TABLE 2.
P-element insertion lines recovered in the investigation of the Hcf region
| Line | Eye color | P/P viable? | Event | Cytological position | Nucleotide position | Description of insertion site |
|---|---|---|---|---|---|---|
| 39C-12 starting line | Var | Yes | Jump from X chromosome | 102B5 | 380116 | Proximal of Hcf |
| 7-M201 | Red | Yes | Jump | 102B8 | 436566 | Proximal of lgs |
| 7-M547 | Red | No | Jump | 102C3 | 528024 | Within zfh2 |
| 7-M1015 | Red | No | Jump | 102C3 | 527838 | Within zfh2 |
| 7-M30 | Red | No | Deletion | 414195 | Distal to CG2052 | |
| 7-M972a | Red | No | Deletion | 414209 | Distal to CG2052 | |
| 7-M973a | Red | No | Deletion | 414209 | Distal to CG2052 | |
| 7-M1067a | Red | No | Deletion | 414209 | Distal to CG2052 | |
| 7-M369 | Red | Yes | Duplication | 376009 | Within CG2165 | |
| 7-M1148 | Red | Yes | Duplication | 90334 | Within pan | |
| 7-M484 | Var | No | Jump | 102C1 | 487401 | Distal of bip2 |
| 7-M1061 | Var | Yes | Jump | Unknown | Within 1360 | |
| 7-M1365 | Var | No | Jump | 102C1 | 487401 | Distal of bip2 |
| 7-M1399 | Var | Yes | Jump | 102B3 | 332186 | Proximal of CG2177b |
| 7-M53 | Var | No | Deletion | 479355 | Proximal to bip2 | |
| 7-M586 | Red | Yes | Duplication | ND | ||
| 7-M1244 | Red | Yes | Duplication | ND |
Nucleotide positions are given with reference to release 5.1 of the D. melanogaster genome sequence. Var, variegated; ND, not determined.
a
These lines were established from three siblings and most likely represent a single P-element-induced recombination event.
b
On the basis of inverse PCR results, the 7-M1399 insertion is located within a 1360 element adjacent to the nucleotide position listed in the table. However, on the basis of the published genome sequence, there is no 1360 element at this location, indicating that there has been a transposition event of 1360 in 7-M1399 or in the starting line.