Sequencing
SFAF2016%20Meeting%20Guide%20Final%203
SFAF2016%20Meeting%20Guide%20Final%203
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
11th Annual <strong>Sequencing</strong>, Finishing, and Analysis in the Future Meeting<br />
CHARACTERIZING CHROMOSOMAL<br />
TRANSLOCATIONS ASSOCIATED WITH A GENETIC<br />
SEXING SYSTEM<br />
Friday, 3rd June 12:40 La Fonda Ballroom Talk (OS‐8.04)<br />
Scott Geib 1 , Sheina Sim 2<br />
1 USDA‐ARS DKI US PBARC, 2 University of Hawaii, Manoa<br />
The Mediterranean fruit fly (medfly) is an important agricultural pest of many fruit and vegetable<br />
species. To protect the mainland United States from this pest, the sterile insect technique (SIT) is<br />
employed, involving release of tens of millions of sterile male medfly into the Los Angeles basin of<br />
California weekly. These flies have several mutations making them amenable to mass release. Due<br />
to a chromosomal translocation between the 5th chromosome and the male Y chromosome, females<br />
are homozygous recessive for both a temperature sensitive lethal mutation and a white pupal<br />
mutation, allowing straightforward separation of male and female flies and generation of male only<br />
release strains. Heterozygosity for these loci is maintained in males through the chromosomal<br />
translocation, linking wild‐type phenotype with the sex chromosome. Utilizing several different<br />
sequenced based approaches, we compare the utility of these techniques to identifying the location<br />
of the Y‐A translocation in this species. Structural variation was determined utilizing Hi‐C (3C‐seq)<br />
libraries, 10X genomics GemCode libraries and a high‐density SNP based genetic maps derived from<br />
test crosses from both wild‐type and translocated lab lines. In addition, scaffolding approaches<br />
utilizing these library types individually, as well as in combination with each other, are investigated<br />
for generating chromosome‐scale genomic assemblies at a low cost.<br />
141