Tsx Produces a Long Noncoding RNA and Has General Functions in the Germline, Stem Cells, and Brain

被引:186
作者
Anguera, Montserrat C. [1 ,2 ,3 ]
Ma, Weiyuan [4 ,5 ]
Clift, Danielle [1 ,2 ,3 ]
Namekawa, Satoshi [6 ]
Kelleher, Raymond J., III [4 ,5 ]
Lee, Jeannie T. [1 ,2 ,3 ]
机构
[1] Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[4] Massachusetts Gen Hosp, Ctr Human Genet Res, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[6] Cincinnati Childrens Hosp Med Ctr, Div Reprod Sci, Cincinnati, OH USA
关键词
X-CHROMOSOME INACTIVATION; TESTIS-SPECIFIC GENE; SYNAPTIC PLASTICITY; MOUSE; TSIX; HIPPOCAMPUS; CHROMATIN; AMYGDALA; ANXIETY; REGION;
D O I
10.1371/journal.pgen.1002248
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The Tsx gene resides at the X-inactivation center and is thought to encode a protein expressed in testis, but its function has remained mysterious. Given its proximity to noncoding genes that regulate X-inactivation, here we characterize Tsx and determine its function in mice. We find that Tsx is actually noncoding and the long transcript is expressed robustly in meiotic germ cells, embryonic stem cells, and brain. Targeted deletion of Tsx generates viable offspring and X-inactivation is only mildly affected in embryonic stem cells. However, mutant embryonic stem cells are severely growth-retarded, differentiate poorly, and show elevated cell death. Furthermore, male mice have smaller testes resulting from pachytene-specific apoptosis and a maternal-specific effect results in slightly smaller litters. Intriguingly, male mice lacking Tsx are less fearful and have measurably enhanced hippocampal short-term memory. Combined, our study indicates that Tsx performs general functions in multiple cell types and links the noncoding locus to stem and germ cell development, learning, and behavior in mammals.
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页数:14
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