Basal X chromosome segments present on Dp(1;Y)BSC chromosomes
Kim Cook, Russell Garton, Adam Brown, Megan Ward, Jennifer Deal, Megan Deal, Thom Kaufman & Kevin Cook
Bloomington Drosophila Stock Center
Indiana University
We have generated Y-linked duplications of X chromosomal segments by irradiating an attached-XY (C(1;Y)N12) with an inversion in the X chromosome. Irradiation produces a Dp(1;Y) chromosome by inducing a large deletion in the progenitor chromosome with one breakpoint within the inversion and another breakpoint in X heterochromatin or basal X euchromatin. The region distal to the deletion on a Dp(1;Y) consists of two parts: X tip genes distal to the inversion and genes from the middle of the X moved near the end of the X by the inversion. The distal and medial duplicated segments present on particular Dp(1;Y)BSC chromosomes have been described in other personal communications to FlyBase. 
The region of a Dp(1;Y) proximal to the deletion will carry no basal euchromatic genes if the proximal deletion breakpoint falls in X heterochromatin. When the proximal deletion breakpoint falls in basal X euchromatin, however, basal euchromatic genes will be present. This personal communication describes the basal X segments present on Dp(1;Y)s derived from In(1)BSC14, In(1)BSC17, In(1)BSC19, In(1)BSC26 and In(1)BSC33.
We mapped the distal extents of the basal segments to ~10 gene intervals defined by PCR primers using the following approach. Males carrying a Dp(1;Y) were crossed to females carrying a transposable element insertion in a basal X position. Primers flanking the insertion sites of the transposable elements were used to amplify fragments from DNA isolated from male progeny. With short extension times, fragments are amplified only if the site of the transposable element insertion is present on the Dp(1;Y). The following transposable elements and primer pairs were used in mapping:
Insertion: P{EPgy2}EY09781
Forward primer: CGCACAGGTCTTGAAGGCATTGCC ( X:21443126..21443149 )
Reverse primer: GTTTCTAGCAGCCCCCTTCGCACCG ( X:21443688..21443712 )
Insertion: P{Mae-UAS.6.11}CG14619GG01842
Forward primer: CATCGCTCGCGCGCACAATCTCGGC ( X:21858117..21858141 )
Reverse primer: GTGCCGCCAGGCTGTCTACGCTCC ( X:21858613..21858636 )
Insertion: P{GT1}BG01274
Forward primer: CTAGTGTATTTGCCTTCACCATAATCG ( X:21961730..21961756 )
Reverse primer: GAGCGAGGAATATCTGATATGCGG ( X:21962214..21962237 )
Insertion: PBac{WH}f02323
Forward primer: GATGGCGGTGTCCTTGTCTCTGGC ( X:22366703..22366726 )
Reverse primer: CCTGTGACATTAATGCAGGCGACGG ( X:22367213..22367237 )
The following basal segments are present on Dp(1;Y)s (Release 5 coordinates and predicted cytologies).  These Dp(1;Y)s carry basal euchromatic genes: 
Dp(1;Y)BSC190   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC191   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC199   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC200   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC201   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC211   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC245   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
Dp(1;Y)BSC240   X:21443126--21858117 ;h28--h29 (20A3-20C1;h28--h29)
PBac{WH}f02323, an insertion immediately distal to stnA in 20F3, was the most basal transposon insertion site we tested by PCR.  The following Dp(1;Y)s do not carry this insertion site and, consequently, do not duplicate basal euchromatic genes distal to stnA. 
Dp(1;Y)BSC228
Dp(1;Y)BSC229
Dp(1;Y)BSC230
Dp(1;Y)BSC232
Dp(1;Y)BSC233
Dp(1;Y)BSC234
Dp(1;Y)BSC236
Dp(1;Y)BSC238
Dp(1;Y)BSC239
Dp(1;Y)BSC241
Dp(1;Y)BSC242
Dp(1;Y)BSC243
Dp(1;Y)BSC244
Dp(1;Y)BSC246
Dp(1;Y)BSC247
Dp(1;Y)BSC248
Dp(1;Y)BSC249
Dp(1;Y)BSC250
Dp(1;Y)BSC251