Somatic hybridization is performed to obtain significant cytoplasmic male sterility(CMS) lines, whose CMS genes are derived either from the transfer of sterile genes from the mitochondrial genome of donor parent to the counterpart of receptor or production of new sterile genes caused by mitochondrial genome recombination of the biparent during protoplast fusion. In this study, a novel male sterile line, SaNa-1A, was obtained from the somatic hybridization between Brassica napus and Sinapis alba. The normal anther development of the maintainer line, SaNa-1B, and the abortive process of SaNa-1A were described through phenotypic observations and microtome sections. The floral organ of the sterile line SaNa-1A was sterile with a shortened filament and defl ated anther. No detectable pollen grains were found on the surface of the sterile anthers. Semi-thin sections indicated that SaNa-1A aborted in the pollen mother cell(PMC) stage when vacuolization of the tapetum and PMCs began. The tapetum radically elongated and became highly vacuolated, occupying the entire locule together with the vacuolated microspores. Therefore, SaNa-1A is different from other CMS lines, such as ogu CMS, pol CMS and nap CMS as shown by the abortive process of the anther. Somatic hybridization is performed to obtain significant cytoplasmic male sterility (CMS) lines, whose CMS genes are derived either from the transfer of sterile genes from the mitochondrial genome of donor parent to the counterpart of receptor or production of new sterile genes caused by mitochondrial genome recombination of the biparent during protoplast fusion. In this study, a novel male sterile line, SaNa-1A, was obtained from the somatic hybridization between Brassica napus and Sinapis alba. The normal anther development of the maintainer line, SaNa-1B, and the abortive process of SaNa-1A ​​were described through phenotypic observations and microtome sections. The floral organ of the sterile line SaNa-1A ​​was sterile with a small anthers. No detectable pollen grains were found on the surface of the sterile anthers. Semi -thin sections indicated that SaNa-1A ​​aborted in the pollen mother cell (PMC) stage when vacuolization of the tapetum and PMCs began. The tapet um radically elongated and became highlyomedlated, occupying the entire locule together with the vacuumed microspores. Thus SaNa-1A ​​is different from other CMS lines, such as ogu CMS, pol CMS and nap CMS as shown by the abortive process of the anther.