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Tiêu đề Dmrt1 genes at the crossroads: a widespread and central class of sexual development factors in fish
Tác giả Amaury Herpin, Manfred Schartl
Trường học University of Wuerzburg
Chuyên ngành Physiological chemistry
Thể loại Minireview
Năm xuất bản 2011
Thành phố Wuerzburg
Định dạng
Số trang 10
Dung lượng 263,32 KB

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How-ever, a remarkable amount of descriptive expression data has been gathered in a large number of different fish species, particularly in the context of early gonadal development, gonad

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Dmrt1 genes at the crossroads: a widespread and central class of sexual development factors in fish

Amaury Herpin and Manfred Schartl

Physiological Chemistry I, University of Wuerzburg, Germany

Introduction

The phenomenon of two different sexes and

conse-quently the necessity to make a developmental decision

for an embryo to become male or female (the so-called

sex-determination process), and the further

differentia-tion of the whole organism into two distinct phenotypes,

are common throughout the animal, plant and fungi

kingdoms Nevertheless, with respect to animals at least,

decades of elegant genetic studies have led to the global

picture that the gene-regulatory cascades triggering

sexual differentiation from Caenorhabditis elegans and

Drosophilato mammals bear little resemblance to each

other Hence, although developmental cascades are

generally headed by highly conserved universal master

regulators that determine the developmental fate of

a cell lineage to a given tissue or organ during embryo-genesis, all the evidence suggests that sex determination might disobey the conventional rules of evolutionary conservation The common picture emerging here is that the genes at the top of the cascade are not conserved, whereas the downstream genes have homologues in a much broader spectrum of species [1,2] For example, SRY, the male sex-determining gene of mammals, has not been detected outside the eutherians (placental mammals) Conversely, known downstream effectors involved in gonadogenesis or gonadal differentiation like, for example, Wt1, Sox-9, Bmps and Amh (see [3] for a review) are present in all vertebrates including fish [4] and for most of them even in protostomes

Keywords

Dmrt1bY; Evolution; Gonad; Ovary; Sex

determination; Sex differentiation; Steroid

hormones; Teleost; Testis; transcriptional

regulation

Correspondence

A Herpin, University of Wuerzburg,

Physiological Chemistry, Am Hubland,

D-97074 Wuerzburg, Germany

Fax: +49 931 888 4150

Tel: +49 (0)931 888 4153

E-mail:

amaury.herpin@biozentrum.uni-wuerzburg.de

(Received 5 August 2010, revised 8

December 2010, accepted 25 January 2011)

doi:10.1111/j.1742-4658.2011.08030.x

A plethora of corroborative genetic studies led to the view that, across the animal kingdom, the gene-regulatory cascades triggering sexual develop-ment bear little resemblance to each other As a result, the common emerg-ing picture is that the genes at the top of the cascade are not conserved, whereas the downstream genes have homologues in a much broader spec-trum of species Among these downstream effectors, a gene family involved

in sex differentiation in organisms as phylogenetically divergent as corals, Caenorhabditis elegans, Drosophila, frogs, fish, birds and mammals is the dmrt gene family Despite the attention that Dmrt1 factors have received,

to date it has not been elucidated how Dmrt1s mediate their activities and putative downstream targets have yet to be characterized However, a remarkable amount of descriptive expression data has been gathered in a large variety of fish, particularly with respect to early gonadal differentia-tion and sex change This minireview aims at distilling the current knowl-edge of fish dmrt1s, in terms of expression and regulation It is shown how gonadal identities correlate with dimorphic dmrt1 expression in gonochoris-tic and hermaphrodigonochoris-tic fish species It is also described how sex steroid hor-mones affect gonadal identity and dmrt1 expression Emphasis is also given

to recent findings dealing with transcriptional, transcriptional, post-translational and functional regulations of the dmrt1a⁄ dmrt1bY gene pair

in medaka

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Among the downstream candidate genes, a gene

family involved in sex differentiation in organisms as

phylogenetically divergent as C elegans, Drosophila,

frogs, fish, birds, mammals and corals is the dmrt gene

family [5] The prototype members of this group of

factors are the Drosophila doublesex (dsx) and

Caenor-habditis mab-3 genes The Dmrt group of molecules is

characterized by a conserved DNA-binding motif

known as the Doublesex- and Mab-3-related (DM)

domain Being a noncanonical cysteine-rich

DNA-binding motif, this domain has two highly intertwined

finger structures that chelate one zinc ion each, and

binds to the minor groove of the DNA [6] Dmrts were

originally described to play important roles during sex

determination in flies and worms by regulating several

aspects of somatic sexual dimorphism They were also

reported to be able to substitute for each other across

species, indicating that their function is possibly

inter-changeable and that sex determination in invertebrates

might rely on conserved molecules, at least at the

bot-tom of the cascade [7] Consistently, many of the

sub-sequently characterized metazoan Dmrt homologues

were predominantly expressed in the developing

gonads Thus, this widespread class of factors

com-monly appeared to be directly involved in sex

determi-nation Although homology relationships of dmrt gene

family members across all the metazoans have not

been established, for vertebrates it has been shown that

the prototype member of the gene family, designated

dmrt1, is most closely related to the Drosophila dsx

and C elegans mab-3 genes in structure and by means

of sex-determination⁄ differentiation function Gonadal

dmrt1 expression is generally detected at higher levels

in testes than ovaries

The deep interest in Dmrt1 in the field of sex

deter-mination in fish came with the discovery of a dmrt1

homologue on the Y chromosome of the fish medaka

(Oryzias latipes) This Y-chromosomal gene is the

product of a gene duplication of the autosomal dmrt1a

gene and was designated dmrt1bY [8] or Dmy [9] It

was shown to be the only functional gene in the whole

Y-specific region of the sex chromosome [10]

Muta-tions affecting this gene result in male-to-female sex

reversal [11] In addition, dmrt1bY transgene-induced

testis development in genetic females (XX) definitively

pointed out that it is not only necessary, but also

suffi-cient for triggering male development [12] Considering

that dmrt1bY has all the features of the master

regula-tor of testicular differentiation in medaka (see [13] for

review) and because of the discovery of

sex-chromo-some-linked dmrt1s in other vertebrates (DM-W in

Xenopus [14] and dmrt1 in birds [15] for example),

it was tempting to speculate, at least for teleosts,

that dmrt1s might have a universal and top control function during sex determination However, the absence of a dmrt1bY gene even in closely related Medaka species ruled this out [16] Nevertheless, factu-ally it did not exclude Dmrt1, in general, as an impor-tant conserved effector of testis development, including spermatogenesis

Despite the attention that Dmrt1 factors have received, to date it has not been elucidated how Dmrt1s mediate their activities and putative down-stream targets have yet to be characterized [17] How-ever, a remarkable amount of descriptive expression data has been gathered in a large number of different fish species, particularly in the context of early gonadal development, gonadal differentiation and sex change This minireview aims at distilling current knowledge about the expression and regulation of dmrt1s in fish towards a more general picture Emphasis is also given

to recent findings dealing with transcriptional, post-transcriptional, post-translational and functional regu-lation of the dmrt1a⁄ dmrt1bY gene pair in medaka

Gonadal dmrt1 gene expression across different fish species

An amazing variety of sex-determining systems is found in fish Although information is emerging about sex determination in lampreys, sharks, rays and stur-geons, most of our knowledge stems from studies on teleost fish Hence, this minireview mainly concentrates

on that group A considerable number of teleost spe-cies are hermaphrodites, switching either from first being males (protandrous) to become female or vice versa (protogynous) Nevertheless, the majority of tele-osts are gonochoristic, meaning that they exist as males and females regardless of the primary sex deter-mination initiating process being environmental (temperature, social) or genetic (XY or ZW)

Gonadal dimorphic dmrt1 expression

in gonochoristic species

Male-restricted expression of dmrt1 has been reported for North African catfish Clarias gariepinus [18], rare minnow Gobiocypris rarus [19], Nile tilapia Oreochr-omis niloticus [20], medaka Oryzias latipes [21] and olive flounder Paralichthys olivaceus [22] In lake stur-geon Acipenser fulvescens [23], zebrafish Danio rerio [24], Atlantic cod Gadus morhua [25], pejerrey Odontes-thes bonariensis [26], rainbow trout Oncorhynchus mykiss [27], shovelnose sturgeon Scaphirhynchus plato-rynchus [28] and southern catfish Silurus meridionals [29] a strong male-biased expression appears as the

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general rule, although some dmrt1 expression could be

detected in ovaries (see Table 1) Interestingly, when

detected in the ovary, dmrt1 expression is consistently

seen in the germ cells (Gadus morhua [25] and

Danio rerio [24]), whereas much broader and less

restricted expression territories are seen within the

tes-tis With respect to a gonadal function of Dmrt1, its

early expression in the somatic part of the male gonad

anlage (Oreochromis niloticus [20] and Oryzias latipes

[21]) would infer a role correlated with Sertoli cell

lineage specification and subsequently during testicular

differentiation The specific expression in spermatogo-nia and spermatocytes reported for Clarias gariepinus [18], Danio rerio [24] and Gadus morhua [25] are clearly consistent with a role at some stage of spermatogenesis

in these species

Another remarkable piece of information towards the understanding of Dmrt1 function(s) is coming from gonochoric fish that are annual breeders (Clarias gariepinus [18], Oncorhynchus mykiss [27] and Silurius meridionalis [29]) In these species, fish undergo a sea-sonal pattern of gonadal resting and recrudescence

Table 1 Gonadal expression of dmrt1 genes across the fish kingdom.

Species

Gonadal expression Expression levels

Expression

spermatocytes

PCR, IC, western blot

[18]

spermatocytes spermatids and developing oocytes

spermatocytes

PCR, IC, western blot

[32]

spermatogenesis

Germ cells (testis and ovary)

Monopterus albus pG Testis, ovotestis

and ovary (sex-specific splice variants

High in testes Gonadal epithelium,

undifferentiated germ cells (splice variants)

PCR, ISH, Northern blot

[34]

Odontesthes bonariensis TSD Primordial gonads During testicular

differentiation

Oncorhynchus mykiss G Testis and ovary Higher in testes Differentiating testis PCR, Northern

blot

[27] Oreochromis niloticus G Testis In sex-reversed testes Sertoli and epithelial cells

of the efferent duct

supporting cells, pre-Sertoli,

PCR, ISH, IC [21,54]

interstitial tubules

Scaphirhynchus

platorynchus

testicular involution

Silurus meridionalis G Ovary and testis High in testes during

masculinization

Sertoli cells

G, gonochoric; pA, protandrous; pG, protogynous; TSD, temperature-dependent sex determination; n.i., not investigated; IC, immunocyto-chemistry; ISH, in situ hybridization.

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rather than being continuously mature individuals In

general, for males, abundant dmrt1 expression during

preparatory and prespawning and spermatogenesis

periods was seen, in contrast to a gradual decrease

thereafter during spawning⁄ spermination This

indi-cates that dmrt1 may have an important role

during testicular recrudescence and particularly during

spermatogenesis

Hence, for all gonochoristic fish species investigated

to date, the dmrt1 expression pattern was always

shown to be intimately linked to male gonadogenesis

and further differentiation (Table 1)

Dmrt1 expression in protogynous and

protandrous hermaphroditic species

In hermaphrodite fish (protogynous or protandrous),

the developmental pathways leading to either testicular

or ovarian establishment have to be plastic and

suscep-tible to the sex-inversion signals considerably beyond

embryogenesis and early larval stages, whereas in

gonochoristic species the developmental decision

towards male or female is finally and irreversibly taken

long before adulthood is reached In this context,

dmrt1 expression dynamics were consistently shown to

parallel either the development (protogynous; black

porgy Acanthopagrus schlegeli [30], gilthead seabream

Sparus auratus [31]) or regression (protandrous;

grouper Epinephlus coioides [32], wrasse

Halicho-eres tenuispinis [33], rice field eel Monopterus albus

[34]) of the testes This confirms the abovementioned

role during testicular development and⁄ or

spermato-genesis Of note, in pejerrey (Odontesthes bonariensis),

a teleost with a temperature-dependant sex

determina-tion system, developmental expression of dmrt1 is

perfectly correlated with the rearing temperature (up at

male-determining temperatures and down at

female-determining temperatures) [26]

Dmrt1 expression in fish and other

vertebrates, what does it tell us?

In some fish species, dmrt1 expression is seen only in

somatic cells, whereas other fish have clearly additional

expression in the germ cell lineage (Table 1) This

dif-ference in cell types expressing dmrt1 might reflect

spe-cies-specific differences in testicular structure and

development A dual dmrt1 cell lineage expression in

Sertoli and germ cells is the hallmark of mammalian

dmrt1s Surprisingly, although mouse dmrt1 is detected

in the bipotential gonad, knockout male mice have

defects only during postnatal testis differentiation [35]

Although this observation might lead to the

assump-tion that germline expression is dispensable, condi-tional dmrt1 inactivation in either the Sertoli cells or the germ cells indicated that mouse Dmrt1 is indeed required for radial migration of germ cells and survival

of gonocytes It is also required autonomously for proper Sertoli cell differentiation [36] Hence, it is seen that mouse Dmrt1 might not play a major role during early testis differentiation, but rather appears to be required later for male gonadal differentiation Inter-estingly, also expressed in the primordial gonads at the time of sex determination, the Z-linked dmrt1 gene

in chicken [15, 37] and the W-linked DM-W gene in frog [14, 38] have been shown to be the major male and female determinants, respectively Altogether, it appears that when earlier in the cascade of sex deter-mination, the role of Dmrt1 is first to be an inducer of sex determination Later on, when still or only expressed at later stages after the gonad is formed and being by implication at a more downstream position within the cascade, its task is restricted to a mainte-nance function essentially in Sertoli cells

Other dmrt genes expressed in the fish gonads

The developmental expression of dmrt1 has been well studied in the context of gonadal induction and main-tenance, illuminating its important function But what about the other dmrt genes? Table 2 summarizes the expression pattern of these genes in fish during devel-opment and in the gonads Although less-extensively studied, two main tendencies can already be deduced from these data First, fish dmrt family members (Dmrt2, -3, -4, -5) exhibit conserved expression during the earliest stages of embryonic development in various organs, including the undifferentiated gonads Second, later during development, these genes usually remain expressed in a subset of adult organs including spinal cord, brain and gonads Noteworthy, male-specific gonadal expression could be observed for dmrt3 in medaka [39] and dmrt4 in medaka [39] and olive floun-der [40] (Table 2) By contrast, in tilapia dmrt4 expres-sion is exclusively detected in the ovary [41] Finally, both male and female gonadal expression was reported for dmrt2 in medaka [39] and dmrt3 and -5 in zebrafish [42,43] This expression discrepancy regarding the dmrt paralogues may indicate a possible functional switch between those in different phylogenetic lineages Remarkably, when reported, non-dmrt1 gene expres-sion generally occurs in developing germ cells (Table 2)

In terms of inferred function(s), this incidentally indi-cates that paralogs of dmrt1 in fish, although obviously not involved in the first steps of gonadogenesis, might

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be implicated in the later processes leading to the

proper development of germ cells

Effects of sex steroid hormones on

gonadal identity and dmrt1 expression

Sex steroids have local, direct effects on germ cell

development, but also act as endocrine hormones to

influence other cell types and organs involved in sex

differentiation This multilevel control is especially

complex in fish and involves a multitude of

biochemi-cal and physiologibiochemi-cal pathways to provide the

neces-sary plasticity for gonadal development (see [4] for

review) In that context, understanding the changes in

dmrt1 expression following steroid treatment is of

prime interest in order to link the molecular cellular

events with the extracellular hormonal signalling

sys-tem in gonad development

Studies employing fish exposed to estrogens (or

sub-stances mimicking estrogen activities) are sparse but

consistent in the reported effects on dmrt1 regulation

(Fig 1) In rare minnow [19], pejerrey [26] and

zebra-fish [44], estrogen exposure resulted in cessation of

male gonad development and sex reversal This was

always correlated with a pronounced decrease in dmrt1

mRNA levels Of note, in the same conditions,

rain-bow trout dmrt1 expression was only slowly inhibited

[45], indicating that a reduced permissive amount of

Dmrt1 expression might not be totally incompatible

with active ovarian differentiation In addition, in

pejerrey, a fish with strong temperature-dependant sex

determination, by combining different raising

tempera-tures with E2 treatments, Fernandino et al [26] could

surmise that low dmrt1 and high cyp19a1a (aromatase)

expression is connected to ovarian differentiation,

whereas the opposite is true for testicular

develop-ment Furthermore, in females, cyp19a1a expression

increased 1 and 2 weeks before the onset of dmrt1 and

the first morphological signs of ovarian differentiation respectively, suggested that biologically active estrogen regulates dmrt1 expression [26]

Neurohormones (GnRHa) and either androgens, aro-matase inhibitors or estrogen receptor antagonists have been shown to be very potent in manipulating the sexual phenotype of fish [4] (Fig 1) These treatments, when applied to gonochoristic or hermaphroditic species, always resulted in a clear morphological masculinization process correlated with Dmrt1 upregulation (Fig 1) Of note, some studies also pointed out the concomitant downregulation of cyp19a1a expression [46,47] It then appears that dmrt1 could be one of the major regulators upstream of this enzyme in fish It could be shown in trout that masculinizing treatments (1,4,6-androstatri-ene-3,17-dione) were inducing rapid and strong tran-scriptional upregulation of testicular markers like dmrt1, dax1 and pdgfra [46] This upregulation was even interpreted as an essential step required for active mas-culinization Into that direction, Dmrt1 and Dax1 have recently been shown to directly downregulate cyp19a1a promoter activity in the fish ovary [47,48] Given the abovementioned observation that estrogens repress male differentiation it appears that, once initiated, factors of the male pathway downregulate the hormone Hence, a feedback loop between dmrt1, cyp19a1a, and by implica-tion the estrogen⁄ androgen balance, becomes apparent Dmrt1 expression modulation upon steroid treatments could then be a key effector of the induced gonadal identity change (Fig 1) Similarly, in chicken, it could

be shown that Dmrt1 also downregulates aromatase expression [37] Overall, it is now clear that, at least

in fish Dmrt1-regulating aromatase expression and by implication the estrogen⁄ androgen balance that would also feedback (negatively or positively respectively) on dmrt1 expression, creates a complex regulatory loop combining transcriptional regulation with steroid hor-monal activity (Fig 1) The main question remaining is

Table 2 Other dmrt genes having gonadal expression in fish.

pharyngeal arches and brain

[39]

Developing oocytes

Embryogenesis Olfactory placodes, neural tube

[43]

telencephalon, branchial arches

[39]

dmrt5 Danio rerio Testis (weak) and ovary (weaker):

both in developing germ cells

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whether this loop aims only at activating the male

path-way, or repressing the female one, or both

In zebrafish, the transcription factor Sox5, although

not itself sexually dimorphically expressed, was shown

to directly downregulate dmrt1 transcription during

development This, together with a possible negative

regulation of sox5 on cyp19a1a reported in the

red-spotted grouper (Epinephelus akaara) [49] (Fig 1),

would constitute a perfect core for the transcriptional

regulation network of dmrt1 and cyp19a1 in gonadal

development

Expression, regulation and functions

of dmrt1a/dmrt1bY in medaka

In the medaka, which has XY–XX sex determination,

dmrt1bY, the duplicated copy of dmrt1a on the Y

chromosome was shown to be the dominant master

regulator of male development [8], similar to Sry in mammals Although many of the earliest cellular and morphological events initiated by Sry have been char-acterized, little is known about how the initial molecu-lar activity of Sry is translated into cellumolecu-lar structure and organ morphology Interestingly, Dmrt1, the ancestor of Dmrt1bY, is one of the downstream effec-tors of Sry in the male pathway

In medaka, the duplicated copy of dmrt1 has acquired an upstream position in the sex-determining cascade Remarkably, this evolutionary novelty, which

is predicted to require a rewiring of the regulatory net-work, was brought about by co-option of ‘ready-to use’ pre-existing cis-regulatory elements carried by transposing elements Further, it was shown that Dmrt1bY was able to bind to one of these elements, called Izanagi, within its own promoter, leading to significant repression of its own transcription [50]

M A S C U L I N I Z A T I O N

F E M I N I Z A T I O N

Estrogen

Androgen/

Testosterone GnRHa

Aromatase inhibitor

Estrogen antagonist

Clarias gariepinus Silurius meridionalis Silurius meridionalis Acanthopagrus

E2 17-alpha/beta Estradiol 4-Nonylphenol

(Estrogen activity)

Odontesthes bonariensis Gobiocypris rarus

Oreochromis niloticus Epinephelus coioides Paralichthys olivaceus Oncorhynchus mykiss

Danio rerio

Dmrt1

Sox 5 + GATA

?

Androgen Estrogen

Cyp19a1a (aromatase) Cyp19a1a

?

D Epinephelus akaara D n i o r e r i o Oryzias latipes O r e h r o m i s n l o i u s

Fig 1 The fish dmrt1 regulatory network or the current knowledge of dmrt1 gene regulation in fish In many fish species, indirect dmrt1 transcriptional regulations have been described upon steroid treatment (Upper) Steroid-induced dmrt1 regulation Whereas feminizing sub-stances having an estrogen-like activity (4-Nonylphenol and 17-alpha ⁄ beta estradiol) lead to dmrt1 transcriptional downregulation, masculiniz-ing treatments (androgen, testosterone, aromatase inhibitors, estrogen antagonist or gnRHa) have been shown to conversely activate dmrt1 expression (Lower) Proven direct regulations affecting dmrt1 transcription In zebrafish, the transcription factor Sox5, although not itself sex-ually dimorphically expressed, was shown to directly downregulate dmrt1 transcription during development In addition, in medaka and tilapia direct Dmrt1 transcriptional activity was revealed by respectively downregulating dmrt1bY and Cyp19a1a promoter activities.

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(Fig 2) Interestingly, the autosomal Dmrt1a can bind

to this site Thus the Izanagi element enables the

self-and cross-regulation of dmrt1bY expression by Dmrt1

proteins (Fig 2) During the early stages, when the

pri-mordial gonad is determined towards testes, the

exclu-sively expressed Dmrt1bY alone exerts sex-determining

functions [9,51,52] Noticeably, during this same period

an 11-nucleotide protein-binding motif located in the

3¢-UTR of dmrt1bY mediates gonad-specific mRNA

stability [53] (Fig 2) This motif is conserved in the

3¢-UTRs of a wide range of dmrt1 orthologous genes

from flies to mammals, indicating that different

sys-tems may employ an evolutionary conserved RNA

regulatory mechanism for this gene [53]

Later during development of the juvenile fish and in the adult testes, where both dmrt1 genes have been shown to be expressed, it is of note that the newly gen-erated duplicate dmrt1bY is kept back under tight tran-scriptional regulation of the ancestral dmrt1a gene [53]

In addition to the transcriptional regulation events, it could be shown that at any developmental stages, Dmrt1bY protein was subject to an intensive turnover due to rapid degradation [54]

With respect to its biochemical function, Dmrt1bY and the other Dmrt1s also in fish appear to act as transcription factors This is evident from the nuclear localization of Dmrt1 fusion proteins [54,55] and stud-ies showing direct effects of Dmrt1 on reporter gene expression as well as binding to a cognate motif in electric mobility shift assays [47,50]

Finally, linking the earliest sexual dimorphic trait

to its expression dynamic, Dmrt1bY was shown to be possibly responsible for the male-specific primordial germ cell mitotic arrest [55] (Fig 2) Indeed, functional evidence showed that expression of Dmrt1bY leads to negative regulation of male primordial germ cell prolif-eration prior to sex determination at the sex-determi-nation stage [55] This suggests that in XY medaka males, Dmrt1bY-driven primordial germ cell number regulation, as well as determination of pre-Sertoli cells,

is the primary event by which the whole gonad (germ-line and soma) would be specified through a direc-tional cross-talk from pre-Sertoli and Sertoli cells with the primordial germ cells Interestingly, at this point, a parallel can be drawn with Dmrt1 function studies in mice The lack of dmrt1 in mutant mice caused a high incidence of teratomas and resulted in a failure of germ cells to arrest mitosis [56] Thus, Dmrt1 in mice and similarly Dmrt1bY in medaka appear to be regu-lators of germ cell proliferation

Conclusion

To conclude, it seems that the longstanding hypothesis suggesting that the molecular sequence of sex-determi-nation cascades might disobey the conventional rules

of evolutionary developmental is now very well sup-ported experimentally by data gathered in fish Indeed, regarding Dmrt1, it is now obvious that because of consistent expression patterns in the gonads, and although necessarily acting at different stages of the sex-determining cascade, these effectors must individu-ally fulfil similar and highly conserved functions Hence, beyond the fish sphere, data recently published

in Xenopus and chicken (see [14, 15] this minireview series) about dmrt genes being demonstrated to be of first importance for gonadal determination support the

Transcriptional

regulation

Post-transcriptional

regulation

Post-translational

regulation

progression

Fig 2 Medaka dmrt1a ⁄ dmrt1bY regulations and functions Grey

arrows illustrate the different levels for which active

dmrt1a ⁄ dmrt1bY regulation mechanisms could be shown

Tran-scriptional regulation: the feedback autoregulation of dmrt1bY

promoter activity and transregulation by its paralogue Dmrt1a is a

key mechanism of dmrt1bY transcriptional tuning

Post-transcrip-tional regulation: a highly conserved cis-regulatory motif directs

dif-ferential gonadal synexpression of dmrt1 transcripts during gonadal

development Post-translational regulation: Dmrt1a and Dmrt1bY

have a short half-life and consequently a high turnover Functions:

Dmrt1bY inhibition of germ cell proliferation might be part of its

known male determining function.

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scheme that, whatever the sex-determination system,

more comparative studies of dmrt1 are required in

order to draw the first lines of a global core regulatory

network for sex determination

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