接或间接参与HCO₃⁻运输,同时还有额外证据支持LCIA在叶绿体包膜HCO₃⁻运输中的作用以及LCIB在叶绿体Ci积累中的作用。