International Journal of Genomics

Volume 2014 (2014), Article ID 402603, 9 pages

http://dx.doi.org/10.1155/2014/402603

Research Article

Molecular Evolution of the Vertebrate FK506 Binding Protein 25

Fei Liu,1,2 Xiao-Long Wei,³ Hao Li,1,2 Ji-Fu Wei,² Yong-Qing Wang,² and Xiao-Jian Gong¹

¹Department of Pharmacology, China Pharmaceutical University, Nanjing 210009, China

²Research Division of Clinical Pharmacology, The First Affiliated Hospital, Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, China

³Department of Pathology, Cancer Hospital of Shantou University Medical College, Shantou, China

Received 25 November 2013; Accepted 16 January 2014; Published 2 March 2014

Academic Editor: Huai-Rong Luo

Copyright © 2014 Fei Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

FK506 binding proteins (FKBPs) belong to immunophilins with peptidyl-prolyl isomerases (PPIases) activity. FKBP25 (also known as FKBP3) is one of the nuclear DNA-binding proteins in the FKBPs family, which plays an important role in regulating transcription and chromatin structure. The calculation of nonsynonymous and synonymous substitution rates suggested that FKBP25 undergoes purifying selection throughout the whole vertebrate evolution. Moreover, the result of site-specific tests showed that no sites were detected under positive selection. Only one PPIase domain was detected by searching FKBP25 sequences at Pfam and SMART domain databases. Mammalian FKBP25 possess exon-intron conservation, although conservation in the whole vertebrate lineage is incomplete. The result of this study suggests that the purifying selection triggers FKBP25 evolutionary history, which allows us to discover the complete role of the PPIase domain in the interaction between FKBP25 and nuclear proteins. Moreover, intron alterations during FKBP25 evolution that regulate gene splicing may be involved in the purifying selection.

1. Introduction

Immunophilins include three families with peptidyl-prolyl isomerases (PPIases) activity, FK506 binding proteins (FKBPs), cyclophilins, and parvulins. FKBPs are named for binding to the immunosuppressive drug FK506, characterized by one or more PPIase domains. The 15 identified members of human FKBPs are divided into 4 groups: cytoplasmic, TPR domain, endoplasmic reticulum (ER), and nucleus. FKBP25 and FKBP133 locate in the nucleus, containing a single PPIase domain [1].

FKBP25 (also known as FKBP3) is the first mammalian FKBP with a calculated molecular mass of 25 kDa found in the nucleus, which plays a role in regulating transcription and chromatin structure. The FKBP25 comprises a conserved PPIase domain at its C-terminus with a 43% sequence identity to FKBP12 and a helix-loop-helix (HLH) motif at its unique hydrophilic N-terminal [2, 3]. This conserved PPIase domain functions in binding to the immunosuppressive agent FK506 or rapamycin. Unlike another FKBPs, FKBP25 shows a strong affinity for binding rapamycin (Ki = 0.9 nM) over FK506 (Ki = 200 nM) [4]. The FKBP25 was reported to be associated with nuclear proteins including transcription factor Yin-Yang1 (YY1), mouse double minute 2 (MDM2), and histone deacetylases (HDACs) [5]. FKBP25 binds to YY1 at N-terminal and increases its DNA-binding activity without the involvement of the FK506/rapamycin binding domain [6]. In addition, the level and activity of the tumor suppressor protein p53 are negatively regulated by MDM2. The HLH motif of FKBP25 mediates protein-protein interaction to enhance ubiquitination and degradation of oncogene MDM2, increasing the expression of tumor suppressor p53 and its downstream effector p21 [7]. Moreover, the protein-protein interaction contributes to form HDAC complexes, which is critical for the chromatin structure [2].

In 1992, Jin et al. reported the molecule cloning of human FKBP25 and performed a homology comparison between FKBP25 and FKBP12/FKBP13 [8]. Furthermore, Mas et al. showed the molecule cloning of mouse FKBP25 and expression pattern of FKBP25 gene during cerebral cortical neurogenesis [9]. However, the relationships between nuclear functions and evolution in FKBP25 are seldom reported. In this study, we exhibit an evolutional analysis not only on selective pressure but also on intron-exon conversion among vertebrate FKBP25 genes.

2. Materials and Methods

2.1. Sequence Data Collection

All the FKBP25 gene and amino acid sequences were obtained from the ENSEMBL (http://www.ensembl.org/index.html) [10], based on orthologous and paralogous relationships. The gained FKBP25 sequences were applied as queries to search known FKBP25 genes using BLAST at the National Center for Biotechnology Information (NCBI), in order to confirm whether their best hit was an FKBP25 gene [11].

Incomplete sequences of FKBP25 genes in four species (tree shrew, horse, platypus, and turkey) were retrieved from both ENSEMBL and NCBI. After eliminating these incomplete sequences, 28 sequences were applied for this study. The 28 sequences from 23 species comprised human (ENSG00000100442), chimpanzee (ENSPTRG00000006305), gorilla (ENSGGOG00000013322), orangutan (ENSPPYG00000005778), macaque (ENSMMUG00000016512), marmoset (ENSCJAG00000015972), mouse (ENSMUSG00000020949), rat (ENSRNOG00000004629), guinea pig (ENSCPOG00000001444), rabbit1 (ENSOCUG00000007535), rabbit2 (ENSOCUG00000026892), dog1 (ENSCAFG00000014018), dog2 (ENSCAFG00000014093), dog3 (ENSCAFG00000024192), dog4 (ENSCAFG00000000578), cow (ENSBTAG00000002610), elephant1 (ENSLAFG00000003572), elephant2 (ENSLAFG00000027553), opossum (ENSMODG00000007352), chicken (ENSGALG00000012466), zebra finch (ENSTGUG00000013231), anole lizard (ENSACAG00000004080), xenopus (ENSXETG00000003052), fugu (ENSTRUG00000011887), medaka (ENSORLG00000015070), stickleback (ENSGACG00000012834), tetraodon (ENSTNIG00000010980), and zebrafish (ENSDARG00000079018).

2.2. Molecular Phylogenetic Analyses

The protein coding sequences of FKBP25 were aligned using CLUSTAL W program in MEGA 5.05. We constructed a maximum likelihood (ML) tree of FKBP25 amino acid sequences by MEGA 5.05 with the optimal model (Kimura 2-parameter model). The relative support of internal node was performed by bootstrap analyses with 1000 replications for ML reconstructions [12].

2.3. Selection Pressure Analyses

The numbers of nonsynonymous substitutions per nonsynonymous site (dN) and the numbers of synonymous substitutions per synonymous site (dS) were computed by MEGA 5.05 with the modified Nei-Gojobori method. The dN/dS <1, =1 and >1 demonstrate purifying selection, neutral selection, and positive selection, respectively [13]. The dN is the numbers of nonsynonymous substitutions per nonsynonymous site, and the dS is the numbers of synonymous substitutions per synonymous site. The transition/transversion ratio was 1.55 estimated using the ML method by MEGA 5.05 [14].

The FASTA format of FKBP25 sequences was converted to the PAML format using DAMBE software for subsequent site analyses [13]. The CODEML program implemented in the PAML 4.7 package was used to detect positive selection of individual sites. The site-specific model was exerted using likelihood ratio tests (LRT) to compare M7 (null model) with M8 model. M7 is a null model that does not allow for any codons with , whereas M8 model allows for positively selective sites (). When the M8 model fitted the data significantly (-value < 0.05) better than the null model (M7), the presence of sites with is suggested. On the contrary, the results of value > 0.05 proved the absence of sites with . The twice log likelihood difference between the two compared models () is compared against with critical values 5.99 and 9.21 at 0.05 and 0.01 significance levels, respectively [15].

2.4. Protein Domain and Motif Analyses

Protein domain analyses of FKBP25 were shown at Pfam domains database (http://pfam.sanger.ac.uk) [16]. SMART (http://smart.embl-heidelberg.de/) was used to make sure the presence of FKBP25 domains [17]. The motifs of FKBP25 were analyzed by the MEME software (http://meme.sdsc.edu/meme/website/intro.html) with a maximum of 10 motifs to find [18].

2.5. Exon-Intron Conservation Analyses

We collected elaborate information about FKBP25 exon and intron from ENSEMBL (http://www.ensembl.org/index.html) [19]. The number and length of FKBP25 exon and intron in 28 sequences were investigated for exon-intron conservation analyses.

3. Results

3.1. Phylogenetic Analyses of FKBP25

All the FKBP25 gene and protein sequences were collected from the ENSEMBL and checked by BLAST at NCBI. The sequence and structural alignment of FKBP25 was shown in Figure 1. The phylogenetic tree was constructed according to the protein coding sequences of FKBP25 using the maximum likelihood method (Figure 2, left panel). The FKBP25 genes from the primate lineage and teleost lineage form a species-specific cluster, respectively. Four FKBP25 isoforms of dog exhibited a close relationship and clustered together, according to the phylogenetic tree. There were similar phenomena in rabbit and elephant.

Figure 1: Sequence and structural alignment of FKBP25.

Figure 2: Phylogenetic tree and motif distributions of FKBP25.

3.2. Selection Pressure Analyses

The nonsynonymous to synonymous rate ratio (dN/dS) may demonstrate the selective pressures of involved protein. We calculated the pairwise distance of FKBP25 sequences using MEGA 5.05. There was a significantly lower dN than dS in the pairwise comparisons of these sequences. Most values of dN/dS in these sequences were distributed blow the diagonal, showing that the presence of a purifying selection existed in the FKBP25 (Figure 3). The comparisons of average dN and dS in various vertebrate groups were shown in Figure 4, respectively. Furthermore, site-specific tests were performed for searching the positive selection sites in vertebrate, mammalian, primate, and mammalian excluding primate, rodent and teleost lineages. Although some positive selection sites were computed, each of M7 and M8 <5.99 indicated that the M8 model was not significantly better than the M7 model to fit the data. Consequently, we concluded that the site-specific analyses also compute no positive selection sites acting on FKBP25 using PAML4.7 (Table 1).

Table 1: Site-specific tests for positive selectionof FKBP25.

Species
Models
Estimates of parameters
lnL

Positively selected sites

Vertebrate
M7

−5463.938465
0.003806
NA

M8

−5463.940368
None

()  

Mammalian
M7

−2182.244789
0.000258
NA

M8

−2182.244918
None

        ()  

Primate
M7

−997.077389
0.000102
NA

M8

−997.077440
None

        ()  

Mammalian excluding primate
M7

−2242.306222
0.000160
NA

M8

−2242.306302
NS

        ()  

Rodent
M7

−1372.902164
0.000058
NA

M8

−1372.902193
NS

        ()  

Teleost
M7

−2354.923181
0.000408
NA

M8

−2354.923385
NS

()  

lnL: the log-likelihood difference between the two models; : twice the log-likelihood difference between the two models (In all the species, , the -value is more than the significance level 0.05, indicating that M8 model is not better than M7 model); NA: not allowed; NS: not shown (it means the sites under positive selection but not reaching the significance level of 0.9).

Figure 3: Pairwise comparisons of dN and dS among 28 vertebrate FKBP25 sequences.

Figure 4: The average nonsynonymous (dN) and synonymous (dS) in FKBP25 from different vertebrate groups. The value of average dN was in blue, and the value of average dS was in red.

3.3. Protein Domain and Motif Analyses

Early studies reported that mammalian FKBP25 have two portions: one is a putative helix-loop-helix motif within N-terminal unique sequence (Figure 5(a)) and the other is the PPIase domain at its C-terminus (Figure 5(b)) [20].

(a)

(b)

Figure 5: Sequence logos (MEME LOGOs) of conserved motifs identified in vertebrate FKBP25.

The domain distribution of FKBP25 was investigated using FKBP25 to search amino acid sequences at the Pfam database firstly. Only one domain (PPIase domain) was found in the Pfam database. The PPIase domain within FKBP25 sequences generally started at position 122 and ended at position 221. Similarly, we further make sure that the FKBP25 domain is at SMART, resulting in the single PPIase domain at position 119 to 221.

We then performed a detailed domain and motif analyses using the MEME software. Except two dog isoforms, dog2 and dog3, the FKBP25 sequences used in this study contain a conversed PPIase domain within motif 1 (shown in Figure 2) at its C-terminus. In addition, the result implied that motif 2 located in the N-terminal contained an HLH motif [6], which was associated with DNA binding and dimerization [21]. However, HLH motif was not found in dog3, anole lizard, and teleost lineage, implying that these FKBP25 proteins may function on gene expression in another pathway.

3.4. Exon-Intron Conservation Analyses

The exon-intron information collected from the ENSEMBL database was shown in Table 2 and Figure 6. Most of the FKBP25 genes have 7 exons with similar length in different species (Table 2). Mammalian FKBP25 shows exon-intron conservation with 6 introns and similar sizes of each intron. Intron deletions existed in several isoforms of species. The rabbit2 isoform had 2 exons, and elephant2 isoform had only one exon. The exon numbers of dog2, dog3, and dog4 isoforms were less than seven. Except mammalian FKBP25 genes, anole lizard reduced one exon compared with mammalian and birds, but the xenopus and teleost maintained 7 exons. The intron deletions of FKBP25 genes may happen in the evolutionary process from amphibian to reptile. Then, a subsequent intron insertion occurred in the evolution from reptile to more advanced animals. The FKBP25 genes also had intron insertion in zebra finch and zebra fish.

Table 2: Exon and intron lengths of FKBP25.

Species
Length (bp)

Exon1
Intron1
Exon2
Intron2
Exon3
Intron3
Exon4
Intron4
Exon5
Intron5
Exon6
Intron6
Exon7
Intron7
Exon8
Total exons

Human
108
3548
102
797
108
8173
136
530
68
2761
98
1775
55
—
—
675

Chimpanzee
108
3524
102
797
108
8898
136
530
68
2725
98
1789
55
—
—
675

Gorilla
108
3538
102
796
108
8214
136
530
68
2753
98
1778
55
—
—
675

Orangutan
108
3498
102
793
108
8395
136
533
68
2457
98
1432
55
—
—
675

Macaque
108
3496
102
786
108
8273
136
531
68
2845
98
1818
55
—
—
675

Marmoset
108
3592
102
780
108
5644
136
507
68
2537
98
2100
55
—
—
675

Mouse
108
3762
102
841
108
2224
136
837
68
1961
98
937
55
—
—
675

Rat
108
3528
102
816
108
2030
136
942
68
1667
98
1118
55
—
—
675

Guinea pig
108
3232
102
772
108
3600
136
1416
68
1346
98
1340
55
—
—
675

Rabbit1
108
2189
102
1082
108
4634
136
1115
68
1826
98
1266
55
—
—
675

Rabbit2
620
40
55
—
—
—
—
—
—
—
—
—
—
—
—
675

Dog1
108
2573
102
1076
108
2088
136
468
68
1823
98
1216
55
—
—
675

Dog2
296
13
229
4
129
—
—
—
—
—
—
—
—
—
—
654

Dog3
30
2
195
4
252
2
33
2
33
12
102
—
—
—
—
645

Dog4
427
190
248
—
—
—
—
—
—
—
—
—
—
—
—
675

Cow
108
2332
102
603
108
2835
136
484
68
1706
98
1309
55
—
—
675

Elephant1
108
3176
102
1089
108
4756
136
483
68
1580
98
1725
55
—
—
675

Elephant2
675
—
—
—
—
—
—
—
—
—
—
—
—
—
—
675

Opossum
108
2560
102
1484
108
2807
136
1051
68
1261
98
554
55
—
—
675

Chicken
111
76
102
75
114
408
136
1040
68
1011
98
829
55
—
—
684

Zebra finch
111
112
102
76
108
494
136
892
97
2054
16
69
53
49
55
678

Anole lizard
186
1699
108
1333
136
1078
68
824
98
610
55
—
—
—
—
651

Xenopus
111
2319
102
403
108
418
136
129
68
186
98
787
55
—
—
678

Fugu
105
375
102
78
105
65
136
82
68
68
98
106
55
—
—
669

Medaka
105
109
102
71
99
738
136
75
68
70
98
804
55
—
—
663

Stickleback
105
294
102
76
102
93
136
135
68
81
98
96
55
—
—
666

Tetraodon
105
305
102
80
102
75
136
91
68
70
98
75
55
—
—
666

Zebra fish
105
2527
102
447
16
1117
20
244
16
359
19
904
28
108
11
666

Intron8
Exon9
Intron9
Exon10
Intron10
Exon11
Intron11
Exon12
Intron12
Exon13
Intron13
Exon14
Intron14
Exon15
Intron15

1042
24
316
26
708
14
99
10
98
31
107
15
26
76
1784

Exon16
Intron16
Exon17

98
118
55

(a) Mammalian

(b) Chicken

(c) Zebra finch

(d) Anole lizard

(e) Xenopus

(f) Teleost excluding zebrafish

(g) Zebrafish

(h) Rabbit2

(i) Elephant2

(j) Dog2

(k) Dog3

(l) Dog4

Figure 6: Exon-intron conservation among FKBP25 genes.

4. Discussion

FKBP25 is a nuclear member of the FKBPs family that is associated with transcription and chromatin structure [2]. The interactions of FKBP25 with nuclear proteins are closely associated with HLH motif at the N-terminal of FKBP25. However, whether the PPIase domain at C-terminus is important for these interactions remains uncertain. The selection pressure analyses revealed that the purifying selection triggered a whole evolutionary history of FKBP25 in vertebrates, even in each lineage of vertebrates. Purifying selection is one of the natural selections that resist deleterious mutations with negative selective coefficients [22]. The mutations that disrupt the correct folding of the FKBP25 domain can weaken PPIase activity and may be the deleterious mutations [5]. It was hypothesized that the mutations of PPIase domain were one of explanations behind the purifying selection throughout FKBP25 evolution. Therefore, although the PPIase domain of FKBP25 was not found to be involved in the protein interactions previously, the PPIase domain might have some associations with the YY1 DNA-binding, MDM2 autoubiquitination and degradation, and HDACs complex formation. These inferences will become a potent direction for exploring the relationship between nuclear proteins and PPIase domain in the future.

The protein-coding sequence length of vertebrate FKBP25 is highly conversed that almost all the taxa are 224 bp; nevertheless the original gene length and exon-intron status are tremendously various among vertebrate species. However, mammalian FKBP25 exhibit exon-intron conservation with 6 introns and similar sizes of each intron. Chicken FKBP25 maintains 6 introns, but zebra finch has one more intron that inserts in the gene. Similarly, a large variability of intron number and sizes among all the taxa shown in Figure 6 revealed that intron insertion and deletion events happened frequently during the FKBP25 evolutionary history from teleost to birds. In particular, zebrafish demonstrated the maximum number of introns in this study, and the size of exon is much smaller than other teleost species (Figure 6(g)). The intron loss of FKBP25 gene from species more advanced than zebrafish is likely to induce alterations of gene expression due to the absence of specific intron splicing. Under the purifying selection, the FKBP25 gene expression event continuously removes the pernicious mutations that may associate with intron splicing regulation [23].

FKBP25 gene knockdown declined the expression levels of p53 and p21, which emphasized the significance of FKBP25 in regulating p53 and subsequently p21 expression through controlling the ubiquitination of MDM2. Both the FKBP25 PPIase domain and its N-terminal portion were critical for the ubiquitination and degradation of MDM2 [2]. Moreover, Jin et al. reported that FKBP25 prefers to bind to rapamycin rather than FK506, implying that FKBP25 may be an important target molecule for immunosuppression by rapamycin [8]. All the evolution analyses indicated the conservation of FKBP25 gene in vertebrates. Therefore, FKBP25 possesses some basic functions in vertebrate species, like regulating p53 and p21 expression and binding to rapamycin for immunosuppression, reinforcing the suggestion that the purifying selection triggered the evolution of vertebrate FKBP25.

In conclusion, FKBP25 as a nuclear FKBP subjects to the purifying selection throughout the whole evolution, which implied the complete role of the PPIase domain involved in the interaction between FKBP25 and the nuclear proteins that are needed to be discovered continually. Additionally, incomplete exon-intron conservation of FKBP25 meets the vertebrate lineage. The intron gain or loss among the taxa is likely to be involved in the purifying selection.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Fei Liu and Xiao-Long Wei contributed to this paper equally.

Acknowledgments

This project was sponsored by the Grants from the National Natural Science Foundation of China (81273593, 81273274, and 81302331), the Priority Academic Program Development of Jiangsu Higher Education Institutions, National Major Scientific, Technological Special Project for “Significant New Drugs Development” (2011ZX09302-003-02), Jiangsu Province Major Scientific and Technological Special Project (BM2011017), Jiangsu Province’s Key Provincial Talents Program (RC201170 and H201108), and the Foundation of the Nanjing Pharmaceutical Association, China (Nanjing, China) (Grant no. H2011YX001).

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