An SD chromosome is capable of causing efficient distortion in two Rspss bearing chromosomes within a spermatocyte nucleus.
super sensitive
M(Sd)[+]/M(SD)1, Rspss has male fertile phenotype
M(Sd)[+]/M(SD)1, Rspss/Rspi has male fertile phenotype
M(Sd)[+]/M(SD)1, Rspss/Rsps has male fertile phenotype
M(Sd)[+]/M(SD)1, Rspss/Rspsi has male fertile phenotype
M(SD)1, Rspss has male fertile phenotype
M(SD)1, Rspss/Rspi has male fertile phenotype
M(SD)1, Rspss/Rsps has male fertile phenotype
M(SD)1, Rspss/Rspsi has male fertile phenotype
RanGAPβTub85D.PK causes very strong segregation distortion in the presence of the "SD-5[R7]" chromosome (E(SD)1, Rspi, M(SD)1, St(SD)1) over a target homolog chromosome carrying Rspss. Segregation distortion does not occur if the target homolog chromosome carries Rspi in place of Rspss. Overexpression of RanGAPβTub85D.PK does not cause segregation distortion in the presence of the "SD-5[R16]" chromosome (which carries a strong suppressor of SD in addition to RanGAPSd, E(SD)1, Rspi, M(SD)1, St(SD)1) over a target homolog chromosome carrying Rspss. RanβTub85D.PK and Rcc1βTub85D.PK can both suppress the segregation distortion phenotype caused by RanGAPβTub85D.PK in the presence of the "SD-5[R7]" chromosome (E(SD)1, Rspi, M(SD)1, St(SD)1) over a target homolog chromosome carrying Rspss.
Temin and Marthas.
Associated with: In(2R)NS.