From: The ribosomal protein genes and Minute loci of Drosophila melanogaster
CRP genea | Genetic analysisb | Â | Â | Â | Â | |||
---|---|---|---|---|---|---|---|---|
Symbol | Location | CRP gene mutationsc, d | Deletions removing a single CRP genec, e | Other evidence | Is the CRP gene a Minute?f | No. of candidate Minute genesg | Minute synonymh | Referencei |
X chromosome | Â | Â | Â | Â | Â | Â | Â | Â |
   RpL36 | 1B12 |  | M |  | Yes |  | M(1)1B | [53] |
   RpL22 | 1C4 | + | + |  | No |  |  |  |
   sta/RpSA | 2B1 | + | + |  | No |  |  |  |
   RpL35 | 5A11 |  |  | Lies in a gap in deletion coverage. 5A6-13 aneuploids were Minute (Merriam et al. [55]) | Likely | 33 | M(1)5A |  |
   RpL7A | 6B1 |  | M |  | Likely | 2 | M(1)5D6A |  |
   RpL17 | 6C10 |  |  | Lies in a gap in deletion coverage | Likely | 12 | New? |  |
   RpS6 | 7C2 | M | M |  | Yes |  | M(1)7BC and M(1)7C | [2] |
   RpS14a | 7C6-7 |  |  | A deletion that removes RpS14a and RpS14b is not Minute [95] | No |  |  |  |
   RpS14b | 7C8 |  |  | A deletion that removes RpS14a and RpS14b is not Minute [95] | No |  |  |  |
   RpS28b | 8E7 |  |  | Lies in a gap in deletion coverage. A Minute mutation was mapped to 8D8-9A2 [153] | Likely | 17 | M(1)8F |  |
   RpS15Aa | 11E11-12 |  | M |  | Likely | 8 | M(1)11F |  |
   RpL37a | 13B1 |  |  | Lies in a gap in deletion coverage. 12F6-13B6 aneuploids were Minute (Merriam et al. [55]) | Likely | 2 | M(1)13A |  |
   RpS19a | 14F4 |  | M |  | Likely | 14 | M(1)14E |  |
   RpS5a | 15E5-7 | M |  | Lies in a gap in deletion coverage | Yes |  | M(1)15D | [44] |
   RpS10b | 18D3 | M | M |  | Yes |  | M(1)18C |  |
Chromosome arm 2L | Â | Â | Â | Â | Â | Â | Â | Â |
   RpLP1 | 21C2 | M | M |  | Yes |  | M(2)21C | [50] |
   oho23B/RpS21 | 23B6 | M | M |  | Yes |  | M(2)23B | [49] |
   RpL40 | 24E1 |  | M |  | Likely | 4 | M(2)24D |  |
   RpL27A | 24F3 | M | M |  | Yes |  | M(2)24F |  |
   RpL37A | 25C4 |  | M | The interval between flanking non-Minute deletions contains only RpL37A | Yes |  | M(2)25C |  |
   RpL36A | 28D3 |  | M |  | Likely | 5 | M(2)28DE* |  |
   RpS13 | 29B2 | M | M |  | Yes |  | M(2)29B* | [45] |
   sop/RpS2 | 30E1 | + | + |  | No |  |  |  |
   RpL13 | 30F3 |  | M | The interval between flanking non-Minute deletions contains only RpL13 | Yes |  | M(2)31A |  |
   RpL7 | 31B1 |  | M |  | Likely | 2 | M(2)31A |  |
   RpS27A | 31E1 |  | M |  | Likely | 6 | M(2)31E* |  |
   RpL9 | 32C1 | M | M |  | Yes |  | M(2)32D | [46] |
   RpL24 | 34B10 |  | M |  | Likely | 8 | M(2)34BC* |  |
   RpS26 | 36F4 | M | M |  | Yes |  | M(2)36F |  |
   RpL30 | 37B9 | + | + |  | No |  |  |  |
   RpL21 | 40A-B |  | M |  | Likely | 10 | M(2)39F |  |
   RpL5 | 40B | M | M |  | Yes |  | M(2)40B* | [51] |
Chromosome arm 2R | Â | Â | Â | Â | Â | Â | Â | Â |
   RpL38 | 41C-E | M | M |  | Yes |  | M(2)41A | [51] |
   RpL31 | 45F5 | M |  | Lies in a gap in deletion coverage | Yes |  | M(2)45F* |  |
   RpS15Ab | 47C1 |  | + |  | No |  |  |  |
   RpS11 | 48E8-9 | M |  | Lies in a gap in deletion coverage | Yes |  | M(2)48E* |  |
   RpS23 | 50E4 |  | M |  | Likely | 2 | M(2)50E* |  |
   RpS15 | 53C8 |  |  | M(2)531 Minute phenotype rescued by duplication of 51F-54A [154] but not by a RpLP2 transgene [155] | Likely | 16 | M(2)53 |  |
   RpLP2 | 53C9 |  | M |  | Likely | 5 | M(2)53 |  |
   RpL18A | 54C3 |  |  | Lies in a gap in deletion coverage | Likely | 16 | New? |  |
   RpL11 | 56D7 |  |  | Lies in a gap in deletion coverage. 56C-D aneuploids were Minute [55] | Likely | 3 | M(2)56CD |  |
   RpS18 | 56F11 |  | M |  | Likely | 2 | M(2)56F |  |
   RpL29 | 57D8 |  | + |  | No |  |  |  |
   RpS16 | 58F1 |  |  | Deletions that remove both RpS16 and RpS24 are Minute. The Minute mutations M(2)58F1 and RpS24SH2053 complement, suggesting RpS16 is a Minute gene | Likely | 25 | M(2)58F |  |
   RpS24 | 58F3 | M |  | Deletions that remove both RpS16 and RpS24 are Minute | Yes |  | M(2)58F |  |
   RpL23 | 59B3 |  | + |  | No |  |  |  |
   RpL37b | 59C4 |  | + |  | No |  |  |  |
   RpL12 | 60B7 |  |  | RpL12 and RpL39 lie in the same gap in deletion coverage. 60B3-10 aneuploids were Minute [156] | Likely | 9 | M(2)60B |  |
   RpL39 | 60B7 |  |  | RpL12 and RpL39 lie in the same gap in deletion coverage. 60B3-10 aneuploids were Minute [156] | Likely | 9 | M(2)60B |  |
   RpL41 | 60E5 | + | + |  | No |  |  |  |
   RpL19 | 60E11 | M |  | A deletion that removes RpL19 and RpL41 is Minute | Yes |  | M(2)60E | [42] |
Chromosome arm 3L | Â | Â | Â | Â | Â | Â | Â | Â |
   RpL23A | 62A10 |  | M |  | Likely | 8 | M(3)62A |  |
   RpL8 | 62E7 |  |  | Lies in a gap in deletion coverage containing only RpL8. 62E-63A aneuploids were Minute [54] | Yes |  | M(3)62F |  |
   RpL28 | 63B14 |  | M |  | Likely | 10 | M(3)63B |  |
   RpL18 | 65E9 |  | M |  | Likely | 8 | M(3)65F |  |
   RpL14 | 66D8 | M |  | Lies in a gap in deletion coverage | Yes |  | M(3)66D | [47] |
   RpS17 | 67B5 |  |  | A deletion removing both RpS17 and RpS9 is Minute. The unsequenced Minute mutations RpS174 and RpS176 complement the Minute mutation RpS9EP3299, suggesting RpS17 is a Minute gene | Likely | 13 | M(3)67C |  |
   RpS9 | 67B11 | M |  | A deletion removing both RpS17 and RpS9 is Minute | Yes |  | M(3)67C |  |
   RpL10Ab | 68E1 |  | + |  | No |  |  |  |
   RpS12 | 69F5 |  | + | A deletion that removes RpS12 and RpS4 is Minute | No |  |  |  |
   RpS4 | 69F6 |  |  | A deletion that removes RpS12 and RpS4 is Minute | Likely | 2 | M(3)69E |  |
   RpL26 | 75E4 |  | + |  | No |  |  |  |
   RpLP0 | 79B2 | + | + |  | No |  |  |  |
   Qm/RpL10 | 80A |  | M |  | Likely | 23 | M(3)80 |  |
   RpL15 | 80F |  | M |  | Likely | = 11 | M(3)80F* |  |
Chromosome arm 3R | Â | Â | Â | Â | Â | Â | Â | Â |
   RpL35A | 83A4 |  |  | Lies in a gap in deletion coverage | Likely | 3 | New? |  |
   RpL13A | 83B6-7 | M |  | Lies in a gap in deletion coverage | Yes |  | M(3)83B* | [52] |
   RpL34b | 85D15 |  |  | Lies in a gap in deletion coverage | Likely | 3 | New? |  |
   RpS29 | 85E8 | M | M |  | Yes |  | M(3)85E |  |
   RpS25 | 86D8 |  |  | A deletion that removes RpS25 and RpL3 is Minute | Likely | 14 | M(3)86D |  |
   RpL3 | 86D8 | + |  |  | No |  |  |  |
   RpS5b | 88D6 | + | + |  | No |  |  |  |
   RpL10Aa | 88D10 |  | + |  | No |  |  |  |
   RpS20 | 93A1 |  |  | A deletion that removes RpS20 and RpS30 is Minute | Likely | 21 | M(3)93A* |  |
   RpS30 | 93A2 |  |  | A deletion that removes RpS20 and RpS30 is Minute | Likely | 21 | M(3)93A* |  |
   RpS3 | 94E13 | M | M |  | Yes |  | M(3)95A | [43] |
   RpS19b | 95C13 |  | + |  | No |  |  |  |
   RpS27 | 96C8 |  | M |  | Likely | 5 | M(3)96C |  |
   RpL27 | 96E9-10 |  | M |  | Likely | 6 | M(3)96CF |  |
   RpL34a | 96F10 |  | + |  | No |  |  |  |
   RpS10a | 98A14 |  | + |  | No |  |  |  |
   RpL4 | 98B6 |  | M |  | Likely | 6 | M(3)98B* |  |
   RpS8 | 99C4 |  |  | Lies in a gap in deletion coverage. 99B aneuploids were Minute [157] | Likely | 11 | M(3)99B |  |
   RpS28a | 99D2 |  |  | The Minute phenotype of a deletion removing RpS28a and RpL32 is rescued by a RpL32 transgene [41] | No |  |  |  |
   RpL32 | 99D3 |  |  | The Minute phenotype of a deletion removing RpS28a and RpL32 is rescued by a RpL32 transgene [41] | Yes |  | M(3)99D | [41] |
   RpS7 | 99E2 |  |  | Lies in a gap in deletion coverage. 99E-F aneuploids were Minute [157] | Likely | 11 | M(3)99E |  |
   RpL6 | 100C7 |  |  | Lies in a gap in deletion coverage. 100C-F aneuploids were Minute [157] | Likely | 16 | M(3)100CF |  |
Chromosome 4 | Â | Â | Â | Â | Â | Â | Â | Â |
   RpS3A | 101F1 | M | M |  | Yes |  | M(4)101 | [48] |