Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Protein Sci. 2022 May;31(5):e4297. doi: 10.1002/pro.4297.
ATP-binding cassette (ABC) systems, characterized by ABC-type nucleotide-binding domains (NBDs), play crucial roles in various aspects of human physiology. Human ABCG5 and ABCG8 form a heterodimeric transporter that functions in the efflux of sterols. We used sequence similarity search, multiple sequence alignment, phylogenetic analysis, and structure comparison to study the evolutionary origin and sequence signatures of ABCG5 and ABCG8. Orthologs of ABCG5 and ABCG8, supported by phylogenetic analysis and signature residues, were identified in bilaterian animals, Filasterea, Fungi, and Amoebozoa. Such a phylogenetic distribution suggests that ABCG5 and ABCG8 could have originated in the last common ancestor of Amorphea (the unikonts), the eukaryotic group including Amoebozoa and Opisthokonta. ABCG5 and ABCG8 were missing in genomes of various lineages such as snakes, jawless vertebrates, non-vertebrate chordates, echinoderms, and basal metazoan groups. Amino-acid changes in key positions in ABCG8 Walker A motif and/or ABCG5 C-loop were observed in most tetrapod organisms, likely resulted in the loss of ATPase activity at one nucleotide-binding site. ABCG5 and ABCG8 in Ecdysozoa (such as insects) exhibit elevated evolutionary rates and accumulate various changes in their NBD functional motifs. Alignment inspection revealed several residue positions that show different amino-acid usages in ABCG5/ABCG8 compared to other ABCG subfamily proteins. These residues were mapped to the structural cores of transmembrane domains (TMDs), the NBD-TMD interface, and the interface between TMDs. They serve as sequence signatures to differentiate ABCG5/ABCG8 from other ABCG subfamily proteins, and some of them may contribute to substrate specificity of the ABCG5/ABCG8 transporter.
ATP 结合盒(ABC)系统,以 ABC 型核苷酸结合域(NBD)为特征,在人体生理学的各个方面发挥着关键作用。人类 ABCG5 和 ABCG8 形成异二聚体转运体,负责固醇的外排。我们使用序列相似性搜索、多重序列比对、系统发育分析和结构比较来研究 ABCG5 和 ABCG8 的进化起源和序列特征。通过系统发育分析和特征残基支持的 ABCG5 和 ABCG8 的直系同源物在两侧对称动物、Filasterea、真菌和变形虫中被鉴定出来。这种系统发育分布表明,ABCG5 和 ABCG8 可能起源于 Amorphea(单系生物)的最后共同祖先,包括变形虫和后生动物的真核生物组。ABCG5 和 ABCG8 在各种谱系的基因组中缺失,例如蛇、无颌脊椎动物、非脊椎脊索动物、棘皮动物和基础后生动物群。在大多数四足动物生物中,观察到 ABCG8 Walker A 基序和/或 ABCG5 C 环中关键位置的氨基酸变化,这可能导致一个核苷酸结合位点的 ATP 酶活性丧失。后生动物(如昆虫)中的 ABCG5 和 ABCG8 表现出较高的进化率,并在其 NBD 功能基序中积累了各种变化。对齐检查揭示了几个残基位置,与其他 ABCG 亚家族蛋白相比,ABCG5/ABCG8 中的这些残基位置使用不同的氨基酸。这些残基被映射到跨膜结构域(TMD)的结构核心、NBD-TMD 界面和 TMD 之间的界面。它们作为序列特征,将 ABCG5/ABCG8 与其他 ABCG 亚家族蛋白区分开来,其中一些残基可能有助于 ABCG5/ABCG8 转运体的底物特异性。