Germ cell aneuploidy in zebrafish with mutations in the mitotic checkpoint gene mps1 - PubMed (original) (raw)

Germ cell aneuploidy in zebrafish with mutations in the mitotic checkpoint gene mps1

Kenneth D Poss et al. Genes Dev. 2004.

Abstract

Aneuploidy, resulting from chromosome missegregation during meiosis, is a major cause of human infertility and birth defects. However, its molecular basis remains incompletely understood. Here we have identified a spectrum of chromosome anomalies in embryos of zebrafish homozygous for a hypomorphic mutation in Mps1, a kinase required for the mitotic checkpoint. These aneuploidies are caused by meiotic error and result in severe developmental defects. Our results reveal Mps1 as a critical regulator of chromosome number in zebrafish, and demonstrate how slight genetic perturbation of a mitotic checkpoint factor can dramatically reduce the fidelity of chromosome segregation during vertebrate meiosis.

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Figures

Figure 1.

Figure 1.

Zebrafish homozygous for mps1zp1 generate dysmorphic offspring. (A) One-quarter to one-third of embryos from mps1zp1 parents appeared normal at 28 hpf (panel i). A significant proportion of embryos displayed head degeneration (panel ii, arrowhead), whereas others displayed severe defects in head, somite, and trunk development (panels iii,iv). In a small percentage of embryos, no head or trunk was distinguishable (panel v), or spectacular patterning defects were noted (panel vi). This embryo has two joined head and trunk structures in the absence of posterior structures (arrow-heads point to otic vesicles). (B) Frequency of dysmorphic progeny from different combinations of wild-type (+/+), mps1zp1 heterozygous (+/-), and mps1zp1 homozygous (-/-) parents. Data are shown as mean ± S.E.M. Student's _t_-test, (*) p formula image 0.001 versus two +/+ parents. (**) p formula image 0.001 versus two +/+ parents, p < 0.05 versus -/- father and +/+ mother. (***) p formula image 0.001 versus two +/+ parents, p formula image 0.001 versus -/- father and +/+ mother, p < 0.05 versus +/+ father and -/- mother. Numbers above the error bars represent the total number of dysmorphic embryos among the crosses, divided by the total number of embryos analyzed. The majority of mps1zp1 animals in these experiments were 7–10 mo of age. In our facilities, zebrafish retain fecundity from 4 to 15 mo of age, and live 2–3 yr.

Figure 2.

Figure 2.

mps1 is localized to immature zebrafish germ cells. (A) Northern analysis of mps1 expression using several adult tissues. RNA samples from testis and ovary, although slightly overloaded on this blot, are the only tissues that demonstrate mps1 expression. (B) In situ hybridization of ovarian tissue section detects strong mps1 expression (violet stain) in small, immature perinucleolar oocytes (p.o.). Mature vitellogenic oocytes (v.o.) show little or no mps1 expression. (C) In testis, mps1 mRNA is localized to primary and secondary spermatocytes (sc), with little or no expression in spermatozoa (sz). To confirm the identity of _mps1_-positive cells, animals were injected with BrdU 5 h prior to tissue processing. In 5 h, BrdU-positive cells (pink) result from mitotic division of spermatogonial stem cells to yield primary spermatocytes, or mitotic division plus one meiotic division to yield secondary spermatocytes. All BrdU-positive cells were also _mps1_-positive; mature spermatozoa were BrdU- and _mps1_-negative.

Figure 3.

Figure 3.

Mitotic checkpoint deficits and altered chromosome content in germ cells of male mps1zp1 zebrafish. (A) Confocal image of a meiotic cell from the testis of an mps1zp1 male treated for 12 h at 33°C, stained for γ-tubulin (red) and H3P (green). Arrowheads indicate two centrosomes. (B) Confocal image of two meiotic cells from the testis of an mps1zp1 male treated for 12 h at 33°C, stained for α-tubulin (red) and H3P (green). Each mitotic spindle has two clear poles (arrowheads). (C) Sections of testes from wild-type (top) and mps1zp1 (bottom) zebrafish treated with (left) or without (right) nocodazole for 12 h at 33°C, stained for α-tubulin (red) and H3P (green). Nocodazole treatment activates the mitotic checkpoint and induces arrest in wild-type animals, indicated by increases in meiotic cells, but has no effect in mps1zp1 clutchmates. (D) FACS analysis of sperm from representative wild-type (top) and mps1zp1 (bottom) males. mps1zp1 sperm displayed a wide range of size and DNA content (as assessed by propidium iodide fluorescence).

Figure 4.

Figure 4.

A high frequency of aneuploidy in mps1zp1 germ lines. (A) Eight-somite stage embryos (top), and representative FISH analyses (bottom) indicating one DAPI-stained nucleus for linkage groups 9 (red probe) and 17 (green). (Left) Wild-type embryo with elongated body, tapered tail, and normal head structure, is disomic for both linkage groups. (Center) mps1zp1 embryo with degenerated head and malformed trunk and tail, is trisomic for LG9. (Right) mps1zp1 embryo with blunted head and tail is monosomic for LG17. (B) Auto-radiograph indicating genotypes for genetic marker gof12 on LG17, from dysmorphic progeny of a representative wild-type male × mps1zp1 female cross. Each lane represents one embryo. The two parents of this family displayed four differently sized gof12 PCR products; red arrows indicate two alleles from the wild-type father, whereas blue arrows indicate two alleles from the mps1zp1 mother. Note two embryos with maternal LG17 monosomy (MO) and three with maternal LG17 trisomy (TR). (C) Meiotic nondisjunction rates of wild-type and mps1zp1 fathers and mothers in wild-type × mps1zp1 crosses. Data were compiled from analysis of 273 dysmorphic embryos from mps1zp1 fathers, and 197 dysmorphic embryos from mps1zp1 mothers. The numbers above the error bars represent the total number of losses (monosomy) or gains (trisomy) among five chromosomes analyzed, divided by the total number of chromosomes with informative polymorphisms. Student's _t_-test, (*) p formula image 0.001 versus wild-type male or female. (**) p formula image 0.001 versus wild-type male or female, p < 0.05 versus mps1zp1 father. All parents used for FISH and genotyping analyses were maintained at 25°C.

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