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Tài liệu Báo cáo khoa học: Four divergent Arabidopsis ethylene-responsive element-binding factor domains bind to a target DNA motif with a universal CG step core recognition and different flanking bases preference pptx

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Tiêu đề Four divergent Arabidopsis ethylene-responsive element-binding factor domains bind to a target DNA motif with a universal CG step core recognition and different flanking bases preference
Tác giả Shuo Yang, Shichen Wang, Xiangguo Liu, Ying Yu, Lin Yue, Xiaoping Wang, Dongyun Hao
Trường học Jilin University
Chuyên ngành Plant molecular biology
Thể loại Journal article
Năm xuất bản 2009
Thành phố Changchun
Định dạng
Số trang 10
Dung lượng 3,33 MB

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Nội dung

In vitro and in vivo binding assays of the four AtERFs with the DRE motif showed that the recognition of the CG step was indispensable in all four of the specific binding reactions, imply

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element-binding factor domains bind to a target DNA

motif with a universal CG step core recognition and

different flanking bases preference

Shuo Yang1, Shichen Wang1, Xiangguo Liu1, Ying Yu1, Lin Yue3, Xiaoping Wang1

and Dongyun Hao1,2

1 Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education, Jilin University, Changchun, China

2 Biotechnology Research Centre, Jilin Academy of Agricultural Sciences (JAAS), Changchun, China

3 School of Physical Education, Northeast Normal University, Changchun, China

Introduction

The ethylene-responsive element-binding factor (ERF)

gene family of transcriptional factors is one of the

largest transcriptional factor gene families in the plant

kingdom [1,2] The ERF domain was first identified as

a conserved motif of 58–59 amino acids in four

DNA-binding proteins from tobacco and was shown to bind specifically to a GCC box [3] After the completion of the sequencing of the Arabidopsis genome [4], 124 genes were predicted to encode proteins belonging to the AtERF family [2]

Keywords

CG step; DRE motif; ERF domain;

homology; universal binding characteristic

Correspondence

D Hao, Biotechnology Research Centre,

Jilin Academy of Agricultural Sciences

(JAAS), Changchun 130033, China

Fax: +86 431 87063080

Tel: +86 431 87063195

E-mail: dyhao@cjaas.com

(Received 31 August 2009, revised

29 September 2009, accepted 8 October

2009)

doi:10.1111/j.1742-4658.2009.07428.x

The Arabidopsis ethylene-responsive element-binding factor (AtERF) fam-ily of transcription factors has  120 members, all of which possess a highly conserved ERF domain AtERF1, AtERF4, AtEBP and CBF1 are members from different phylogenetic subgroups within the family Electrophoretic mobility shift assay analyses revealed that the ERF domains of these four proteins were capable of binding specifically to either GCC or dehydration-responsive element (DRE) motifs In vitro and in vivo binding assays of the four AtERFs with the DRE motif showed that the recognition of the CG step was indispensable in all four

of the specific binding reactions, implying that there may be a universal binding characteristic of various ERF domains binding to a given con-sensus (e.g the DRE motif) In addition, the core DNA-binding motifs preferred by the four AtERFs were identified, and all of these motifs contained a conserved CG step core Thus, conserved recognition of the

CG step may be the foundation of the formation of the stable complex

by the ERF domain with the DRE motif, which is probably determined

by the highly conserved residues presented in the DNA contact surface among the whole AtERF family members The different preferences at flanking bases of individual ERF domains, which appear to be attrib-uted to the subfamily- or subgroup-specific residues, may be essential discrimination of the target binding motif from various similar sequences

by divergent AtERF domains

Abbreviations

DBD, DNA binding domain; DRE, dehydration-responsive element; EMSA, electrophoretic mobility shift assay; ERE, ethylene-responsive element; ERF, ethylene-responsive element-binding factor.

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The AtERF family is further divided into various

subgroups according to the homology of ERF

domains [5,6]

An ERF domain consists of a three-stranded

anti-parallel b-sheet and an a-helix, packed approximately

parallel to the b-sheet, with the seven thoroughly

con-served amino acids (Arg6, Arg8, Trp10, Glu16, Arg18,

Arg26 and Trp28) in the b-sheet contacting uniquely

with the bases of the target DNA at the major groove

(see Fig 1A) [7] Phylogenetic analyses of the ERF

domains of all members within the AtERF family

show that the residues Arg6, Glu16 and Trp28 are

completely conserved among all 124 members, whereas

more than 95% of members contain the Arg8, Arg18, Arg26 residues [6]

From the results of the few AtERFs studied, however, the conserved ERF domains do not seem to prefer identical DNA consensus sequences For ins-tance, some AtERFs have been shown to bind in vitro

to the ethylene-responsive element (ERE), a GCCGCC motif designated the GCC motif [3,8–12], to conduct GCC motif-mediated transcription (activation or repres-sion) in leaves of Arabidopsis [12] This ERE was first reported to be a binding site (referred to as the GCC box) of a number of tobacco ERF proteins [3] and it was later presumed to be the target site of many other ERF proteins [2]

The ERF protein, AtEBP, was also found to protect the GCC box in a DNase I foot-printing analysis [10]

In contrast, the dehydration-responsive element (DRE), with the TACCGACAT motif, in the drought-responsive gene rd29A from Arabidopsis has been proven to be the recognition site of DRE-binding proteins, which are transcription factors that have authentic ERF domains [13] and that are involved in the induction of rd29A expression by low-temperature stress A similar element to DRE, the C-repeat (TGGCCGAC) has been identified in the cold-induc-ible gene cor15a and it is reported to function in cold-response regulation through binding by another ERF protein, CBF1 [14]

The similarity of these ERF-binding elements and the high similarity of ERF domains among the mem-bers of the entire ERF family have led to speculation that the ERF domains from various subgroups within the AtERF family recognize a certain binding site with universal binding characteristic to a conserved core The divergent short flanking bases, on the other hand, allow preference to govern differential recognition We have previously demonstrated that various ERF domains had divergences in their DNA recognition modes [9], but, to date, additional supporting evidence has been lacking Indeed, little is still known regarding the ways in which these differences are important for the functionalities of members in the AtERF family, the majority of which have not yet been studied

In the present study, we selected four representatives from different functional subgroups of the AtERF family and characterized the in vivo and in vitro bind-ing specificities of the four ERF domains for a sequence containing the DRE motif In addition, we used a random sequence selection method to identify the core recognition motifs preferred by each of the four domains A universal binding characteristic was revealed, in addition to the individual features of vari-ous ERF domains involved in recognition of the DRE

A

B

C

Fig 1 (A) Solution structure of AtERF1–GCC box complex (PDB

code: 1GCC) [7] The DNA-binding domain is shown in the

sche-matic; DNA is represented by tubes The b-sheet of the ERF

domain is light blue and the seven conserved amino acid residues

reported to contact DNA bases directly are red; other conserved

amino acid residues that do not directly contact with DNA bases

are blue (B) The DNA base sequence with position numbering

along the 16 bp fragment of DREwt The bases in the core

ACC-GAC are in bold and boxed in gray (C) Sequence alignment of four

ERF domains of AtERF1, AtERF4, AtEBP and CBF1 The secondary

structure scheme is indicated above the sequence The conserved

amino acid residues that directly contact with DNA bases and the

other conserved amino acid residues that do not directly contact

with DNA bases are in red and blue, respectively.

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motif The results have important implications for

understanding the foundations of recognition of a

given binding site by divergent members of the AtERF

family

Results and Discussion

The members of the ERF family in Arabidopsis can be

classified into a number of different phylogentic

sub-groups according to the sequence similarity of the

ERF domains [6] We selected four AtERFs –

AtERF1, AtERF4, AtEBP and CBF1 – as

representa-tives from divergent subgroups (for details, see Figs 1C

and 6), to investigate whether the highly homologous

ERF domains of different AtERFs have universal

binding characteristics for the recognition of a given

consensus sequence (e.g DRE)

Binding specificity of AtERFs to the GCC and DRE

motifs

Having established that CBF1 can specifically

recog-nize both GCC and DRE motifs [9], the two most

popularly reported ERF-binding sites, we continued to

explore the DNA-binding specificity of the other three

AtERFs Table 1 shows that all four ERF domains

were capable of binding specifically to the 16 bp

frag-ment containing either the GCC or the DRE motif

The equilibrium dissociation constants (Kd) of

AtERF1, AtERF4 and AtEBP for binding to the DRE

motif were within the level of typical monomeric

interaction, although the binding activities were in

gen-eral lower than those for binding to the GCC motif

CBF1 appeared to bind to the DRE motif more

strongly than to the GCC motif, implying CBF1 may

prefer the DRE motif over the GCC motif To further

confirm if these variations in binding affinity were

caused by binding instability as a result of nonspecific

interference, rather than the alternation of a binding

site, we carried out the competition binding assay using a nonspecific competitor poly[dA-dT].poly[dA-dT] in an electrophoretic mobility shift assay (EMSA) Figure 2 shows that most of the AtERFs exhibited similar stability in binding to either the GCC or the DRE motif The most remarkable feature arising from the competition binding assay was the consistency of the binding preference of the AtERFs with the EMSA analysis The three AtERFs, AtERF1 AtERF4 and AtEBP, with higher sequence similarity to each other than to CBF1, had similar binding preferences in comparison with CBF1

Verification of the binding characteristics of the selected AtERFs with the DRE motif

To verify the detailed binding characteristics of the four different AtERFs to a given consensus sequence DRE, EMSAs were carried out with the DRE motif and its mutants possessing single T substitutions (see Fig 3) Each base in the DRE motif from T5 to C11 was replaced with a T, except that T5 was replaced by

A, and the binding free energy changes (DDG) were obtained from quantitative titration analysis Figure 3 shows that AtERF1 and AtERF4 exhibited the highest specific interactions at C7, C8, G9 or C11, because the

Table 1 Binding activities of the selected AtERFs to GCC and

DRE motif-containing sequences Four ERF domains were tested

for binding to the 16 bp DRE or GCC motif-containing sequences

using quantitative EMSA, as described in Materials and methods.

K d values are represented as the mean of three replicates ±

stan-dard deviation The Kdvalue for nonspecific binding was estimated

to be  1 l M or higher.

Fig 2 Competition binding assay of the ERF–DNA complex The binding complex of the ERFs and their binding DNAs were incu-bated together with 0, 0.001, 0.01, 0.1, 1.0 and 10 lg poly[dA-dT].poly[dA-dT] in a 10 lL volume and analysed by EMSA, as described in the Materials and methods.

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base substitution at that position caused the greatest

decline in binding activity AtEBP requested C8, G9

and C11 most frequently and with the moderate

requirements of C7 As for CBF1, the prerequisite

bases appeared to be C8 and G9, whereas the other bases within the binding motif were only moderately required to varying extents In the four reactions, bases C8 and G9 in the DRE motif were absolutely requested by all AtERFs for specific binding, indicat-ing that the recognition of the CG step was conserved

by various AtERFs and may be the universal binding characteristic of different AtERFs in recognition with the DRE motif In addition, bases C7 and C11 within the motif were required to different extents by AtERFs from the divergent phylogentic subgroups, implying that the recognition of these bases was the individual feature of distinct AtERFs binding to the DRE motif

In vivo DNA binding specificity of AtERFs by the reporter–effector transient assay

To confirm if these binding specificities of AtERFs observed in vitro were also capable of regulating the DRE-mediated transcription within plant tissue, repor-ter effect cotransformation assays were carried out An effector plasmid possessing the coding region of the full-length AtERF1, AtEBP or CBF1 genes driven by the CaMV 35S promoter, together with the luciferase reporter gene containing four tandem copies of either the DRE motif or its mutants at the upstream regula-tory region, was coexpressed into Arabidopsis leaves by particle bombardment Figure 4 shows that these three AtERFs were able to transactivate the transcription of

a gene carrying the wild-type DRE motif (DREwt), which was represented by an increase in luciferase activity of about four- to seven-fold over the control

No luciferase activity was detected when any of the three ERF effectors was cotransformed with a reporter carrying DREt1, in which the C8 was replaced by

T Although AtERF1 did not activate transcription of the reporter gene carrying either DREt2 or DREt3, the coexpressions of AtEBP and CBF1 activated tran-scription of DREt3 reporter genes to varying degrees

As AtERF4 was a repressor, an extra effector in which the activation domain of viral protein 16 was fused to the yeast GAL4 DNA binding domain (DBD) and then coexpressed with the AtERF4 effector was used

to test the in vivo binding specificity of AtERF4 The reporter gene containing multicopies of the GAL4 binding sequence was inserted into the existing lucifer-ase reporter next to the four tandem DRE motifs and the transcription suppression by AtERF4 was assayed Figure 5 shows that AtERF4 suppressed viral protein

16 activation by more than 50% when cotransformed with the reporter carrying DREwt, whereas no repres-sion was detected with a reporter having mutant DRE motifs in which C8, G9 or C11 were replaced by T

0

1

2

3

4

5

0

1

2

3

4

5

0

1

2

3

4

5

0

1

2

3

4

5

AtERF1

AtERF4

AtEBP

CBF1

–1 )

–1 )

Fig 3 Effect of single base substitutions on the relative binding

free energy change (DDG) in the binding of the four ERF domains

to the DRE motif The DNA sequence shown at the bottom is the

DRE motif in which each base was substituted individually one by

one as illustrated The solid bars indicate the increase in DDG

caused by the base substitution at the corresponding position

Posi-tive DDG represents a decreased binding activity; a 10-fold

decrease in binding activity increased DDG by  1.3 kcalÆmol)1.

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These observations were consistent with the findings in

the in vitro single base substitution binding assays: the

substitution at C8 or G9 abolished the specific

recogni-tion of the DRE motif by all four of the AtERFs

Random binding site selection reveals the

binding characteristics of divergent AtERFs

to the DRE motif

To clarify the possible existence of the moderately

divergent binding motifs of the four AtERFs from the

divergent phylogenetic subgroups, randomized

oligonu-cleotide selection was performed The resulting binding motif of hexamers selected by these four ERF domains

is shown in Table 2 AtERF1 seemed to prefer the hexamer GCCGCC motif, which is consistent with the results from previous studies [7,8] Although the AtERF4 required a relatively relaxed G or A at posi-tion 2 of the hexamer G⁄ aCCGCC, AtEBP selected a binding motif of hexamer GCCGCC The selected motif of CBF1, AA⁄ cCGAC, appears to agree with a previous report [14] Although each ERF domain showed different binding preferences, all of the binding sites selected by the AtERFs from the four subgroups possessed a common CG core in the centre and a con-served C at the last position (position 7) These moder-ately divergent bases existed in the other positions within the binding motifs, discriminating the members from different subgroups

The solution structure of the complex formed by the ERF domain of AtERF1 with the GCC box (1GCC) shows that two categories of residues within the domain are considered to be important for specific DNA bind-ing: one consists of the residues in the b-sheet directly contacting the DNA bases; and the other is made up of the numerous Ala residues in the a-helix and the hydro-phobic residues with larger side chains in the b-sheet (in particular Phe13, Phe32, Val27 and Ile17), which appears to determine the geometry of the a-helix rela-tive to the b-sheet [3–5,7–9,17] A multiple alignment of Arabidopsis ERF domains (Fig 6) shows that a series

of residues (e.g Gly4, Arg6, Arg8, Gly11, Glu16, Ile17, Arg18, Arg26, Trp28, Leu29, Gly30, Ala38, Ala39, Asp43 and Asn57) were almost absolutely conserved among all members of the ERF family Most of these residues are present in the b-sheet, especially Arg6, Arg8, Glu16, Arg18, Arg26 and Trp28 (Fig 1A), which are reported to contact directly with DNA, suggesting that the conformation of a partial DNA contact surface may be conserved among various ERF domains, which result in the conserved recognition of the CG step in the DRE motif by all four of the different AtERFs

On the other hand, some other residues reported to determine the geometry of the a-helix relative to the b-sheet were not as conserved as these other residues, but instead were subfamily or subgroup specific, e.g the Ile17 in almost all of the ERF family (V17 in CBF1), V27 in ERF subfamily (Ile27 or Leu27 in the DRE-binding protein subfamily) and Tyr42 in the major ERF family (His42 in the CBF1 and TINY sub-group) (Fig 6) However, these subfamily- or group-specific residues seem not to be involved in the direct base contact, which may affect the local conformation

of the interface by the determination of the geometry

of the a-helix relative to the b-sheet It seems that the

Reporters

Effectors

4 x DRE

Ω

0

2

4

6

8

10

DREwt

0

2

4

6

8

10

DREt2

DREt1

DREt3 Binding motifs:

l

o

t

n

o

C

1

F

B

1

F

R

t

A

P

B

t

A

l

o

t

n

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C

1

F

B

1

F

R

t

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P

B

t

A

Fig 4 AtERF1, AtEBP and CBF1 activate the transcription of the

luciferase reporter gene driven by the DRE motif and its mutants.

The luciferase reporter gene contains four copies of the cis-acting

binding motif, DREwt, DREt1, DREt2 or DREt3, which are

high-lighted and underlined The effector was constructed with a full

length of ERF cDNA that was controlled under the CaMV 35S

pro-moter following a translation enhancer (X) from tobacco mosaic

virus These effectors induce transactivation of the reporter gene.

The control in the transient assay was the same as the

experi-ments without the addition of an effector The results are shown

as relative luciferase activity per control.

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flanking positions, as well as the CG step core in the

DNA motif, were required to varying extents by

diver-gent ERF domains, and may be determined by these

subfamily- or group-specific residues

The biological function in DNA binding of

individ-ual ERF domains is apparently determined by the

primary structures of the divergent DBD and a

phylo-genetic classification of the ERF family may partly

reflect the features in DNA binding of a certain

popu-lation of ERF domains The observations acquired in

the present study imply that the divergent ERF

domains from various groups of the family bind to a

given consensus sequence by conserved recognition of

a CG step core as the universal binding characteristic

This may be the foundation of the formation of a sta-ble ERF–DNA complex and the different flanking position preferences by individual ERF domains may

be crucial for the precise regulation of their own target genes by various ERFs

Materials and methods

Preparation of ERF domain-containing proteins The coding region of the ERF domain of CBF1 (Uni-ProtKB: P93835) (amino acids 47–142), which contains 10 and 38 amino acids in the N- and C-terminal regions, respectively, was prepared as described previously [9] The

Fig 5 AtERF4 suppresses the transcription of the luciferase

repor-ter gene driven by the DRE motif and it mutants A multicopy of

the GAL4 binding sequence was inserted into the DRE:luciferase

reporter next to the 4· DRE motif An extra effector was

con-structed carrying the coding sequences of the activation domain of

viral protein 16 and the yeast GAL4 DBD The reporter and two

effectors in a ratio of 1 : 1 : 1 were cotransformed into plant tissue;

the remainder was the same as in Fig 4.

Table 2 Selection of binding sites from a random oligonucleotide pool by ERFs Selections were performed using a 60 bp oligonu-cleotide containing a randomized site of 10 bp The selected sequences were aligned computationally and the appearance of a base at each position in a motif was presented as a percentage fre-quency of all four kinds of base The base with a frefre-quency higher than 50% (bold) was defined as the selected site If the second highest frequency base showed not less than half the highest fre-quency (marked with an asterisk), it was defined as the second possible site and is presented in lower case letter.

Proteins

Selection position

Frequency (%)

Deduced consensus

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Fig 6 Sequence alignment of ERF domains of members of the Arabidopsis ERF family All ERF domain sequences were aligned and classi-fied according to the results from the phylogenetic tree The names of the ERF domains are represented by their gene locus numbers except that the names of the four domains used in this study are represented by the transcriptional factor names The secondary structure indicated above the sequence and the seven conserved amino acid residues reported to contact DNA bases directly [7] are in red; other conserved amino acid residues that do not directly contact DNA bases are in blue.

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ERF domains of AtERF1 (UniProtKB: O80337), AtERF4

(UniProtKB: O80340) and AtEBP (UniProtKB: P42736)

with 10 and 8 amino acids in the terminal regions,

respec-tively, were prepared according to the previous work of Hao

pET16b plasmid (Novagen, Merck, Darmstadt, Germany)

Fig 6 (Continued ).

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and the corresponding proteins were expressed in

BL21(DE3) pLysS (Merck) Escherichia coli cells and

puri-fied using a His-Trap his-tagged protein purification kit

(Amersham Pharmacia Biotech, Uppsala, Sweden) The

pro-tein concentrations were determined using the bicinchoninic

acid protein assay kit (Pierce, Chester, UK) and further

confirmed using the method of Gill and von Hippel [18]

EMSA

Two 16 bp fragments, EREwt (5¢-CATAAGAGCCGCC

ACT-3¢) and DREwt (5¢-ATACTACCGACATGAG-3¢)

(for DNA base sequence and position numbering of

DREwt, see Fig 1B), from the promoter region of the

tobacco Gln2 gene [3] and the Arabidopsis rd29A gene [19],

respectively, were prepared, together with their mutants, by

synthesizing both stands The EMSA, binding titration

analysis and the calculation of the binding free energy

change (DDG) were performed as described previously [8,9]

Binding competition assay

The binding condition and buffers used in the competition

assay were the same as used in the quantitative

DNA-bind-ing assay described above The radioisotope-labelled DNA

probe was first mixed with the binding protein at a

concen-tration corresponding to its Kd After allowing it to

com-plex for 5 min at room temperature, the mixture was

distributed into aliquots, to which a

poly.[d(A-T)].poly[dA-dT] (Amersham Pharmacia Biotech) gradient of 0.001–

10 lg was added to a final volume of 10 lL of each

aliquot After incubation for a further 10 min, the contents

were loaded on to an 8% nondenaturing PAGE and

visual-ized as for EMSA

Construction of the reporter and effector genes

For the reporter gene constructs, see Fig 4 The detailed

dual-luciferase reporter transient assay was performed as

described previously [9]

Selection of the DNA-binding site

A 60 bp single-stranded DNA RDM10, with 10

random-ized oligonucleotides in the center, i.e CTGTCAGTGAT

CTTAGC was synthesized A 100 ng sample of RDM10

was radiolabelled during synthesis of double-stranded DNA

(New England Biolabs, Ipswich, MA, USA) The selections

were performed after incubation with the individual ERF

domains (25–100 ng) followed by EMSA Briefly, each

binding reaction was carried out in a 10 lL binding buffer

[25 mm Hepes-KOH (pH 7.5), 40 mm KCl, 0.1 mm EDTA,

poly(dI–dC)] and 25–100 ng of individual ERF domain The bound oligonucleotides were gel purified, extracted with phenol⁄ chloroform and precipitated with ethanol The puri-fied DNAs were radiolabelled during amplification by PCR using 5¢ and 3¢ primers in the presence of [32

P]dATP[aP] This product was used for the next round of selection follow-ing the same protocol After seven cycles of selection, the retarded DNA band of the final selection was cut off, puri-fied and then cloned into the pUC119 plasmid (New England

insert-containing colonies were prepared and the insert fragments were sequenced At least 25 of the resulting quality sequences containing the randomized 10 bp oligonucleotides were aligned computationally using clustal x [20] The frequency

of each nucleotide appearing in the aligned position of the selected sequences was calculated, leading to the establish-ment of the selected binding site

Phylogenetic analysis The amino acid sequences of all AtERFs were downloaded from the Database of Arabidopsis Transcription Factors (DATF) (http://datf.cbi.pku.edu.cn) [21] The sequences of all ERF domains were extracted in bulk by a manual pro-gram using Perl script The sequence alignment was gener-ated using clustal x: Gap at 10; Gap Extension at 0.2; Delay Divergent Sequence at 10%; Negative Matrix Off and Protein Weight Matrix of BLOSUM Series [20]

Acknowledgements

The experiments were carried out at the National Insti-tute of Advanced Industrial Science and Technology, Japan DH was a recipient of a fellowship from the former Agency of Industrial Science and Technology, MITI, Japan, and of an STA fellowship from the Science and Technology Agency of Japan This study was also supported partially by a grant issued by the National Natural Science Foundation of China (grant

no 30470159⁄ C01020304) and the National High-Technology Research and Development Program (‘863’ Program) of China (grant no 2007AA10Z110)

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