Genome-wide identification of ATP-binding cassette transporter B subfamily, focusing on its structure, evolution and rearrangement in ciliates

Author:

Zhang Xue12,Zhao Yan3ORCID,Zheng Weibo4,Nan Bei12,Fu Jinyu12,Qiao Yu12,Zufall Rebecca A.5,Gao Feng126ORCID,Yan Ying12ORCID

Affiliation:

1. Institute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong 266003, People's Republic of China

2. Key Laboratory of Evolution & Marine Biodiversity (OUC), Ministry of Education, Qingdao 266003, People's Republic of China

3. College of Life Sciences, Capital Normal University, Beijing 100048, People's Republic of China

4. School of Life Sciences, Ludong University, Yantai, Shandong 264025, People's Republic of China

5. Department of Biology and Biochemistry, University of Houston, Houston, TX 77204, USA

6. Laboratory for Marine Biology and Biotechnology, Laoshan Laboratory, Qingdao 266237, People's Republic of China

Abstract

ATP-binding cassette subfamily B (ABCB) has been implicated in various essential functions such as multidrug resistance, auxin transport and heavy metal tolerance in animals and plants. However, the functions, the genomic distribution and the evolutionary history have not been characterized systematically in lower eukaryotes. As a lineage of highly specialized unicellular eukaryotes, ciliates have extremely diverse genomic features including nuclear dimorphism. To further understand the genomic structure and evolutionary history of this gene family, we investigated the ABCB gene subfamily in 11 ciliates. The results demonstrate that there is evidence of substantial gene duplication, which has occurred by different mechanisms in different species. These gene duplicates show consistent purifying selection, suggesting functional constraint, in all but one species, where positive selection may be acting to generate novel function. We also compare the gene structures in the micronuclear and macronuclear genomes and find no gene scrambling during genome rearrangement, despite the abundance of such scrambling in two of our focal species. These results lay the foundation for future analyses of the function of these genes and the mechanisms responsible for their evolution across diverse eukaryotic lineages.

Funder

Young Taishan Scholar Program of Shandong Province

Beijing Natural Science Foundation

Laoshan Laboratory

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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