- Research article
- Open Access
Quantitative trait locus mapping of genes associated with vacuolation in the adrenal X-zone of the DDD/Sgn inbred mouse
BMC Genetics volume 13, Article number: 95 (2012)
Adrenal gland of mice contains a transient zone between the adrenal cortex and the adrenal medulla: the X-zone. There are clear strain differences in terms of X-zone morphology. Nulliparous females of the inbred mouse DDD strain develop adrenal X-zones containing exclusively vacuolated cells, whereas females of the inbred mouse B6 strain develop X-zones containing only non-vacuolated cells. The X-zone vacuolation is a physiologic process associated with the X-zone degeneration and is tightly regulated by genetic factors. Identification of the genetic factors controlling such strain differences should help analyze the X-zone function. In this study, a quantitative trait locus (QTL) analysis for the extent of X-zone vacuolation was performed for two types of F2 female mice: F2Ay mice (F2 mice with the Ay allele) and F2 non-Ay mice (F2 mice without the Ay allele). These were produced by crossing B6 females and DDD.Cg-Ay males. DDD.Cg-Ay is a congenic mouse strain for the Ay allele at the agouti locus and is used for this study because a close association between the X-zone morphology and the agouti locus genotype has been suggested. The Ay allele is dominant and homozygous lethal; therefore, living Ay mice are invariably heterozygotes.
Single QTL scans identified significant QTLs on chromosomes 1, 2, 6, and X for F2 non-Ay mice, and on chromosomes 2, 6, and 12 for F2Ay mice. The QTL on chromosome 2 was considered to be because of the agouti locus, which has been suggested to be associated with X-zone vacuolation. A significant QTL that interacted with the agouti locus was identified on chromosome 8.
The extent of X-zone vacuolation in DDD females was controlled by multiple genes with complex interactions. The murine X-zone is considered analogous structure to the human fetal zone. Therefore, the results of this study will aid in understanding function of not only of the X-zone but also of the human fetal zone. Identifying the genes responsible for the QTLs will be essential for understanding the molecular basis of X-zone function, which is currently unclear.
The mammalian adrenal cortex consists of three separate layers: zona glomerulosa, zona fasciculate, and zona reticularis. These layers have distinct endocrine roles. In rodents, an additional fourth, transient zone is present between the adrenal cortex and the adrenal medulla. In 1924, Masui and Tamura first discovered a presence of a large transient zone at the innermost region of the adrenal cortex that could not be found anywhere else in the adult male cortex. This zone was later named the X-zone by Howard-Miller. A close relationship was observed between X-zone morphology and gonadal functions. For example, the X-zone degenerates at puberty in males and at the first pregnancy in females.
There are apparent sex and strain differences in the morphology of the X-zone. With regard to sex difference, X-zone degeneration occurs earlier in males than in females; the X-zone disappears before 5 weeks of age in males, but gradually decreases in thickness with age in virgin females. With regard to strain differences, inbred mouse strains can be classified into two categories based on the incidence and size of X-zones and the timing of X-zone vacuolation.
Nulliparous females of the inbred mouse DDD strain have thicker X-zones than the C57BL/6J females. In DDD females, the X-zone degenerates with the accumulation of lipids; hereafter, this state is called a “vacuolated X-zone” after the designation given by Tanaka and Matsuzawa. In contrast, in C57BL/6J females, the X-zone degenerates without the accumulation of lipids; hereafter, referred to as a “non-vacuolated X-zone” Strain differences are also observed with regard to the timing of X-zone degeneration. For example, fatty degeneration of the X-zone takes place earlier in A/Cam than in CBA/FaCam females.
Such clear sex and strain differences in the X-zone appearance suggest that the morphology of this zone is controlled both hormonally and genetically. Indeed, Shire and Spickett reported that strain differences were a consequence of genetic variations at a single locus, “earlier X-zone degeneration locus” (Ex), on chromosome 7. Tanaka et al.[5, 6] reported a close association between X-zone morphology and the agouti locus genotype on chromosome 2. They suggested that the a allele suppressed the vacuolation of the cells in the X-zone in a dominant manner. While such investigations have been useful, we propose that a genome-wide study would be a more beneficial approach.
Unfortunately, only one study has attempted a genome-wide search for genes controlling X-zone morphology. Di Curzio and Goldowitz recently performed a QTL analysis on adrenal gland weight and structure using BXD recombinant inbred strains, and identified multiple significant and suggestive QTLs. In particular, they identified significant QTLs for X-zone width on chromosome 10 (Mxzwdq1) and 14 (Mxzwdq2) in males.
The X-zones in DDD/Sgn females exclusively contain vacuolated cells, whereas those in C57BL/6J strain females contain only non-vacuolated cells (Figure1). This difference may be controlled genetically. Identifying the genes responsible for the differences in the extent of X-zone vacuolation could provide clues for a better understanding of the critical role of this zone. The murine X-zone and the human fetal zone are considered analogous structures. Therefore, the results of this study will aid in understanding function of not only of the X-zone but also of the human fetal zone.
We have established a novel congenic strain for the Ay allele at the agouti locus (chromosome 2) in the inbred DDD/Sgn strain: DDD.Cg-Ay. In normal mice, the agouti gene is expressed only in the skin[9, 10], and it regulates pigmentation by serving as an inverse agonist of the melanocortin 1 receptor (MC1R)[11, 12]. However, in Ay mice, the Ay allele is associated with a large deletion, causing agouti gene expression to be aberrantly controlled by the unrelated Raly gene promoter and leading to its ectopic overexpression[10, 13–15]. As a result, Ay mice have a yellow coat. This makes it possible to distinguish the Ay mice from non-Ay mice visually. In addition, the Ay allele is homozygous lethal; therefore living Ay mice are invariably heterozygotes. DDD.Cg-Ay strain was used for this study because a close association between the X-zone morphology and the agouti locus genotype has been suggested[5, 6]. While Tanaka et al.[5, 6] investigated the effect of the a, A, and Aw alleles on the X-zone vacuolation, they did not investigate the effect of the Ay allele. Comparison of X-zone morphology between B6 and B6.Cg-Ay, and DDD and DDD.Cg-Ay makes it possible to reveal the effect of the Ay allele. Furthermore, use of DDD.Cg-Ay strain together with C57BL/6J strain makes it possible to include the effect of the Ay allele in combination with the a and A alleles in the QTL analyses in F2 mice. The objectives of this study were to determine the genetic basis for strain differences in the extent of X-zone vacuolation between the DDD/Sgn and C57BL/6J strains and to clarify a possible effect of the agouti locus genotype on X-zone vacuolation.
The inbred mouse DDD/Sgn strain (hereafter designated DDD, coat color genotype is AABBcc) and the congenic mouse DDD.Cg-Ay strain (hereafter designated DDD-Ay, AyABBCC) were maintained at the National Institute of Agrobiological Sciences (NIAS). The inbred mouse C57BL/6J strain (hereafter designated B6, aaBBCC) was purchased from Clea Japan (Clea Japan, Inc., Tokyo, Japan). The congenic mouse B6.Cg-Ay strain (hereafter B6-Ay, AyaBBCC) was purchased from The Jackson Laboratory (Bar Harbor, ME, USA). The DDD-Ay strain was established by introgressing the Ay allele from the B6-Ay strain in the DDD strain by backcrossing for 12 generations. Hereafter, both DDD-Ay and B6-Ay are referred to as “Ay mice” Similarly, their control littermates, DDD and B6, are both referred to as “non-Ay mice” The Ay allele at the agouti locus (chromosome 2) is dominant and homozygous lethal; therefore, living Ay mice are invariably heterozygotes. Ay mice can be distinguished visually by their yellow coat color from non-Ay mice.
DDD-Ay males were crossed with B6 females to produce the F1 generation, and F1Ay (AyaBBCC) mice were intercrossed with F1 non-Ay (AaBBCC) mice to produce the F2 generation. F2 females were weaned at 4 weeks. The mice were housed in groups of 4–5 for 16 weeks.
All mice were maintained in a specific-pathogen-free facility with a regular light–dark cycle (12 h light and 12 h dark) and controlled temperature (23 ± 1°C) and humidity (50%). Food (CRF-1; Oriental Yeast Co., Ltd., Tokyo, Japan) and water were freely available throughout the experimental period. All animal experiments were performed in accordance with the guidelines of the Institutional Animal Care and Use Committee of NIAS.
At the age of 16 weeks, mice were euthanized with an overdose of ether and their adrenal glands were removed. Formalin-fixed tissues were embedded in paraffin, sectioned, and stained with hematoxylin and eosin.
The extent of X-zone vacuolation was evaluated semi-quantitatively or qualitatively. The width of the vacuolated layer of the X-zone could not be determined by a direct measurement because either the adrenal gland was not completely round, the X-zone was not always concentric, or a section was not necessarily made from the very center of the organ. According to Janat and Shire, CXB recombinant inbred strain mice can be divided into four types, including two parental types, based on X-zone morphology. Thus, the degree of X-zone vacuolation was evaluated quantitatively according to the following four-grade system (Figure2A).
“Grade 0” indicates that the X-zone contains only non-vacuolated cells; this corresponds to X-zone morphology in the parental B6 (−Ay) strain. The layer of vacuolated cells in an X-zone of “Grade 3” is the thickest among the grades; this corresponds to X-zone morphology in the parental DDD (−Ay) strain. The layer of vacuolated cells in an X-zone of “Grade 1” and “Grade 2” is thinner than that of “Grade 3” The layer of vacuolated cells in an X-zone of “Grade 2” is apparently thicker than that in an X-zone of “Grade 1”.
Alternatively, the occurrence of a vacuolated X-zone was evaluated qualitatively by regarding this as a binary trait. That is, an X-zone of “Grade 0” as indicated above was recognized as containing non-vacuolated cells only and X-zones of “Grades 1–3” were recognized as containing vacuolated cells.
In this study, the grade of X-zone vacuolation was treated in three different ways: as a parametric trait, as a non-parametric trait, and as a binary trait. QTLs that were identified as significant in at least one of these three analyses were considered to be significant.
Genotyping and QTL analysis
Genomic DNA was isolated from the tails of mice using a commercial DNA extraction kit (Wizard Genomic DNA Purification Kit; Promega, Madison, WI, USA). Microsatellite sequence length polymorphisms were identified after PCR amplification of genomic DNA. PCR products were separated by 10% polyacrylamide gel electrophoresis and visualized with ethidium bromide straining.
Mice were genotyped for the following microsatellite marker loci: D1Mit231, D1Mit303, D1Mit10, D1Mit102, D1Mit16, Apoa2 (see below), D1Mit291, D2Mit312, D2Mit296, D2Mit92, D2Mit304, D2Mit285, D2Mit346, D3Mit203, D3Mit25, D3Mit212, D4Mit1, D4Mit178, D4Mit166, D4Mit234, D5Mit267, D5Mit113, D5Mit239, D5Mit161, D5Mit221, D6Mit116, D6Mit224, D6Mit188, D6Mit39, D6Mit108, D6Mit256, D6Mit259, D7Mit250, D7Mit362, D8Mit191, D8Mit205, D8Mit249, D8Mit183, D9Mit59, D9Mit191, D9Mit207, D9Mit198, D9Mit212, D10Mit188, D10Mit183, D10Mit42, D10Mit95, D11Mit236, D11Mit36, D11Mit124, D11Mit61, D12Mit136, D12Mit172, D12Mit156, D12Mit259, D12Mit141, D12Nds2, D13Mit207, D13Mit64, D13Mit110, D13Mit213, D13Mit171, D14Mit64, D14Mit193, D14Mit165, D15Mit174, D15Mit184, D15Mit193, D16Mit131, D16Mit57, D16Mit136, D16Mit139, D16Mit49, D17Mit164, D17Mit176, D17Mit139, D17Mit93, D17Mit123, D18Mit21, D18Mit149, D18Mit152, D18Mit25, D19Mit32, D19Mit91, D19Mit35, DXMit166, DXMit119, DXMit64, and DXMit38. Apoa2 (apolipoprotein A-II) was genotyped with a PCR-RFLP method according to the Suto et al. procedure.
It should be noted that the chromosome 7 is divided into two parts. As a consequence of the introgression of the Tyr locus from the B6 strain, a mid-part of the DDD genome on chromosome 7 is replaced by a B6 genome in DDD-Ay mice. In this study, a region proximal to the B6 region was defined as “chromosome 7.1 (D7Mit250)” while a region distal to the B6 region was defined as “chromosome 7.2 (D7Mit362)”.
Of a total of 298 F2 females, 148 were F2 non-Ay and 150 were F2Ay mice. QTL analysis was done using R/qtl[19, 20]. First, F2Ay and F2 non-Ay mice were analyzed independently. Threshold LOD scores for suggestive (P < 0.63) and significant (P < 0.05) linkages were determined by performing 1,000 permutations for each trait. For significant QTLs, a 95% confidence interval (CI) was defined by a decline of 1.5-LOD. After these single QTL scans, pair-wise evaluations for potential interactions between loci were made. At this stage, threshold LOD scores were based strictly on those recommended by Broman in “A brief tour of R/qtl” (http://www.rqtl.org). Next, data for F2 non-Ay and F2Ay mice were combined and reanalyzed. The calculations for the threshold LOD scores were repeated. The presence or absence of possible statistical interactions between the genotypes at QTLs and the agouti locus (non-Ay and Ay) was evaluated by two-way ANOVA.
The combined effects of all QTLs, including those that were significant and suggestive, were assessed using multiple QTL models. The percent of the variance explained by each QTL was reported based on these models.
Statistical analysis between two groups was performed using the Student’s or Welch’s t-test, or the Wilcoxon or Kruskal-Wallis test. Statistical analysis between more than two groups was performed using Tukey’s multiple comparisons tests with JMP8 software (SAS Institute Japan, Tokyo, Japan). P <0.05 was considered to be statistically significant.
Comparisons of X-zone morphologies among the DDD-Ay, DDD, B6-Ay, and B6 strains
At the age of 16 weeks, X-zone morphologies in both sexes were compared among the DDD-Ay, DDD, B6-Ay, and B6 strains. Comparison of X-zone morphology between B6 and B6.Cg-Ay, and DDD and DDD.Cg-Ay makes it possible to reveal the effect of the Ay allele. In agreement with previous findings, the X-zone was absent in males, irrespective of strain or agouti locus genotype (Figure1A). Females had X-zones and as expected, there were gross strain differences in the extent of vacuolation. DDD-Ay and DDD females had X-zones that contained exclusively vacuolated cells, whereas B6-Ay and B6 females had X-zones containing only non-vacuolated cells (Figure1B). X-zone vacuolation in all DDD-Ay (n = 4) and DDD (n = 2) females was scored as grade 3 (Figure2A). In contrast, X-zone vacuolation in all B6-Ay (n = 4) and B6 (n = 2) females was scored as grade 0.
X-zone vacuolation in F1 and F2 mice
X-zone vacuolation was also evaluated in (♀B6 × ♂DDD-Ay) F1 and F2 mice. Because the agouti locus genotype of B6 strain was a/a and that of DDD-Ay strain was Ay/A, the agouti locus genotype of F1 mice was either A/a (F1 non-Ay mice) or Ay/a (F1Ay mice). In the similar way, F2 non-Ay mice had either A/a or a/a genotype and F2Ay mice had either Ay/a or Ay/A genotype (See also Materials and methods). All F1 non-Ay (n = 5) and all F1Ay (n = 5) mice had vacuolated X-zones of grade 1 or 2; the average grade was 1.6 in both F1 types.
Histograms showing these grade distributions in F2 non-Ay (n = 148) and F2Ay (n = 150) mice are shown in Figure2B. The mean ± S.E. grades in F2 non-Ay and F2Ay mice were 1.92 ± 0.09 and 2.05 ± 0.09, respectively. There was no significant difference between these two F2 types. When the grade was treated as a binary trait, the number of mice with grade 0 (absence of vacuolation) was 16 (10.8%) in F2 non-Ay and 24 (16.0%) in F2Ay mice.
We first performed single QTL scans. When the grade was analyzed as a parametric trait in F2 non-Ay mice, three significant QTLs were identified on chromosomes 1, 2, and X. These loci were named Xzvdq1 (X-zone vacuolation in DDD mice QTL no. 1), Xzvdq2, and Xzvdq3, respectively (Table1 and Figure3A). The DDD allele was associated with higher grades of vacuolation at Xzvdq1 and Xzvdq2, whereas the DDD allele was associated with a lower grade of vacuolation at Xzvdq3 (Figure4A–C). When the grade was analyzed as a non-parametric trait, one significant QTL was newly identified on chromosome 6; this locus was named Xzvdq4. The DDD allele was associated with a higher grade of vacuolation at Xzvdq4 (Figure4D). When the grade was analyzed as a binary trait, Xzvdq3 on X chromosome was the only significant QTL.
When the grade was analyzed as a parametric trait in F2Ay mice, two significant QTLs were identified on chromosomes 6 and 12. These loci were named Xzvdq4 and Xzvdq5, respectively, because the former locus was located at a position similar to that identified in F2 non-Ay mice (Table2 and Figure3A, B). The DDD allele was associated with a higher grade of vacuolation at Xzvdq4, whereas the DDD allele was associated with a lower grade of vacuolation at Xzvdq5 (Figure5E, F). When the grade was analyzed as a non-parametric trait, one significant QTL was newly identified on chromosome 2. This locus was named Xzvdq2 because this locus was located at a position similar to that identified in F2 non-Ay mice (Table2 and Figure3A, B). The DDD allele was associated with a higher grade of vacuolation at Xzvdq2 (Figure5G). Xzvdq4 was the only significant QTL when the grade was analyzed as a binary trait.
Next, we combined the Ay and non-Ay progeny of the same F2 cross and performed single QTL scans. When the grade was analyzed as either a parametric or non-parametric trait, significant QTLs were identified on chromosomes 1, 2, and 6 (Table3 and Figure3C). Xzvdq3 on chromosome X was no longer identified, even as a suggestive QTL. No significant QTLs were identified when the grade was analyzed as a binary trait. Additional analyses were done by using the agouti locus genotype as a covariate because the results of single QTL scans substantially differed between the two F2 types. Because the F2 non-Ay mice had A/a or a/a genotypes and the F2Ay mice had Ay/A or Ay/a genotypes at their agouti locus, these four genotypes were distinguished and included as covariates.
The agouti locus genotype was estimated by genotyping the genetic marker nearest to the agouti locus. The agouti locus is located at 76.83 cM (154.6 Mbp); therefore, D2Mit285, which is located at 75.41 cM (152.6 Mbp), was used for agouti locus genotyping. When the agouti locus genotype was included as an additive covariate, no additional QTLs were identified (Table4). When the agouti locus genotype was included as an interactive covariate, one additional significant QTL was identified on chromosome 8; this locus was named Xzvdq6.
Because the difference between the LOD score with the agouti locus genotype as an interactive covariate and the LOD score with the agouti locus genotype as an additive covariate concerns the test of the QTL × agouti locus genotype interaction, this test was done for combined F2 mice. One significant QTL was identified on chromosome 8 (Figure6, LOD scores plotted as solid lines). The effects of interaction between agouti (D2Mit285) and Xzvdq6 (D8Mit191) are shown in Figure7A. Next, the agouti genotypes were classified into two categories: presence or absence of the Ay allele. Results of this analysis were very similar to those obtained above (Figure6, LOD scores plotted as dashed lines). The effects of interaction between agouti (D2Mit285) and Xzvdq6 (D8Mit191) are shown in Figure7B.
Next, possible interactions were analyzed pair-wise for F2 non-Ay and F2Ay mice. No significant pair-wise interactions were identified.
Finally, the relative contributions of each QTL when considered together were evaluated using multiple QTL models (Table5). Most of the QTLs identified in the previous analyses were confirmed by this analysis. It should be noted that the LOD score for a locus on chromosome 8 in combined F2 mice increased to 4.85 when considering the simultaneous effects of other QTLs. The proportions of the total phenotypic variance accounted for in the F2 non-Ay, F2Ay, and combined F2 mice were 42.9%, 32.6%, and 34.8%, respectively.
The suggestive effect of the agouti locus genotype
As mentioned previously, a significant QTL, Xzvdq2, was identified on distal chromosome 2. There was a possibility that Xzvdq2 was suggested to be due to agouti because some studies have suggested that the agouti locus was likely to have an effect on X-zone vacuolation[5, 6]. In F2 non-Ay mice, those with the A/a genotype had a significantly higher grade of vacuolation compared with mice having a/a genotype based on the four-grade evaluation (Table6). However, based on the all or none evaluation (i.e., binary 1 or 0), there was no significant difference between the two genotypes. In F2Ay mice, those with the Ay/A genotype had a significantly higher grade of vacuolation than did mice with the Ay/a genotype. Again, based on the all or none evaluation, no significant difference was identified between the two genotypes.
Multigenic basis responsible for X-zone vacuolation
The extent of X-zone vacuolation in F1 mice was intermediate compared with the parental strains, and that in F2 mice was varied. Therefore, the extent of X-zone vacuolation is suggested to be a quantitative phenotype that is determined by multiple genes. Indeed, results of our QTL analyses revealed a multigenic basis for X-zone vacuolation.
Among the identified QTLs, Xzvdq2 and Xzvdq4 on chromosomes 2 and 6, respectively, were identified in both F2 types; the LOD scores for these QTLs increased in the combined F2 mice. Therefore, these QTLs were not disturbed by the Ay allele. In contrast, Xzvdq1, Xzvdq3, and Xzvdq5 on chromosomes 1, X, and 12, respectively, showed high F2-type specificity (Tables1,2, and3 and Figure3A–C). In particular, Xzvdq3 was not identified, even as a suggestive QTL, in combined F2 mice. Therefore, it was expected that the Xzvdq3 would interact with the agouti genotype.
The interaction LOD score for Xzvdq3 was certainly high, but was below the significant threshold (Figure6). This suggests that the effect of Xzvdq3 is in same direction in both F2 non-Ay and F2Ay mice, but is substantially weaker in the presence of the Ay allele. Intriguingly, the B6 allele at Xzvdq3 on X chromosome was associated with a higher grade of vacuolation not only in the parametric analysis for F2 non-Ay mice, but also in the binary analysis. This indicates that the B6 allele exerts its effect more strongly than does the DDD allele for determining whether or not X-zone vacuolation develops.
Overall, four significant QTLs were identified for F2 non-Ay mice and three significant QTLs were identified for F2Ay mice. With regard to the number of QTLs responsible for X-zone vacuolation, Tanaka et al. estimated that there would be three loci based on their study of SMXA recombinant inbred strains. The present results are in agreement with this estimation.
The suggestive effect of the agouti locus genotype on the X-zone vacuolation
A putative genetic link between the agouti locus genotype and X-zone vacuolation was suggested by Tanaka et al.[5, 6]. In the SM/J strain background at 70 days, mice with the Aw/Aw genotype had X-zones containing highly vacuolated cells, whereas mice with the Aw/a or a/a genotypes had X-zones containing only non-vacuolated cells. These results suggested the a allele suppressed X-zone vacuolation in a dominant manner.
In the BALB/c strain background at 70 days, mice with the A/A genotype had X-zones containing highly vacuolated cells, whereas BALB/c strain mice with the a/a genotype (coisogenic mutant occurring in the BALB/c strain) had X-zones containing only non-vacuolated cells. However, at 140 days, BALB/c mice with both the A/A and a/a genotypes had X-zones containing only vacuolated cells. These results suggested that the a allele was not only involved with the extent of X-zone vacuolation, but also with the timing of X-zone degeneration. It should be noted that B6 females never develop X-zone vacuolation regardless of age, which is in contrast to a BALB/c background.
In this study, the F2 non-Ay mice had A/a and a/a genotypes; the former was heterozygous and the latter was homozygous for the B6 allele. Similarly, the F2Ay mice had Ay/A and Ay/a genotypes; the former was homozygous and the latter was heterozygous for the DDD allele. When the vacuolation grade was analyzed as a parametric or non-parametric trait, significant differences were observed between the two genotypes in both F2 types (Table6). The difference between genotypes was larger in F2 non-Ay mice than in F2Ay mice. In contrast to the Tanaka et al. proposal, the a allele suppressed vacuolation in a semidominant manner.
In this regard, it was also possible that the A allele promoted vacuolation. Thus, differences between the Ay/A and Ay/a alleles in F2Ay mice was not as strong as that between the A/a and a/a alleles in F2 non-Ay mice. In contrast, when the vacuolation grade was analyzed as a binary trait, the effect of the a allele was not significant in both F2 types. These results suggest that the agouti locus may have different genetic effects depending on different genetic background.
When the agouti locus genotypes were included as covariates by distinguishing four genotypes (Ay/A, Ay/a, A/a, and a/a), Xzvdq6 was identified on chromosome 8 as an interaction locus. When the agouti locus genotypes were included as covariates by distinguishing two genotypes (Ay or non-Ay), Xzvdq6 was again identified. The patterns of LOD score plots were very similar for these two analyses. Therefore, whether or not mice had the Ay allele was critically important for the interaction with Xzvdq6 on chromosome 8. This interaction may be one of the factors causing differences in the results in the aforementioned single QTL scans between F2 non-Ay and F2Ay mice.
These points of discussion are based on the assumption that Xzvdq2 is due to the agouti locus. However, the possibility that Xzvdq2 is due to another locus near to the agouti locus cannot be ruled out. Indeed, the agouti locus spans 259 kb on distal chromosome 2, and this region contains three other protein coding genes (Raly, Eif2s2, and Gm14226).
Candidate genes or loci
Shire and Spickett reported the presence of an “earlier X-zone degeneration locus” (Ex), on chromosome 7. The Ex locus is involved with the timing of X-zone degeneration rather than the extent of X-zone vacuolation; therefore, Ex is irrelevant to this study because the B6 strain never develops X-zone vacuolation regardless of mouse age[3, 17, 22]. The genomic region surrounding Tyr locus on chromosome 7 in DDD-Ay mice has been replaced by the B6 genome; DDD-Ay mice had X-zones containing vacuolated cells in a manner similar to DDD mice.
Janat and Shire reported the presence of two gene loci that controlled X-zone development on chromosomes 12 (Exz2) and 16 (Exz1) in CXB recombinant inbred strains, which were derived from C57BL/6By and BALB/cBy strains. Inferring from their linkage analysis, Exz2 may be located on distal chromosome 12; therefore, it may be allelic with the Xzvdq5.
Di Curzio and Goldowitz addressed adrenal gland structure by QTL analysis. They analyzed X-zone widths in BXD recombinant inbred strains derived from the strains B6 and DBA/2J. They failed to identify any QTLs in females, but identified significant QTLs for X-zone width on chromosome 10 (Mxzwdq1) and 14 (Mxzwdq2) in males. Both of these QTLs did not coincide with those identified in this study.
Based on information retrieved from Mouse Genome Informatics, only a few genes or loci are currently recognized as having effects on the X-zone morphology. A possible candidate gene for Xzvdq1 on chromosome 1 is KiSS-1 metastasis-suppressor (Kiss1). Nuclear receptor subfamily 0, group B, member 1 (Nr0b1, also known as Dax1) was also a possible candidate gene for Xzvdq3 on the X chromosome. In particular, Nr0b1 was cloned as the gene responsible for X-linked congenital adrenal hypoplasia in humans[25, 26]. Interestingly, loss of the function of Nr0b1 gene in humans and mice results in the lack of degeneration of the fetal zone and X-zone, respectively[24–26]. For these reasons, the fetal zone and X-zone are considered analogous structures.
Because Xzvdq6 interacts with an agouti genotype and is located on chromosome 8, the melanocortin 1 receptor (Mc1r) gene may be a possible candidate gene. Mc1r is located at the distal part of this chromosome (72.1 cM); therefore, Xzvdq6 is unlikely to be allelic with Mc1r because 95% CI for Xzvdq6 ranges from 21 to 34 cM. Adrenocortical dysplasia (Acd), which suppresses X-zone development, is also known to be located on chromosome 8. The Acd locus is at 53.04 cM on this chromosome and, therefore, is unlikely to be allelic with Xzvdq6.
X-zone morphology, including the extent of vacuolation, is determined genetically and, at the same time, modified hormonally. Regarding hormonal factors, without doubt testosterone is critically important. Testosterone administration induces X-zone degeneration, whereas gonadectomy preserves the X-zone in both sexes[28, 29]. However, the X-zone degenerates in testicular feminized male (ArTfm/Y) mice, suggesting that androgen is not necessarily required for X-zone degeneration. Nevertheless, androgen is still a critical factor for X-zone degeneration; therefore, genes that are controlled by androgen are possible candidate genes for the identified QTLs.
Despite efforts to elucidate critical roles of the X-zone, the physiological significance of this zone remains uncertain. Thus, it is most important to identify genes that account for the variations observed in X-zone morphology. Simultaneously, this study addressed the extent of X-zone vacuolation by adopting a genome-wide scan approach and showed that the extent of X-zone vacuolation in DDD females was controlled by multiple genes with complex interactions. The murine X-zone and the human fetal zone are considered analogous structures. Therefore, the results of this study will aid in understanding function of not only of the X-zone but also of the human fetal zone. In addition, there is need to identify additional QTLs because there have been a limited number of genetic studies on adrenocortical morphology, including X-zone vacuolation. Identifying the genes responsible for the QTLs will be essential for understanding the molecular basis of X-zone function.
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This work was funded in part by an institutional grant. Microsatellite genotyping, most of which had been performed for our previous studies using the same mice, was funded in part by a grant from Kieikai Research Foundation.
The author declares that he has no competing interests.
JS has designed the research, carried out experiments for data collection, analyzed the data, and written the manuscript. The author read and approved the final manuscript.
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Suto, J. Quantitative trait locus mapping of genes associated with vacuolation in the adrenal X-zone of the DDD/Sgn inbred mouse. BMC Genet 13, 95 (2012) doi:10.1186/1471-2156-13-95
- Adrenal X-zone
- DDD mice
- Quantitative trait locus (QTL) mapping