SYMPLASTIC SPERMATIDS (SYS) - A RECESSIVE INSERTIONAL MUTATION IN MICE CAUSING A DEFECT IN SPERMATOGENESIS

被引:64
作者
MACGREGOR, GR
RUSSELL, LD
VANBEEK, MEAB
HANTEN, GR
KOVAC, MJ
KOZAK, CA
MEISTRICH, ML
OVERBEEK, PA
机构
[1] SO ILLINOIS UNIV, SCH MED, DEPT PHYSIOL, STRUCT BIOL LAB, CARBONDALE, IL 62901 USA
[2] UNIV TEXAS, MD ANDERSON HOSP & TUMOR INST, CTR CANC, DEPT EXPTL RADIOTHERAPY, HOUSTON, TX 77030 USA
[3] NIAID, MOLEC MICROBIOL, BETHESDA, MD 20892 USA
关键词
mouse chromosome 14; transgenic mice;
D O I
10.1073/pnas.87.13.5016
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A line of transgenic mice that carries an insertional mutation in a gene essential for spermatogenesis is described. Males homozygous for the transgenic insert are sterile, while female homozygotes and both male and female heterozygotes exhibit normal fertility. Developing spermatids in homozygous males form prominent abnormal multinucleated syncytia (symplasts) and do not complete maturation. In addition, abnormal cytoplasmic vacuolation is commonly seen in Sertoli cells. One flank of the transgenic integration site within the genome has been cloned and used to show linkage between homozygosity for the transgene and the mutant phenotype. The flank maps to mouse chromosome 14 approximately 4 centimorgans proximal to the gene encoding esterase-10 (Es-10). As no other gene that is known to be essential for spermatogenesis has been mapped to this region of the genome and as the mutant phenotype is unique, the transgenic insert appears to affect a previously unidentified gene. We have named the mutation 'symplastic spermatids' (sys).
引用
收藏
页码:5016 / 5020
页数:5
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