Table 4. List of oligodeoxyribonucleotides used in this study.
The following primers were designed to create and confirm the strains deleted for eif3h+ | |||
---|---|---|---|
Name | Nucleotide sequences (5′ to 3′) | Gene | |
1 | eIF3h-FW | TAGAAAAGGTTTAATAAAACTGGTAGG CTCCTCTATTCTATAACTTGTAATCGCC GACAGCCATGGCTTTAAAAAGTTGCCG GATCCCCGGGTTAATTAA TTAAGTAGATCCTTTTATTTTAATGCTAC GAGGTATAACTAGTGAGAGTGAAGAAGA ATGCTCCATTTTTTATAAACAAAGAATTC |
eif3h |
2 | eIF3h-RV | GAGCTCGTTTAAAC | eif3h |
3 | eIF3h-up | GAGCTTAAGGCCGAGAAAAC | eif3h |
4 | eIF3h-down | TATGCTGTATCAAGAAAACC | eif3h |
5 | ura4-midF | GTGTGTACTTTGAAAGTCTAGCTTTA | ura4 |
6 | ura4-midR | CCTTGTATAATACCCTCGCC | ura4 |
The following primers were designed by the Bähler group in their microarray studies 61 | |||
7 | 2-A11_C418.01c_his4_F | TAGAGAACTCCTTTGGCGGA | his4 |
8 | 2-A11_C418.01c_his4_R | CAACTTCGACAGCAGGATGA | his4 |
9 | 20-G9_arg3_F | TCTCCAGGCGTTAGCAGATT | arg3 |
10 | 20-G9_arg3_R | TGCATGAATTTGCAGCTAGG | arg3 |
11 | 2-E7_C1105.02c_lys4_F | CAACCGTGTTGGTATTGCTG | lys4 |
12 | 2-E7_C1105.02c_lys4_R | GCGACAAGGTTTTCAAGCTC | lys4 |
13 | 53-F9_atf1 mts1 sss1 gad7_F | ACCCCTACTGGAGCTGGATT | atf1 |
14 | 53-F9_atf1 mts1 sss1 gad7_R | TACCTGTAACAGCTTGGGGG | atf1 |
15 | 27-H10_cr1 mts2 F | CGCTTCTAAATTTCGCCAGA | pcr1 |
16 | 27-H10_cr1 mts2_R | GGTGTTGATTTGGAGGGAGA | pcr1 |
17 | 33-G9_gpd1_F | GGTGTAGTTGGCTCCGGTAA | gpd1 |
18 | 33-G9_gpd1_R | TCTCACAGAATTGCTCACGG | gpd1 |
19 | 12-F1_cta1_F | TTCGTGATCCCGCTAAATTC | cta1 |
20 | 12-F1_cta1_R | AAGGTAAAGCGTCCAACCCT | cta1 |
The following primers were designed by the group of K. Ohta (see Fig. 7C) | |||
21 | cta3 ORF-5′ | CGAACATTGGCTTCTCC | cta3 |
22 | cta3 ORF-3′ | GGTTGCGTAACAAATTCC | cta3 |
23 | cta3 CRE-5′ | TAACAACACTCCGCCATTCG | cta3 |
24 | cta3 CRE-3′ | TGACTCCGACATTGATTTCCT | cta3 |