Molecular basis of essential amino acid transport from studies of insect nutrient amino acid transporters of the SLC6 family (NAT-SLC6)

被引:52
作者
Boudko, Dmitri Y. [1 ]
机构
[1] Rosalind Franklin Univ, Dept Physiol & Biophys, Chicago Med Sch, RFUMS, N Chicago, IL 60064 USA
关键词
Insect nutrition; Essential amino acids; Epithelial absorption; Transporters; Midgut; Alimentary canal; BORDER MEMBRANE-VESICLES; H+-V-ATPASE; BASOLATERAL MEMBRANES; BACTERIAL HOMOLOG; EPITHELIAL-CELLS; K+-TRANSPORT; NUTRITIONAL REQUIREMENTS; FUNCTIONAL EXPRESSION; NEURONAL EXCITABILITY; SODIUM SYMPORTER;
D O I
10.1016/j.jinsphys.2011.12.018
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Two protein families that represent major components of essential amino acid transport in insects have been identified. They are annotated as the SLC6 and SLC7 families of transporters according to phylogenetic proximity to characterized amino acid transporters (HUGO nomenclature). Members of these families have been identified as important apical and basolateral parts of transepithelial essential amino acid absorption in the metazoan alimentary canal. Synergistically, they play critical physiological roles as essential substrate providers to diverse metabolic processes, including generic protein synthesis. This review briefly clarifies the requirements for amino acid transport and a variety of amino acid transport mechanisms, including the aforementioned families. Further it focuses on the large group of Nutrient Amino acid Transporters (NATs), which comprise a recently identified subfamily of the Neurotransmitter Sodium Symporter family (NSS or SLC6). The first insect NAT, cloned from the caterpillar gut, has a broad substrate spectrum similar to mammalian B-0 transporters, Several new NAT-SLC6 members have been characterized in an effort to explore mechanisms for the essential amino acid absorption in model dipteran insects. The identification and functional characterization of new B-0-like and narrow specificity transporters of essential amino acids in fruit fly and mosquitoes leads to a fundamentally important insight: that NATs evolved and act together as the integrated active core of a transport network that mediates active alimentary absorption and systemic distribution of essential amino acids. This role of NATs is projected from the most primitive prokaryotes to the most complex metazoan organisms, and represents an interesting platform for unraveling the molecular evolution of amino acid transport and modeling amino acid transport disorders. The comparative study of NATs elucidates important adaptive differences between essential amino acid transportomes of invertebrate and vertebrate organisms, outlining a new possibility for selective targeting of essential amino acid absorption mechanisms to control medically and economically important arthropods and other invertebrate organisms. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:433 / 449
页数:17
相关论文
共 134 条
[2]   Characterization of a functional bacterial homologue of sodium-dependent neurotransmitter transporters [J].
Androutsellis-Theotokis, A ;
Goldberg, NR ;
Ueda, K ;
Beppu, T ;
Beckman, ML ;
Das, S ;
Javitch, JA ;
Rudnick, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (15) :12703-12709
[3]   Identification of two cationic amino acid transporters required for nutritional signaling during mosquito reproduction [J].
Attardo, Geoffrey M. ;
Hansen, Immo A. ;
Shiao, Shin-Hong ;
Raikhel, Alexander S. .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2006, 209 (16) :3071-3078
[4]   The SLC6/NSS family members KAAT1 and CAATCH1 have weak chloride dependence [J].
Bette, Sara ;
Castagna, Michela ;
Bossi, Elena ;
Peres, Antonio ;
Sacchi, Vellea Franca .
CHANNELS, 2008, 2 (05) :358-362
[5]   The Developmental, Molecular, and Transport Biology of Malpighian Tubules [J].
Beyenbach, Klaus W. ;
Skaer, Helen ;
Dow, Julian A. T. .
ANNUAL REVIEW OF ENTOMOLOGY, 2010, 55 :351-374
[6]   Identification of LAT4, a novel amino acid transporter with system L activity [J].
Bodoy, S ;
Martín, L ;
Zorzano, A ;
Palacín, M ;
Estévez, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (12) :12002-12011
[7]  
Böhmer C, 2005, BIOCHEM J, V389, P745
[8]   The SLC36 family: proton-coupled transporters for the absorption of selected amino acids from extracellular and intracellular proteolysis [J].
Boll, M ;
Daniel, H ;
Gasnier, B .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2004, 447 (05) :776-779
[9]   Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter [J].
Boll, M ;
Herget, M ;
Wagener, M ;
Weber, WM ;
Markovich, D ;
Biber, J ;
Clauss, W ;
Murer, H ;
Daniel, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :284-289
[10]   Oligomeric structure of the neutral amino acid transporters KAAT1 and CAATCH1 [J].
Bossi, Elena ;
Soragna, Andrea ;
Miszner, Andreea ;
Giovannardi, Stefano ;
Frangione, Valeria ;
Peres, Antonio .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2007, 292 (04) :C1379-C1387