The frequency of the Robertsonian (ROB) translocation in newborn babies is approximately one in 1000 [1]. The ROB translocation is an unusual type of chromosome rearrangement caused by two particular chromosomes joining together. In humans, it occurs in the five acrocentric chromosomes, such as chromosomes 13, 14 and 15 (group D), and 21 and 22 (group G). During a ROB translocation, the participating chromosomes break at their centromeres and the long arms fuse to form a single chromosome with a single centromere. The short arms also join to form a reciprocal products that typically contain nonessential genes and are usually lost within a few cell divisions. The most common ROB translocation in humans is between chromosomes 13 and 14, constituting 75.0% of all ROB translocations [1]. Since ROB translocation carriers have a balanced chromosomal complement, they may never be aware of their unusual chromosome rearrangement. Therefore, ROB translocation can be passed down in the family for many generations without detection.
In ROB translocations, at the end of meiosis I, segregation of the translocated and non translocated chromosomes from the two different implicated chromosome pairs, lead to the formation of either balanced (alternate segregation mode) or unbalanced (adjacent 1, adjacent 2, and 3:0 segregation modes) gametes that can segregate in different ways at anaphase [2,3]. Only alternate segregation produces normal/balanced karyotypes. The other segregation modes (adjacent 1, adjacent 2, 3:0) produce unbalanced gametes with disomies and nullisomies of chromosomes involved in ROB translocations. It is well-known that meiotic tetravalent configuration tends to segregate in an alternate way [4], resulting in the production of normal/balanced spermatozoa. However, a certain percentage of unbalanced gametes deriving from adjacent segregation are also produced, and could be responsible for the miscarried or the severely affected aneuploidy offspring frequently born to these carriers.
Analysis of the chromosomal constitution in sperm of ROB translocation carriers is of great interest to assess the risk of unbalanced offspring for genetic counseling. Sperm fluorescence
More recently, inter-chromosomal effects (ICE) have been reported in several chromosome pairs in ROB translocations. Inter-chromosomal effects refer to a disturbance of meiosis, where rearranged chromosomes disrupt dis-junction and distribution of chromosome pairs not involved in the rearrangement. The concept of ICE was first postulated by Lejeune [11], who noticed an excess of carriers of balanced reciprocal translocations among the fathers of children with Down syndrome. Since then, contradictory data have been reported in ROB translocation carriers. Several studies have found such an ICE in male carriers of ROB translocations [12,13], but others did not [14,15]. The aims of this study were to analyze the segregation pattern of ROB translocation in 13 male carriers, and evaluate the occurrence of ICE on chromosomes 18, X and Y in these carriers.
Thirteen male carriers of ROB translocations (designated P1-13) consulting for infertility or repeated abortions were included in this study. Twelve were heterozygous ROB translocation and one was a homozygous ROB translocation. Except P1 and P2 (P2 was P1’s father), all the patients were unrelated. Three males with normal 46, XY karyotype and normal sperm characteristics were recruited as controls. The local ethics committee approved this protocol and all patients and controls had previously given informed consent for the study.
All semen samples were first analyzed to evaluate volume, concentration and motility according to the World Health Organization (WHO) criteria [16]. After semen analysis, sperm with progressive motility was isolated and washed twice in phosphate buffered saline (pH 7.4) by centrifugation at 1500 rpm for 11 min. Final pellets were fixed with 5 mL of acetic acid/methanol mixture (1:3) for at least 30 min. at 4 °C. Aliquots (40-50 μL) of the resulting suspension of nuclei were smeared on cold pre-cleaned slides. Nuclei decondensation was performed in 1 N NaOH for 2 min. After dehydration in ethanol series (70.0, 90.0, 100.0%), denaturation was performed in 0.25% formamide in 2 × saline sodium citrate (SSC) followed by overnight hybridization with a combination of commercially available probes.
To assess the segregation behavior of each rearrangement, a dual-color FISH using locus-specific probes and/or telomere probes and/or chromosome enumeration probes, was carried out on spermatozoa of the translocation carriers. Below we list the probes that we used to identify the segregation products for each karyotype. For a der(13;14) carrier, LSI13 (13q14, Spectrum Green) and Tel14 (14q32.33, Spectrum Red) were used. For a der(14;15) carrier, Tel14 (14q32.33, Spectrum Red) and Tel15 (15q26.3, Spectrum Green) were used. For a der(14;21) carrier, Tel14 (14q32.33, Spectrum Red) and LSI21 (21q22.13-q22.2, Spectrum Green) were used. For a der(13;22) carrier, LSI13 (13q14, Spectrum Green) and LSI22 (22q12.3, Spectrum Red) were used. For a der(21;22) carrier, LSI21 (21q22.13-q22.2, Spectrum Green) and LSI22 (22q12.3, Spectrum Red) were used. Regarding ICE evaluation, triple-color FISH was performed using the probe mixture including commercial satellite (DNA) probes for chromosomes 18, X and Y (CEP 18, Spectrum Blue/CEP X, Spectrum Green/CEP Y, Spectrum Red) from Vysis (Abbott Park, IL, USA).
Post-hybridization washes included 2 min. in 0.4 × SSC/0.3% NP-40 (pH 7) at 72 °C, followed by 1 min. in 2 × SSC/0.1% NP-40 (pH 7) at room temperature. Slides were covered with DAPI II (Vysis). Only intact spermatozoa bearing a similar degree of decondensation and clear hybridization signals were scored. Disrupted or overlapping spermatozoa were excluded from analysis. Only slides with hybridization efficiency of 99.0% and more were analyzed. One thousand sperm nuclei per patient were analyzed.
The χ2 test was used to compare the frequencies of segregation products. A
The age of our patients ranged from 25 to 48 years with a mean of 38.6 years. The karyotype and sperm examination of patients and controls are given in Table 1. According to WHO criteria, all our patients, except P1, had very poor semen parameters. The karyotyping analysis identified a previously undescribed balanced human karyotype 44, XY, der(14;15)(q10;q10), der(14;15)(q10;q10) (Figure 1). Interestingly, in P1, we saw a sperm (arrow) with four fluorescence signals (two red and two green). This means the sperm has two derivative chromosomes of der(14;15), but we could not tell if the sperm was a disomy of derivative chromosome or diploid (Figure 2). In future studies, we will employ triple-color FISH (for example, the probe mixture will consist of chromosomes 14, 15 and 18) for the detection of normal/balanced or unbalanced sperm to distinguish between disomy and diploid.
Cytogenetic and spermiologic results of patients and controls. Sperm motility was graded from a to d, according to the WHO manual criteria, as follows. Grade a (fast progressive) sperms are those that swim forward fast in a straight line, like guided missiles. Grade b (slow progressive) sperms swim forward, but either in a curved or crooked line, or slowly (slow linear or non linear motility). Grade c (non progressive) sperms move their tails, but do not move forward (local motility only). Grade d (immotile) sperms do not move at all. The (a+b)% represent the percentage of sperm that can move forward normally.
Patient
Karyotype
Age (years)
Sperm Concentration (106/L)
Motility
P1
44, XY, der(14;15)(q10;q10), der(14;15)(q10;q10)
25
56.0
53.0
P2
45, XY, der(14;15)(q10;q10)
48
13.0
22.0
P3
45, XY, der(13;14)(q10;q10)
29
19.0
25.0
P4
45, XY, der(13;14)(q10;q10)
31
22.0
17.0
P5
45, XY, der(13;14)(q10;q10)
27
38.0
21.0
P6
45, XY, der(13;14)(q10;q10)
35
57.0
59.0
P7
45, XY, der(13;14)(q10;q10)
33
89.0
38.0
P8
45, XY, der(13;14)(q10;q10)
30
35.0
29.0
P9
45, XY, der(14;21)(q10;q10)
36
40.0
35.0
P10
45, XY, der(14;21)(q10;q10)
32
37.0
36.0
P11
45, XY, der(14;21)(q10;q10)
26
42.0
45.0
P12
45, XY, der(13;22)(q10;q10)
26
28.0
39.0
P13
45, XY, der(21;22)(q10;q10)
29
31.0
47.0
C1
46, XY
35
77.0
44.0
C2
46, XY
27
62.0
47.0
C3
46, XY
33
43.0
39.0
The results of the segregation analysis are given in Table 2 and Table 3. Among the 13 ROB translocation carriers, one was homozygous (P1). The remainder were heterozygous (P2-P13). The frequency of balanced spermatozoa was 99.7% in P1, while the frequency of unbalanced spermatozoa was 0.3%, which was similar to the controls [17-21] (Table 2).
The number of spermatozoa scored, the alternate mode of segregation, incidence of sperm nullisomy, disomy and 3:0/diploid for the chromosomes involved in the Robertsonian translocation in 13 Robertsonian translocation carriers and three controls. A: first chromosome involved in the ROB translocation; B: second chromosome involved in the ROB translocation; D/D mean: the mean of P2-P8 (ROB translocation between D/D groups); D/G mean: the mean of P9-P12 (ROB translocation between D/G groups); Control mean: the mean of the three controls (C1-C3).
Normal/Balanced
Nullisomy A
Disomy A
Nullisomy B
Disomy B
3:0 or Diploid
Unbalanced
Total
P1
997
2
0
0
0
1
3
1000
P2
799
41
49
55
45
11
201
1000
P3
852
24
57
34
26
7
148
1000
P4
809
68
30
55
29
9
191
1000
P5
843
40
39
27
41
10
157
1000
P6
757
55
37
94
42
15
243
1000
P7
837
29
66
34
21
13
163
1000
P8
782
75
61
49
22
11
218
1000
D/D mean
811
47.0
48.0
50.0
32.0
11.0
189.0
P9
775
41
50
70
45
19
225
1000
P10
721
66
37
110
45
21
279
1000
P11
704
47
56
73
95
25
296
1000
P12
719
69
75
62
58
17
281
1000
D/G mean
730
56.0
55.0
79.0
61.0
21.0
270.0
P13
768
47
51
42
80
12
232
1000
C1
995
0
2
1
1
1
5
1000
C2
997
1
0
2
0
0
3
1000
C3
995
0
2
0
1
2
5
1000
Control mean
996
0.3
1.3
1.0
0.7
1.0
4.3
Incidence of sperm nullisomy, disomy and diploid for chromosomes 18, X and Y in 13 Robertsonian translocation carriers and three controls.
Normal/Balanced
Nullisomy 18
Disomy 18
Nullisomy Sex Chromosome
Disomy Sex Chromosome
3:0 or Diploid
Unbalanced
Total
P1
994
0
1
2
3
0
6
1000
P2
949
3
2
15
10
21
41
1000
P3
899
6
5
22
21
47
101
1000
P4
952
4
5
17
12
10
48
1000
P5
913
11
9
13
15
39
87
1000
P6
947
7
2
15
17
12
53
1000
P7
955
9
12
10
5
9
45
1000
P8
901
21
13
24
19
22
99
1000
D/D mean
931
8.7
6.9
16.6
14.1
22.9
67.7
P9
976
3
4
4
2
11
24
1000
P10
985
2
1
3
6
3
15
1000
P11
963
6
4
9
11
7
37
1000
P12
944
7
5
8
11
25
56
1000
D/G mean
967
4.5
3.5
6.0
7.5
11.5
33.0
P13
977
7
6
1
4
5
23
1000
C1
995
0
2
1
1
1
5
1000
C2
997
1
0
2
0
0
3
1000
C3
991
0
2
3
1
3
9
1000
Control mean
994
0.3
1.3
2.0
0.7
1.3
5.7
In P2-P13, the frequency of normal/balanced spermatozoa resulting from alternate segregation varied between 70.4 and 85.2%. The frequency of unbalanced spermatozoa resulting from adjacent segregation varied between 14.8 and 29.6%. The frequency of unbalanced spermatozoa was significantly higher than P1 and the controls (
To evaluate the occurrence of ICE, the nullisomy, disomy and diploid frequencies for chromosomes 18, X and Y are summarized in Table 3. Increased frequencies of aneuploidy for a sex chromosome were observed in 10 ROB translocation carriers (P2-P8, P10-P12), Increased frequencies of aneuploidy for chromosome 18 were observed in 10 ROB translocation carriers (P3-P9, P11-P13). In addition, increased frequencies of diploid were found in 11 ROB translocation carriers (P2-P9, P11-P13). Increased frequencies of unbalanced sperms were found in heterozygous carriers (P2-P13). In contrast, no ICE was detected in P1.
Sperm chromatin is a highly organized, compact structure consisting of DNA and heterogeneous nucleoproteins, which are essential for the accurate transmission of genetic information to offspring [22]. Sperm FISH is most commonly used to determine the proportion of aneuploidy present in sex chromosomes and autosomes of infertile men. Furthermore, it can also quantify the probability of transmitting aneuploidies and complex chromosomal rearrangements, such as translocations and inversions [22]. As a result, sperm FISH analysis is increasingly included in infertility diagnostic protocols, providing useful information for genetic consulting. In our study, we performed sperm FISH analyses on 13 male ROB translocation carriers.
In our study, we had one homozygous carrier (P1) and 12 heterozygous carriers (P2-P13). In P1, the frequency of unbalanced spermatozoa was only 0.3% that was similar to controls and is consistent with previous publications [5-7]. In contrast, in P2-P13, the frequency of normal/balanced spermatozoa resulting from alternate segregation varied between 70.4 and 85.2% (Table 2). This is consistent with previous studies showing that alternate segregation is predominant in sperm of Robertsonian translocation carriers [11,20,21]. The high prevalence of the alternate segregation is presumably due to
The homozygous ROB translocation carrier (P1) is healthy and has a balanced chromosomal complement. Assessment of a semen sample from P1 showed normal sperm number and morphology. Given his karyotype of 44, XY, der(14;15)(q10;q10), der(14;15)(q10;q10), we hypothesized that the person’s sperm karyotype to be consistently 22, X, der(14;15)and 22, Y, der(14;15), then, our hypothesis was proven by this research. Most of the sperm from P1 are balanced haploid (not normal haploid) (Table 2, Table 3). Homozygous ROB translocations in man have been described before. A fetus with two t(14;21) chromosomes was found by Dallapiccola
Inter-chromosomal effect remains controversial in the literature [29]. Some publications have indicated its relevance [12,13], while others showed no evidence of ICE in ROB translocation carriers [9,18]. Inter-chromosomal effect could be explained by the formation of heterosynapses between chromosomes involved in the translocation and the sex vesicle, which could also involve other chromosomes [11,29]. In our study, we observed higher frequency of aneuploidy for the sex chromosome in 10 ROB translocation carriers (P2-P8, P10-P12) and higher frequencies of aneuploidy for chromosome 18 in 10 ROB translocation carriers (P3-P9, P11-P13). In addition, increased rates of diploid were found in 11 ROB translocation carriers (P2-P9, P11-P13). Increased rates of unbalanced sperms were found in all ROB translocation heterozygote (P2-P13). The incidence of spermatozoa with nullisomy, disomy and diploid for the sex chromosomes of ROB translocation heterozygotes (P2-P13) was significantly higher compared to that of ROB translocation homozygosity (P1) (
To conclude, our study confirmed that alternate segregation is dominant in ROB translocation carriers. However, despite the high number of normal/balanced spermatozoa, there are still a lot unbalanced spermatozoa resulting from adjacent mode of segregation. Our study provides further evidence of ICE on chromosome X, Y and 18 in ROB translocation carriers. Therefore, preimplantation genetic diagnosis (PGD) is recommended for ROB translocation carriers to minimize the risk of having an affected child or the distress of pregnancy termination, and to reduce the risk of miscarriage due to abnormal segregation of the translocation [31-34]. Since the proband is phenotypically normal with normal fertility, we considered the chromosomal rearrangement of the person to be a balanced polymorphism [35]. The aberration can provide material for evolution. The establishment of a new human subspecies with a diploid complement of 44 chromosomes could occur if a small population with the karyotype of the proband undergoes long-term reproductive isolation [36].