Table 4.
Chromosomal distribution of Ty5 insertions in Δsir strains
| Strain
|
Chr. no.
|
Coordinate
|
Locationa
|
Nearby chromosomal features
|
|---|---|---|---|---|
| Δsir2 | ||||
| T3 | I | ∼600 | T | within YAL069W, ∼153 bases from X repeat ACS |
| T4 | VII | 287 | T | 446 bases from ACS in X repeat |
| T17 | IX or X | ∼8424 | T | ∼695 bases from ACS in X repeat |
| T10 | III | 293099 | T | within HMR, 506 bases from ACS in HMR-I |
| T8 | XIV | ∼1000 | NT | within Y‘, 6165 bases from core X repeat |
| T28 | XII | 455677 | R | between genes for 5.8S and 18S rRNA |
| T4 | VI | 1511923 | D | between PAD1 and YDR539W |
| T18 | XI | 67821 | D | between MNN4 and YKT9 |
| T12 | XIV | 91046 | D | within YNL288W |
| T20 | XV | 891622 | D | between YOR306C and SLY41 |
| Δsir3 | ||||
| H29 | III | 1568 | T | within Ty5-1 (YCLWTy5-1), 515 bases from ACS in X repeat |
| H11 | IX or X | 87 | NT | within Y‘, 7632 bases from ACS in X repeat |
| H36 | IX or X | ∼97 | NT | within Y‘, ∼7622 bases from ACS in X repeat |
| H25 | IX or X | 395 | NT | within Y‘, 7324 bases from ACS in X repeat |
| H24 | I | 124455 | D | between FUN31 and TPD3 |
| H31 | IV | 131105 | D | within YDL183C |
| H1 | IV | 1186012 | D | between TRP4 and YDR355C |
| H12 | V | 260751 | D | between YER053C and GIP2 |
| H6 | XV | 721754 | D | between PET56 and HIS3 |
| H5 | XVI | 105640 | D | between TFP3 and YPL233W |
| H4 | XVI | 396718 | D | within SEN54 |
| Δsir4 | ||||
| F4 | XII | 11487 | T | between YLL066C and YLL065W, 550 bases from ACS in X repeat |
| F47 | X | 483062 | Ty | within Ty1 element YJRWTy1-2 |
| F19 | XII | 796771 | NTy | within YLR333C, 127 bases from Ty1 insertion |
| F10 | IV | 309450 | D | between RPL13A and RPLA1 |
| F6 | VII | ∼330801 | D | between VPS45 and PAN2 |
| F36 | XI | 557166 | D | between YKR060W and KTR2 |
| F3 | XII | 830607 | D | between YLR351C and YLR352W |
| F37 | XIV | 317917 | D | between PSD1 and YNL168C |
| F9 | XV | 825909 | D | within YOR268C |
a
(T) Targeted insertions at the telomeres or HM loci; (NT) telomeric insertions that do not meet our definition for targeting; (R) insertions within the rDNA; (Ty) insertions within Ty elements; (NTy) insertions within 750 bases of a Ty element; (D) dispersed insertions with no apparent target specificity.