Open Access

Evolutionary divergence and functions of the human acyl-CoA thioesterase gene (ACOT) family

Human Genomics20104:411

https://doi.org/10.1186/1479-7364-4-6-411

Received: 25 July 2010

Accepted: 25 July 2010

Published: 1 August 2010

Abstract

The acyl-CoA thioesterase gene (ACOT) family encodes enzymes that catalyse the hydrolysis of acyl-CoA thioester compounds, also known as activated fatty acids, to their corresponding non-esterified (free) fatty acid and coenzyme A (CoASH). These enzymes play a very important role in lipid metabolism by maintaining cellular levels and proper ratios of free and activated fatty acids, as well as CoASH. Within the acyl-CoA family there are two distinct subgroups, type I and type II. Despite catalysing the same reaction, the two groups are not structurally similar and do not share sequence homology, strongly suggesting convergent evolution. This suggestion is further supported if one compares the human with the mouse and rat ACOT gene families. To date, four human type I ACOTs have been identified which belong to the α/β-hydrolase fold enzyme superfamily. Type II ACOTs fall into the 'hot dog' fold superfamily. There are currently six human type II genes; however, two homologous proteins, thioesterase superfamily members 4 (THEM4) and 5 (THEM5) share common type II structural features and, in the case of THEM4, acyl-CoA thioesterase activity -- suggesting that the family may be larger than previously realised. Although recent studies have greatly expanded the current understanding of these proteins and their physiological importance, there are a number of members whose functions are relatively unexplored and which warrant further investigation.

Keywords

ACOT acyl-CoA thioesterase hydrolase gene family evolution human genome

Introduction

Acyl-CoA thioesterases (ACOTs) represent a group of enzymes that metabolise acyl-CoA esters to their corresponding non-esterified fatty acid and coenzyme A (CoASH). In addition to 'acyl-CoA thioesterases', these enzymes also have been described as 'acyl-CoA hydrolases', 'acyl-CoA thioester hydrolases' and 'deacylases'. The reaction catalysed by ACOT enzymes is very important during fatty acid metabolism. As such, ACOT genes are found throughout prokaryotic and eukaryotic organisms. In mammals, acyl-CoA thioesterase expression is widespread and activity is detectable within many tissues and cell types. ACOT activity helps to regulate cellular pools, as well as proper ratios, of activated fatty acyl-CoAs (acyl-CoA esters), free fatty acids (non-esterified fatty acids) and CoASH.

These enzymes are found within a number of subcellular locations, including peroxisomes, mitochondria and the cytosol. Peroxisomal and mitochondrial ACOTs are thought to play a major role in fatty acid degradation via β-oxidation, which provides energy through the citric acid cycle, as well as in ketone body formation. In order for a fatty acid to be transported into the peroxisome for β-oxidation, it must first be activated to its coenzyme A ester by acyl-CoA synthetases. Some acyl-CoA esters undergo β-oxidation much more slowly than others -- which can effectively sequester large amounts of CoASH and limit the activity of acyl-CoA synthetases and the rate of subsequent fatty acid β-oxidation. Under these conditions, ACOTs may act to increase the levels of free CoASH, thereby restoring fatty acid β-oxidation [1]. Mammalian ACOTs are capable of metabolising a wide variety of compounds, including short-, medium- and long-chain acyl-CoAs. They can also metabolise polyunsaturated fatty acyl-CoAs, branched-chain acyl-CoAs and aromatic-acyl-CoAs [2]. These compounds are not only utilised during β-oxidation and fatty acid degradation, but also have roles in inflammation, ion channel opening, signal transduction, lipid biosynthesis and gene regulation [2, 3].

Ten human ACOT genes have been identified to date, compared with 13 in mice and 12 in rats. These genes can be divided into two groups, based upon differences in sequence and structure. The first group includes type I ACOT proteins. These enzymes are members of the α/β-hydrolase fold enzyme superfamily, which includes other esterase-activity-exhibiting enzymes such as carboxylesterases and lipases.

Type II ACOTs make up the second group; these enzymes are members of the 'hot dog' fold enzyme superfamily, which includes a wide variety of functionally diverse proteins. Despite catalysing the same reaction, type I and type II enzymes share no similarity in terms of structure or sequence -- indicating that the two groups are analogous and not homologous. This observation is reminiscent of the cytochrome P450 (CYP) and nitric oxide synthase (NOS) gene families. Studies with purified NOS proteins revealed that they possess P450-like activity; however, detailed alignment analyses showed < 15 per cent amino acid identity, thereby confirming that these two gene families were not evolutionarily related [4]. It was thus concluded that this was an example of convergent evolution. In other words, during the evolution of enzyme activities needed at a particular subcellular location (probably more than 1 billion years ago) Mother Nature needed a 'P450-like activity' and assigned that task to the nearest protein, which happened to be an NOS. The same thing most likely happened to the type I versus type II ACOTs.

The revised nomenclature for human, mouse and rat acyl-CoA thioesterase genes was established by Hunt et al. and has been accepted by the HUGO Gene Nomenclature Committee [5]. In recent years, a number of human ACOTs have been recombinantly expressed and enzymatically characterised, although the exact physiological function and importance of many of these enzymes remain unknown.

Human ACOTgenes and evolution

To date, a total of ten genes have been identified within the human genome, all of which exhibit acyl-CoA thioesterase activity (Table 1). These ten genes can be sub-divided into two distinct groups, type I and type II, based on sequence and structural homology. Type I ACOTs comprise the smaller group, which contains only four genes: ACOT1, ACOT2, ACOT4 and ACOT6. The larger group includes six genes, and these members are referred to as type II. There is no sequence homology between the two groups, and the translated proteins have very different domain architecture, indicating two distinct, evolutionarily unrelated, origins (Figure 1) and, most likely, an example of convergent evolution.
Table 1

List of all human (ACOT) with full gene name, aliases, chromosomal location, isoforms, NCBI RefSeq mRNA accession number, NCBI RefSeq protein accession number and total amino acid number (AA#)

Gene

Full gene name

Aliases

Chromosome

Isoforms

Ref mRNA

Ref protein

AA#

ACOT1

Acyl-CoA

thioesterase 1

ACH2,

CTE-1,

LACH2

14q24.3

 

NM001037161.1

NP001032238

421

ACOT2

Acyl-CoA

thioesterase 2

MTE1, PTE2,

CTE1A,

PTE2A,

ZAP128

14q24.3

 

NM006821.4

NP006812.3

483

ACOT4

Acyl-CoA

thioesterase 4

FLJ31235,

PTE-Ib,

PTE1B,

PTE2B

14q24.3

 

NM152331.3

NP689544.3

421

ACOT6

Acyl-CoA

thioesterase 6

C14orf42,

c14_5530,

MGC161656,

MGC161658

14q24.3

 

NM001037162.1

NP001032239.1

207

ACOT7

Acyl-CoA

thioesterase 7

BACH,

ACH1, ACT,

CTE-II,

LACH,

LACH1,

MGC1126

1p36.31-p36.11

hBACHa

NM007274.3

NP009205.3

370

    

hBACHb

NM181864.2

NP863654.1

380

    

hBACHc

NM181865.2

NP863655.1

350

    

hBACHd

NM181866.2

NP863656.1

329

ACOT8

Acyl-CoA

thioesterase 8

hTE, PTE1,

PTE2, PTE-2,

HNAACTE,

hACTE-III

20q13.12

 

NM005469.2

NP005460.2

319

ACOT9

Acyl-CoA

thioesterase 9

CGI-16,

MT-ACT48,

ACATE2

Xp22.11

Isoform a

NM001037171.1

NP001032248.1

448

    

Isoform b

NM001033583.2

NP001028755.2

439

ACOT11

Acyl-CoA

thioesterase 11

BFIT, THEA,

BFIT1, BFIT2,

THEM1,

STARD14,

KIAA0707

1p32.3

BFIT1

NM015547.2

NP056362.1

607

    

BFIT2

NM147161.2

NP671517.1

594

ACOT12

Acyl-CoA

thioesterase 12

Cach,

THEAL,

CACH-1,

STARD15,

MGC105114

5q14.1

 

NM130767.2

NP570123.1

555

ACOT13

Acyl-CoA

thioesterase 13

THEM2,

HT012,

MGC4961,

PNAS-27

6p22.3

Isoform 1

NM018473.3

NP060943.1

140

    

Isoform 2

NM018473.3

NP060943.1

117

THEM4

Thioesterase superfamily member 4

CTMP,

MGC29636

1q21

 

NM053055.3

NP444283.2

240

THEM5

Thioesterase superfamily member 5

FLJ37964;

MGC126659;

MGC138444

1q21.3

 

NM182578.3

NP872384.1

247

Figure 1

Domain organisation of human type I and type II acyl-CoA thioesterases (ACOTs). Closest homologues (BAAT, THEM4 and THEM5) are included for comparison. Abbreviations: ACTH, acyl-CoA thioester hydrolase domain; BAAT, bile acid CoA:amino acid N-acyltransferase; EL, esterase-lipase domain; HD, 'hot dog' fold domain; START, steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domain; THEM, thioesterase superfamily member.

The type I proteins, ACOT1, ACOT2, ACOT4 and ACOT6, share a high degree of sequence homology (Table 2). ACOT1 and ACOT2 are the most closely related, having 98 per cent amino acid sequence identity. ACOT4 is 70 per cent identical to both ACOT1 and ACOT2. ACOT6 is the least homologous, but still shares 54-57 per cent sequence identity with the other members. None of these proteins shares any significant sequence homology with the type II proteins. The four type I genes form an 80 kilobase gene cluster on chromosome 14q24.3, indicating that they most likely have arisen as the result of gene duplication.
Table 2

Amino acid sequence identity between type I and type II human acyl-CoA thioesterases (ACOTs).

Type I ACOTs

        
 

ACOT1

ACOT2

ACOT4

ACOT6

BAAT

   

ACOT1

        

ACOT2

98%

       

ACOT4

70%

70%

      

ACOT6

57%

57%

54%

     

BAAT

45%

45%

45%

37%

    

Type II ACOTs

        
 

ACOT7

ACOT8

ACOT9

ACOT11

ACOT12

ACOT13

THEM4

THEM5

ACOT7

        

ACOT8

--

       

ACOT9

19%

--

      

ACOT11

22%

--

--

     

ACOT12

24%

--

22%

51%

    

ACOT13

--

--

--

--

--

   

THEM4

--

--

--

--

--

22%

  

THEM5

--

--

--

--

--

--

37%

 

Identity was determined using BLASTP and non-redundant human protein sequences. The predominant isoform sequences were used for ACOTs having multiple protein variants. Homology was considered not significant and left blank if the observed identity was less than 15 per cent

Abbreviations: BAAT, bile acid CoA:amino acid N-acyltransferase; THEM, thioesterase superfamily member

A similar situation is observed within the mouse and rat orthologues Acot1, Acot2, Acot3, Acot4, Acot5 and Acot6, which are clustered on chromosomes 12 D3 and 6q31, respectively. A cladogram depicting the evolutionary relationships observed between human, mouse and rat type I proteins is shown in Figure 2A. This cladogram clearly shows that, prior to the mammalian radiation approximately 75 million years ago (MYA), there was a single ancestral ACOT1 (or -2) gene; after the mammalian radiation but before the mouse-rat split at approximately 15 MYA, this single ancestor divided twice to become four rodent Acot functional genes (now named Acot1, Acot3, Acot4 and Acot5). By contrast, after the mammalian radiation, the human single ancestor duplicated into a second functioning gene, leading to ACOT1 and ACOT2. On the other hand, ACOT4 and ACOT6 existed before the mammalian radiation and remain conserved to this day in human, mouse and rat.
Figure 2

Acyl-CoA thioesterase (ACOT) type I and type II cladograms. Cladograms depicting the evolutionary relationships between human, mouse (m) and rat (r) orthologous protein sequences for type I (A) and type II (B) ACOTs. Phylogenetic trees were created using ClustalW2. Human carboxylesterase 1 (CES1) is an unrelated esterase that was added simply to 'ground' the tree.

In the mouse, the ACOT3, ACOT4 and ACOT5 enzymes each exhibit specific expression patterns and enzyme substrate specificity. Human ACOT4 carries out the reactions catalysed by all three of these mouse enzymes. The lack of a human orthologue to mouse Acot3 and Acot5 was suggested to be the result of convergent evolution; it was hypothesised that convergent, functional evolution led to a reduced need for multiple enzymes in humans [6]. The Protein Basic Local Alignment Search Tool (BLASTP) analysis of all non-redundant protein sequences, however, failed to identify orthologues for ACOT3 or ACOT5 in non-rodent species. This finding suggests that ACOT4 was an ancestral gene encoding an ACOT4 enzyme with broad substrate recognition, and that gene duplication events led to ACOT1 (or -2), and that further duplication events led to the mouse Acot3 and Acot5 genes, encoding the ACOT3 and ACOT5 enzymes, which have similar substrate specificity to that of mouse ACOT4 and human ACOT4.

Differences exist among the human, mouse and rat ACOT6 orthologues. Analysis of the genomic ACOT6 sequence indicates transcription of a complete mRNA containing three exons; however, a full-length mRNA is not detectable [6]. A shorter transcript, in which the first exon was omitted, was identified. Subsequent translation begins at a methionine located within the second exon, producing a truncated protein that lacks the N-terminal acyl-CoA thioester hydrolase domain found within other type I proteins. The truncated protein contains all residues required for catalysis and could therefore still produce an active acyl-CoA thioesterase. This is not true for the mouse or rat ACOT.

The BLAST results indicate that bile acid CoA:amino acid N-acyltransferase (BAAT) is the only enzyme to share significant sequence homology with type I ACOTs. BAAT shares 45 per cent sequence identity with ACOT1, ACOT2 and ACOT4. ACOT6 shares 37 per cent sequence identity with BAAT. BAAT is known to participate in the transfer of bile acids from the acyl-CoA thioester to either glycine or taurine, which are used for bile salt secretion. BAAT contains the same domain architecture and ACOT1, ACOT2 and ACOT4; however, the catalytic triad found within the esterase-lipase domain contains a cysteine, instead of the highly conserved serine residue. This substitution may explain the difference in activity (ie transferase versus hydrolase) observed between the two enzymes. Despite sharing catalytic domains, other α/β-hydrolase fold enzyme superfamily esterases, such as carboxylesterase 1 (CES1) and acetylcholinesterase (ACHE), share very little sequence homology with their acyl-CoA thioesterase relatives. CES1 has thus been added as an evolutionarily unrelated gene to Figure 2A simply to 'ground' the dendrogram.

Type II ACOTs are strikingly less related than type I proteins. None of the type II proteins shares more than 25 per cent identity and many do not share any significant sequence similarity (Table 2). Unlike the type I genes, type II ACOTs are widely distributed throughout the genome. With the exception of ACOT13, all type II proteins contain double 'hot dog' domains, which may have evolved as a gene duplication event that allowed for the accommodation of bulky substrates [7]. ACOT7 shares 19 per cent identity with ACOT9, 22 per cent with ACOT11 and 24 per cent identity with ACOT12. ACOT9 shares 22 per cent identity with ACOT12 but displays no homology with ACOT11. ACOT8 has no significant sequence homology with any of the other type II proteins. ACOT11 and ACOT12 share 51 per cent sequence identity and both enzymes contain a C-terminal steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domain, which seems to be specific to mammalian evolution [7].

The human genome contains 15 START-containing proteins, including ACOT11 and ACOT12 [8]. The N-terminal region of both ACOTs is unrelated to any of the other START-containing enzymes, suggesting that these proteins may be the result of a gene fusion event between an acyl-thioesterase and START domain-containing sequences. Like ACOT8, ACOT13 shares no significant sequence similarity to the other type II proteins. BLAST results did identify 22 per cent sequence identity with thioesterase superfamily member 4 (THEM4 is the official name) -- also known as Akt C-terminal modulator protein (CTMP). This small degree of homology suggests that the two proteins may share common evolutionary ties. Another protein, thioesterase superfamily member 5 (THEM5) shares more than 37 per cent identity with THEM4 but lacks significant sequence homology with ACOT13. Similar to ACOT13, both THEM4 and THEM5 contain a single 'hot dog' domain. Furthermore, type II proteins, THEM4 and THEM5 do not share sequence homology with other 'hot dog' domain superfamily members. The 'hot dog' fold-containing proteins possess highly conserved structural elements that are created by highly divergent sequences [9]. This high degree of divergence makes evolutionary comparisons difficult without three-dimensional structures, because conservation of structural interactions is not directly associated with residue conservation.

BLAST results indicate that mammalian type II ACOTs are evolutionarily conserved. A cladogram depicting the evolutionary relationships observed between human, mouse and rat type II protein is shown in Figure 2B. The mouse genome contains an additional type II ACOT, Acot10, which shares approximately 95 per cent mRNA nucleotide identity with ACOT9 [10]. Unlike ACOT3 and ACOT5, however, which are found in both mouse and rat, ACOT10 has only been identified in mice, indicating that the gene duplication event occurred less than 17 MYA -- that is, after the mouse-rat split. In mouse, Acot9 is located at chromosomal location X F3 and Acot10 is found on 15 A2. The amplification and movement of genes to a new chromosomal location is often facilitated by transposable elements, as opposed to duplications occurring within close proximity on a chromosome, which are attributed to errors during meiosis [11]. The remaining seven type II ACOT genes are highly conserved among human, mouse and rat, confirming that these genes were all present in the ancestor prior to the mammalian radiation.

Type I and type II acyl-CoA thioesterases represent two structurally distinct enzyme groups. These groups catalyse the same reaction but have distinct evolutionary origins and reaction mechanisms. An unrooted dendrogram -- created using protein sequences from both type I and type II enzymes, closest-related homologues (BAAT, THEM4 and THEM5), distant α/β-hydrolase fold homologues (CES1, ACHE) and β-actin (ACTB) as an unrelated sequence -- exemplifies how dissimilar the two groups are from one another (Figure 3). It also illustrates how the type II proteins must have originated from a common, evolutionarily distant, predecessor (as reflected in individual branch proximity to the origin of the tree).
Figure 3

Unrooted dendrogram of human acyl-CoA thioesterases (ACOTs). Phylogenetic tree created using ClustalW2 and edited using TreeIllustrator. ACHE and CES1 were included as distant homologues belonging to the α/β-hydrolase fold superfamily. Bile acid acetyl Co-A:amino acid N-acyltransferase (BAAT), thioesterase superfamily members 4 and 5 (THEM4 and THEM5) are the closest-related homologues to type I (BAAT) and type II sequences (THEM4 and THEM5). ACTB was included as an unrelated sequence used to ground the tree. Type I ACOT branches are highlighted in blue, whereas type II are in red. Abbreviations: ACHE, acetylcholinesterase; ACTB; β-actin; CES1, carboxylesterase 1

Type I ACOT structures

Type I ACOTs share a high degree of sequence and structural homology. ACOT1, ACOT2 and ACOT4 contain an N-terminal acyl-CoA thioester hydrolase domain (Pfam 04775). This domain does not participate directly in catalysis, but studies indicate that the N-terminus plays an important role in regulating enzyme activity [3]. All type I proteins also contain a C-terminus esterase-lipase superfamily domain. All residues required for catalysis are located within this domain, which is also known as the α/β-hydrolase fold.

Proteins that share this common structural element make up the functionally diverse α/β-hydrolase fold superfamily of enzymes. Within this family are a number of other distantly related proteins that exhibit esterase activity, including carboxylesterases, ACHE and lipases. The superfamily has diverged greatly and many members share very little sequence homology but are considered evolutionarily linked, based on structural homology. The enzyme activity is dependent on a catalytic triad composed of highly conserved serine, histidine and aspartate residues found within the active site [12]. These three residues are conserved throughout type I ACOTs.

The crystalline structure for ACOT2 indicates that the enzyme is most likely biologically active as a monomer [13]. The structure also reveals that the N-terminal acyl-CoA thioester hydrolase domain is connected to the active site by a long loop; it is postulated that this contributes substrate specificity, although this has yet to be verified experimentally [3]. The four human type I ACOT genes are located on chromosome 14q24.3. ACOT1, ACOT2 and ACOT3 each encode a transcript containing three exons. Genomic analysis suggests that ACOT6 should encode a similar 3 exon transcript; however, the only detectable transcript is truncated and utilises a start codon located within the 3' end of exon two, resulting in the synthesis of a truncated protein [6]. In addition to the four protein-coding genes, there is one intronless pseudogene, referred to as ACOT4P, located on chromosome 19q13.12. ACOTP4 is most likely the result of retroviral action that has inserted this DNA segment elsewhere in the genome. Attempts to translate the pseudogene results in numerous in-frame stop codons.

ACOT1, ACOT2 and ACOT4 have distinct subcellular localisation patterns and substrate specificity. ACOT1 is cytosolic and primarily responsible for the metabolism of long-chain acyl-CoAs [1, 14]. ACOT2 and ACOT1 can metabolise a similar range of substrates; however, ACOT2 contains an N-terminal mitochondrial targeting signal which directs its transport to mitochondria [6]. ACOT4 contains a C-terminal peroxisomal targeting signal, directing transport to peroxisomes, where it exhibits high activity against succinyl-CoA, as well as a wide variety of short-chain dicarboxylic-CoAs. ACOT4 can also metabolise medium- and long-chain saturated- and unsaturated-CoAs [6, 15]. As previously mentioned, ACOT6 lacks the N-terminal acyl-CoA thioester hydrolase domain.

Although studies have yet to confirm the enzymatic activity of ACOT6, the fact that it contains a complete C-terminal esterase-lipase domain supports its role as a functional esterase [13]. ACOT6 is predicted to be cytosolic, due to a missense mutation which alters the peroxisomal targeting signal that is found in the Acot6 mouse ortholog [6]. The subcellular localisation and substrate specificity for each enzyme suggest that each plays an important, non-redundant function within the cell.

Type II ACOT structures

The type II enzymes are more distantly related than type II ACOTs, as indicated by the relatively low degree of sequence conservation observed between proteins. Despite the low degree of sequence homology, the enzymes are structurally related and capable of metabolising similar substrates. ACOT7, formerly called brain acyl-CoA hydrolase (BACH), has been extensively characterised, owing to recent studies that indicate arachidonoyl-CoA as a preferred substrate. The metabolism of arachidonoyl-CoA by ACOT7 gives rise to arachidonic acid and coenzyme A. Arachidonic acid serves as a precursor for a number of compounds associated with inflammation, including prostaglandins, leukotrienes and thromboxanes [16, 17]. ACOT7 also efficiently metabolises a number of long-chain-acyl-CoAs [18]. ACOT8 is found in peroxisomes, where it metabolises a diverse range of acyl-CoA compounds [1]. Substrates include short-, medium- and long-chain acyl-CoAs. ACOT8 also has high activity towards branched- and methyl-branched chain acyl-CoAs.

ACOT9 contains a mitochondrial-targeting signal and metabolises medium- to long-chain acyl-CoAs. ACOT9 exhibits the highest activity towards myristoyl-CoA, which can then be used by N-myristoyltransferase to modify proteins posttranslationally [10]. Expression of mouse ACOT11, formerly referred to as brown fat-inducible thioesterase (BFIT), increases after cold shock. This protein was found to play a role in regulating thermogenesis, which helps to maintain body temperature [19]. The human homologue, ACOT11, may be a risk factor for obesity [19]. As previously mentioned, ACOT11 and ACOT12 contain a C-terminal START domain. The START domain in animals is commonly found within homeodomain transcription factors, where lipid-binding regulates transcription [20]. The binding of lipids to the START domain in ACOT11 or ACOT12 acts as a mechanism for regulating activity and for allowing for rapid enzyme activation. The kinetic properties of ACOT11 have yet to be determined. ACOT12 has highest activity towards acetyl-CoA [21].

ACOT13, previously called thioesterase superfamily member 2 (THEM2), differs from the other type II ACOTs, in that it contains a single 'hot dog' domain. Immunocytochemistry identified ACOT13 within the cytosol and nucleus [22]. Another study indicated that the enzyme is mitochondrial [23]. The crystal structure and substrate specificity were recently determined using recombinant protein; results indicate that ACOT13 prefers medium- to long-chain-acyl-CoA thioesters [24]. Interestingly, ACOT13 interacts with a START domain-containing protein named StarD2. The addition of StarD2 decreases the Kcat of ACOT13 for a number of substrates [25]. This finding suggests that the START domains, identified in ACOT11 and ACOT12, could have a similar effect on enzyme activity. BLAST results indicate > 22 per cent sequence identity between ACOT13 and THEM4.

Two separate studies have revealed that THEM4 is a mitochondrial protein [26, 27]. Recent in vitro kinetic activity studies revealed that THEM4 is a broad-range, high-activity acyl-CoA thioesterase [28]. Similar to ACOT13, THEM4 preferentially metabolises medium- to long-chain acyl-CoA thioesters. As such, we recommend that the enzyme be renamed ACOT14 according to the accepted nomenclature established by Hunt et al. [5]. Acyl-CoA thioesterase activity has not been verified for THEM5; however, activity is probably based on the high degree of sequence identity with THEM4, but the exact role that this protein might play in fatty acid metabolism has yet to be determined.

Conclusions

The human acyl-CoA gene family represents a diverse group of enzymes that catalyse the hydrolysis of acyl-CoA thioesters to their corresponding free fatty acids and coenzyme A. These enzymes are involved in a number of cellular processes but are primarily thought to play an important role in lipid metabolism. Despite catalysing the same enzymatic reaction, the acyl-CoA thioesterase family members can be divided into two distinct groups, type I and type II. The two groups do not share common structural elements or sequence homology and are therefore considered analogous, rather than homologous, enzymes; this is probably another example of convergent evolution.

Type I proteins belong to the α/β-hydrolase fold superfamily, whereas type II proteins fall into the 'hot dog' fold superfamily. To date, four type I and six type II genes have been identified within the human genome. There are two additional genes, THEM4 and THEM5, which gene products share both structural and sequence homology with other type II proteins. THEM4 was identified as having acyl-CoA thioesterase activity and should be considered as a new family member. In the future, perhaps THEM5 should also be considered as a type II ACOT family member. Recent studies have greatly expanded the current understanding of acyl-CoA thioesterases; however, many precise physiological functions are not completely understood and warrant further investigation.

Declarations

Acknowledgements

We would like to thank our colleagues for valuable discussion and critically reviewing this manuscript. This work was supported, in part, by the following NIH grants; R01EY17963 and R21AA017754 (V.V.) and P30ES06096 (D.W.N.).

Authors’ Affiliations

(1)
Molecular Toxicology and Environmental Health Sciences Program, Department of Pharmaceutical Sciences, University of Colorado Denver
(2)
Department of Environmental Health and Center for Environmental Genetics (CEG), University of Cincinnati Medical Center

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© Henry Stewart Publications 2010