The invention discloses a construction method of a Pnldc1
gene-deleted
spermatogenesis disorder mouse model, the Pnldc1
gene has a relationship with
spermatogenesis disorder or
fertility dysfunction, the volume of the testis of a Pnldc1
gene-deleted male mouse is significantly reduced compared with that of a wild mouse, the arrangement of seminiferous tubules in the testis of the male mouse is disordered, the number of long
sperm cells is reduced, and the seminiferous tubules in the testis of the male mouse are reduced. In the prior art, no
sperm exists in
epididymis, the head of a mouse
sperm is abnormal in development, 9 + 2 microtubules are deleted, and any
offspring cannot be obtained after the mouse is mated with a female mouse, gene editing is carried out in the early development stage of a fertilized egg, the obtained positive mouse is high in chimeric rate, and the passage probability is larger than that of a
blastocyst injection ES
cell. In addition, the invention can provide a better model for the research of male
sterility. Therefore, the male mouse with Pnldc1
gene deletion has the advantages of stability and thorough spermatogenic function inhibition.