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ORF Homology
ORF Start1
ORF Stop
TATA box
Polyadenylation Signal
Homology of predicted 1° Sequence2
Notes
UL 23 (TK) 1059 73 1118 73 Herpesvirus TK Polyadenylation seq. is noncanonical (AATTAA)
UL 24 1008 1949 1053 1857 or 1895 or 50403
Herpesvirus UL24 Polyadenylation seq. is noncanonical (AATAA or AAATA); may use the polyA site adjacent to UL26;
GAGCAAT sequence4 at 1006
UL 25 1606 3279 1856 3287 or 5040 Herpesvirus UL25 Polyadenylation seq. is noncanonical (AAATAA); may use the polyA site adjacent to UL26
UL 26 3357 5006 3288 or
3305
5040 Herpesvirus assemblin, aas 30-250 of 549
TATA is noncanonical (AATAA or TTTAA)
UL26.5 4125 5006 4043, 4059, 4389,
or 4087
5040 Turtle herpesvirus UL26.5
TATA is noncanonical (TATTT or TAATAA)
Supplemental Data Table 1: Putative Transcription Signals in the FPTHV contig
UL 27
(gB)
7713 5155 7445 5261 Herpesvirus gB CCAAT sequence5 at 7608
UL 28 9962 7710 10147 7920 or 5261 Herpes processing and transport protein
Could co-utilize the polyA site adjacent to UL27
UL 29 13735 10877 13683 or
13882
10091 Herpes single-stranded DNA binding protein
TATA is noncanonical (TATTTA or AATAA); GC box6 at 13780
UL 30
(pol)
13896 17171 13686 17397 DNA polymerase B TATA is noncanonical (ATAAAA) but precedented in VZV7; CCAAT sequence2 at 12734
UL 31 18207 17284 18275 17770 Herpes UL31 TATA is noncanonical (ATTAAA); CCAAT sequence4 at 18244; GGGCGG sequence6 at 18343
UL 32 19573 18200 19891 18275 or 17770 Herpes major envelope glycoprotein
Could co-utilize the polyA site adjacent to UL31; GC
box5 at 19900
UL 33 19805 20140 19892 21415 Herpes UL33 CCAAT sequence4 at 19513; polyadenylation seq. is absent, must utilize the polyA site adjacent to UL35;
GGGCGG sequence6 at 19423
UL 34 20153 20947 19892 21415 Herpes UL34,
residues 45-220 of 264
Polyadenylation seq. is absent; must utilize the polyA site adjacent to UL35; GC box5 at 20465
UL 35 20995 21360 20943 21415 TATA is noncanonical (TTTAA)
UL 36 Beyond edge of contig
21378 Beyond edge of contig
21394 Herpes UL36
1ORF start is reported as the first ATG codon; in cases where the first TATA homology follows the first ATG it is likely that transcription initiates from an internal ATG
2Identified by RPS-BLAST
3 “Coterminal families” of herpesvirus genes may coutilize a polyadenylation signal (Draper et al., J. Virol. 57:1023; Proudfoot&Brownlee, Nature 263:211)
4CCAAT transcription initiation co-signal (Chodesh et al., Cell 53:11)
5(A/G)(A/G)GCAAT transcription initiation co-signal (reviewed by Corden et al., Science 209:1406)
6GGGCGG transcription initiation signal (McKnight et al., Cell 37:253)
7Noncanonical transcription signals in Human Herpesvirus 3 reviewed by Cohen&Straus, Fields Virology.