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Chromosome distribution in human sperm – a 3D multicolor banding-study



Nuclear architecture studies in human sperm are sparse. By now performed ones were practically all done on flattened nuclei. Thus, studies close at the in vivo state of sperm, i.e. on three-dimensionally conserved interphase cells, are lacking by now. Only the position of 14 chromosomes in human sperm was studied.


Here for the first time a combination of multicolor banding (MCB) and three-dimensional analysis of interphase cells was used to characterize the position and orientation of all human chromosomes in sperm cells of a healthy donor. The interphase nuclei of human sperm are organized in a non-random way, driven by the gene density and chromosome size.


Here we present the first comprehensive results on the nuclear architecture of normal human sperm. Future studies in this tissue type, e.g. also in male patients with unexplained fertility problems, may characterize yet unknown mechanisms of infertility.


Interphase chromosome organization and nuclear architecture are already being investigated for a long time [13]. Chromosomes have been demonstrated to be located in specific regions in the interphase nucleus. These were called 'chromosome territories' [47]. However, our own multicolor banding (MCB) based studies [8] showed, that the chromosome shape is not lost in the interphase nucleus and one can even identify interphase chromosomes instead of only chromosome territory [911]. MCB is the only approach available at present that provides the possibility of characterizing the chromosomal integrity of arbitrary interphase cell populations [12, 13]. It is still a matter of discussion what influences more the nuclear position of chromosomes: chromosome size or gene density. It has been repeatedly shown that small chromosomes preferentially locate close to the center of the nucleus, while large chromosomes can be found in the nuclear periphery of human fibroblasts [1115]. Nonetheless, also evidence for a gene density-correlated radial arrangement of chromosomes in the nucleus was provided [16]. Human chromosome #19, which is gene-dense and early replicating shows a localization in the central part, for the approximately same sized chromosome 18 a localization in the peripheral part of the nucleus was repeatedly proven. As the latter is gene-poorer and comprises late-replicating chromatin this gene-density factor is often discussed as a general principle, also as this nuclear topological arrangement was conserved during evolution [11, 619].

Three-dimensional (3D) FISH analysis became a major tool for studying the high order chromatin organization in the cell nucleus [20, 21]. However, up to now only one 3D-study is available for sperm [22]. In the present study the MCB-based [5] analysis on 3D preserved sperm was performed using suspension fluorescence in situ hybridization (S-FISH) [11, 23].

Results and discussion

MCB studies combined with S-FISH

Here we present the first genome-wide MCB-based study on 3D-preserved interphase nuclei derived from sperm (Fig. 1). Previously, comparable FISH-studies on sperm were performed on flattened nuclei with the known disadvantages of possible artifacts due to transformation of a spherical into a pancake-like object [11, 2426] or even on decondensed nuclei with DNA looping out [27, 28]. As for probes, the ones used were: whole, or arm-specific chromosome paintings, or centromeric probes [2329]. We are aware of only one previous 3D-study on human sperm done by confocal microscope [22].

Figure 1
figure 1

a) Scheme of a human sperm nucleus after DAPI-staining and how it presented in this study. The nucleus has a convexity where the sperm tail was attached at the cell. This convexity is shown here in exaggeration to make clear how the axial orientation of a nucleus was determined. As described in the text the sperm was divided into a central and a peripheral part, and deduced from that a head, middle and tail part could be defined. b) Examples for chromosomal positions in sperm: 1. chromosome 21 located in periphery and head of the sperm 2. chromosome 8 located in the center and head of the sperm. 3. X-chromosome located in periphery and middle of the sperm 4. chromosome 8 located in center and head of the sperm. 5. X-chromosome located in periphery and tail of the sperm. 6. X-chromosome located in center and tail of the sperm 7. chromosome 8 orientated axial 8. chromosome 10 orientated non-axial 9. chromosome 3 orientated linear 10. chromosome 11 orientated non-linear.

Position, orientation and configuration of individual chromosomes

As summarized in Figures 2, 3, 4, 5, 6, 7, 8, 9 and Table 1 the statistical analysis revealed correlations between the investigated parameters central/peripheral, head/middle/tail, axial/non-axial, linear/non-linear and orientation of the chromosomal arms towards the sperm head, when analyzing the chromosomes by groups (see below).

Figure 2
figure 2

Chromosomal distribution within the sperm cell evaluated according to the parameters 'central' (yellow) and 'peripheral' (red) localization (Fig. 1a). The chromosomes (= chr.#) are arranged from left to right corresponding to the probability of their whereabouts in a more peripheral or a more central way.

Figure 3
figure 3

Tree clustering algorithm of chromosomes localization on 'peripheral' and 'central' parts of the sperm deduced from the data of Fig. 2. The chromosome numbers in the X-axis are color-coded as shown in the legend on the right side of the diagram: A-group chromosomes in red, B-group in light-green, C-group in blue, D-group in violet, E-group in purple, F-group in dark-green, G-group in orange and gonosomes X and Y in gray.

Figure 4
figure 4

Distribution of the sperm chromosomes according to the parameters 'head' (yellow), 'tail' (red) and 'middle' (blue).

Figure 5
figure 5

Tree clustering algorithm of chromosomal localization according to 'middle' and 'tail and head'. The figure is composed as described in the legend for Fig. 3.

Figure 6
figure 6

Arrangement of sperm chromosomes according to the parameters 'non-axial' (yellow) and 'axial' (red).

Figure 7
figure 7

Chromosomal arrangement according to 'axial' and 'non-axial' in a clustering algorithm. The figure is composed as described in the legend for Fig. 3.

Figure 8
figure 8

Sperm chromosomes arranged according to the parameters 'non-linear' (yellow) and 'linear' (red).

Figure 9
figure 9

Chromosomal arrangement according to 'linear' and 'non-linear' in a clustering algorithm. The figure is composed as described in the legend for Fig. 3.

Table 1 Orientation of chromosomes in sperm

Position of chromosomal sub-groups A-G

The ISCN provides the subdivision of human chromosomes in sub-groups A through G [30]. This is based on the chromosomal shape, size and centromeric position. In Figs. 3, 5, 7 and 9 clusters were formed from the obtained data and correlated with these chromosomal sub-groups.

A- and B-group chromosomes are primarily located in the periphery (Fig. 3). While A-group is equally orientated towards the tail and head of the sperm, B-group is more frequently found in the middle and head part of the sperm (Fig. 5 and data not shown). These results are in concordance with previous studies for #1 [25, 29], #2 [25] and #5 [23]. According to [29] the chromosome 2 is located more towards the tail of the sperm, which we could confirm by MCB.

Chromosomes of the C-group are positioned basically in the middle of sperm (Fig. 5). As visible in Fig. 3 C-group is localized preferentially in the periphery. Exceptions are here according to Fig. 3 chromosomes #6 and #12. It has to be noticed that for chromosome 6 already different data was reported [29], i.e. that chromosome 6 was observed to behave like all other chromosomes of the C-group as detected here. This discrepancy might be due to the fact that Zalenkaya and Zalensky (2004) [29] did their study on swollen and flattened slides and in parts with centromeric probes. On the other hand they report similar data as we found for chromosome 7 [29]. So further studies are necessary for a better understanding of the nuclear position of chromosome 6.

The D-group chromosomes can all be found in the central part of the sperm nucleus (Fig. 3). Also all three of them belong to the cluster which whereabouts are in the middle of the sperm (Fig. 5). Nonetheless, it is obvious that a tendency towards head or tail localization increases starting from #15, over #14 to #13. Hazzouri and coworkers found comparable data for chromosome 13, previously [22].

The E-group chromosomes #16 and #17 are localized in between middle and head and more towards the center of the sperm, as previously found by [29]. Distribution of chromosome #18 essentially differs from other chromosomes of this group as this chromosome is of preference to find on periphery in tail or head of the sperm cell (Figs. 3 and 5), as previously reported by others [26].

The F-group chromosomes #19 and #20 can both mainly be found towards the sperm head (Fig. 5 and data not shown). However, for the distribution towards periphery and center chromosomes #19 (central position) and #20 (peripheral position) differ clearly from each other. A similar observation was the outcome of this study for the G-group chromosomes 21 (peripheral position) and 22 (central position). On the other hand, both G-group chromosomes are located in the middle of the sperm (Figs. 3 and 5).

Both gonosomes show a similar distribution, i.e. they are found in the periphery of the sperm. The X-chromosome is localized towards the middle and tail of the sperm (Fig. 5 and data not shown), while the Y-chromosome can be found in the middle part.

Orientation and configuration of chromosomal sub-groups A-G

All data concerning chromosomal orientation and configuration in sperm are summarized in Figs. 7 and 9 and Tab. 1.

Of the A-group chromosomes #1 and #3 tend to be localized more axial than #2. Surprisingly, the longest human chromosome #1 tends to be configured more linear rather than #2 and #3. Also the B-group chromosomes have a more linear configuration. #5 tends to be axial orientated, #4 non-axial.

The C-group is arranged in a non-axial way, in general. Chromosomes #7 and #8 are exceptions here. Chromosomes #6 to #9 tend to be more linear than the others of the C-group. D-group chromosomes turned out to be located non-axial. Chromosomes #13 and #15 are arranged non-linear, #14 more linear.

The E-group falls again in two different clusters: chromosomes #16 and #17 are configured non-axial and non-linear, while chromosome #18 behaves the other way round. The same holds true for the F-group: #19 is non-axial and non-linear, #20 axial and linear arranged. In G-group similar things is to substitute by the same, even though the difference in axial/non-axial is not that expressed. Chromosome #22's configuration is more linear that of #21.

The gonosomes again behave very similar in terms of a more linear and neither expressed axial or non-axial behaviour.

A prevalence in orientation of p- or q-arm towards the sperm head could not be observed for half of the chromosomes (Tab. 1). Possible tendencies were observed for chromosomes #4, #6, #8, #13, #16, #20, #22 (p-arm) and #3, #5, #11, #12 and #15 (q-arm). However, as these results were obtained on 3 to 22 nuclei with axial orientated cells, they have to be considered as preliminary.

Possible correlations with chromosome size

As summarized in Fig. 10 a direct correlation of position of the chromosomes (from center to periphery) with their size can be found for most of the chromosomes. Apart from 8 chromosomes (#1, #2, #6. #14, #18, #20, #21 and Y) all other closely adjoin to the straight line of regression according with their size. The correlation level is high (correlation coefficient = 0.952).

Figure 10
figure 10

Result of regression analysis for the correlation of chromosomal distribution [center/periphery (Y-axis)] and the chromosome (chr.) size in mega-base pair (mega-bp). The regression is shown as a red line. The chromosomes are marked as dots in the corresponding colors of the groups A to G and gonosomes (X, Y), as specified in Figure 3.

Possible correlations with gene density

When arranging the smaller sized chromosomes (groups E, F, G and Y chromosome) then the gene density seems to have a more significant influence on the positioning of chromosomes in sperm. No such observation was possible for the larger chromosomes (results not shown). In Fig. 11 the smaller sized chromosomes are closely adjoined to the straight line of regression but comparing with the size dependence distribution relation has the opposite value. Chromosomes with a higher gene density are located in the center. Therefore, the Correlation Coefficient has negative value and equal to -0.983. The correlation level is high, however, chromosomes #20 and #22 do not completely fit.

Figure 11
figure 11

Regression analysis for a similar correlation of small chromosomes F- to G-groups and Y chromosome as in Fig. 10. Here the chromosomal distribution [center/periphery (Y-axis)] are correlated with the gene density of each chromosome.


It could be demonstrated that MCB combined with S-FISH is a powerful tool for a three-dimensional analysis of chromosome position in sperm interphase nuclei. The topology in interphase nucleus of human is organized in a non-random way driven by chromosome size and gene density. This is now not only clear for lymphocytes but also for sperm. Interestingly for most of the chromosomes the distribution of the territories seem to be similar in sperm and lymphocytes [31] apart from the acrocentric chromosomes as previously discussed [11].

Further combined application of multicolor banding with three-dimensional analysis in various tissues will provide to a better understanding of interphase architecture in human. Future studies in sperm of patients with unexplained fertility problems may characterize yet unknown mechanisms of infertility, as Cremer and colleagues postulated in 2004 [32]: the nuclear architecture may be an integrated part of the epigenetic mechanisms.


Human sperm

Human sperm sample was collected in a sterile container after 3 days of sexual abstinence from a fertile, 30 year-old man with normal seminal parameters and normal karyotype. After liquefaction at room temperature, the samples was washed three times in 1 × phosphate-buffered saline by centrifugation (5 min at 2000 rpm) and fixed in fresh fixative (1:3 glacial acetic acid: methanol) [33].

Suspension-fluorescence in situ hybridization (S-FISH)

S-FISH on interphase sperm cells was done as previously reported [11]. 30 cells were evaluated per chromosome i.e. overall 720 interphase nuclei were analyzed. The same number of evaluated cells per chromosome was chosen in comparable previous studies [11, 29].


Analysis of chromosomal position in sperm included several parameters. The localization of chromosomes in periphery or center was determined. For that the sperm was divided into two spheres and 50% of the radius of cell was defined as central, the remainder as peripheral (Figs. 1, 2, 3). As the sperm axis can be determined in DAPI-staining (see [11] and Fig. 1a) it is also possible to define chromosomal localization as head, middle and tail parts of the sperm (Figs. 1; 4, 5). Moreover, it was determined if the chromosomes located along the longitudinal axis of the sperm or not. Chromosomes were defined as axial when the deviation was less the 45° and/or the chromosome was not entangled (Figs. 1; 6, 7). The latter was also registered by distinguishing linear and non-linear configuration of chromosomes (Figs. 1; 8, 9). Finally, the orientation concerning the short p- and long q-arms of sperm chromosomes towards the head of sperm was recorded (Fig. 1; Tab. 1).


Statistical analysis was performed using Student's t-test and One Way ANOVA (Analysis of Variance) to determine significant differences of chromosome's arrangement in sperm. Statistical significance was defined as p < 0.05.

Estimation of similarity in a position and orientations between various chromosomes was done with the application of cluster analysis (Figs. 3, 5, 7 and 9). The purpose of this algorithm is to correlate chromosomes within clusters, which are depicted as hierarchical trees. Linkage distances between chromosomes are computed based of Euclidean distances. This is simply the geometric distance in the multidimensional space. For analysis of dependence of chromosomes distribution on periphery and the center of sperm from the length and relative gene density of chromosomes, the regression analysis was used (Figs. 10, 11).


  1. Vogel F, Schroeder TM: The internal order of the interphase nucleus. Humangenetik 1974, 25: 265–292. 10.1007/BF00336904

    Article  CAS  PubMed  Google Scholar 

  2. Lima-de-Faria A, Mitelman F: The chromosome territory of human oncogenes. Biosci Rep 1996, 6: 349–354. 10.1007/BF01116421

    Article  Google Scholar 

  3. Zakian VA: Cell biology: Architecture of interphase nuclei. Nature 1984, 308: 406. 10.1038/308406a0

    Article  CAS  PubMed  Google Scholar 

  4. Cremer T, Cremer C: Chromosome territories, nuclear architecture and gene regulation in mammalian cells. Nat Rev Genet 2001, 2: 292–301. 10.1038/35066075

    Article  CAS  PubMed  Google Scholar 

  5. Williams RE, Fisher AG: Chromosomes, positions please! Nature Cell Biology 2003, 5: 388–390. 10.1038/ncb0503-388

    Article  CAS  PubMed  Google Scholar 

  6. Branco MR, Pombo A: Intermingling of chromosome territories in interphase suggests role in translocations and transcription dependent associations. PLoS Biol 2006, 4: e138. 10.1371/journal.pbio.0040138

    Article  PubMed Central  PubMed  Google Scholar 

  7. Chevret E, Volpi EV, Sheer D: Mini review: form and function in the human interphase chromosome. Cytogenet Cell Genet 2000, 90: 13–21. 10.1159/000015654

    Article  CAS  PubMed  Google Scholar 

  8. Weise A, Mrasek K, Fickelscher I, Claussen U, Cheung SW, Cai WW, Liehr T, Kosyakova N: Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set. J Histochem Cytochem 2008, 56: 487–493. 10.1369/jhc.2008.950550

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Weise A, Starke H, Heller A, Uwe C, Liehr T: Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis. Int J Mol Med 2002, 9: 359–361.

    CAS  PubMed  Google Scholar 

  10. Lemke J, Claussen J, Michel S, Chudoba I, Mühlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U: The DNA-based structure of human chromosome 5 in interphase. Am J Hum Genet 2002, 71: 1051–1059. 10.1086/344286

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  11. Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T: Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Mol Cytogenet 2008, 1: 9. 10.1186/1755-8166-1-9

    Article  PubMed Central  PubMed  Google Scholar 

  12. Iourov I, Liehr T, Vorsanova S, Kolotii A, Yurov Y: Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res 2006, 14: 223–229. 10.1007/s10577-006-1037-6

    Article  CAS  PubMed  Google Scholar 

  13. Yurov Y, Iourov I, Vorsanova S, Demidova I, Kravetz V, Beresheva A, Kolotii A, Monakchov V, Uranova N, Vostrikov V, Soloviev I, Liehr T: The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1. Schizophrenia Research 2008, 98: 139–147. 10.1016/j.schres.2007.07.035

    Article  PubMed  Google Scholar 

  14. Bolzer A, Kreth G, Solovei I, Koehler D, Saracoglu K, Fauth C, Muller S, Cremer C, Eils R, Speicher MR, Cremer T: Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes. PLoS Biol 2005, 3: e157. 10.1371/journal.pbio.0030157

    Article  PubMed Central  PubMed  Google Scholar 

  15. Sun HB, Shen J, Yokota H: Size-dependent positioning of human chromosomes in interphase nuclei. Biophys J 2000, 79(1):184–190.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  16. Croft JA, Bridger JM, Boyle S, Perry P, Teague P, Bickmore WA: Differences in the localization and morphology of chromosomes in the human nucleus. J Cell Biol 1999, 45: 1119–1131. 10.1083/jcb.145.6.1119

    Article  Google Scholar 

  17. Tanabe H, Müller S, Neusser M, von Hase J, Calcagno E, Cremer M, Solovei I, Cremer C, Cremer T: Evolutionary conservation of chromosome territory arrangements in cell nuclei from higher primates. Proc Natl Acad Sci USA 2002, 99: 4424–4429. 10.1073/pnas.072618599

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  18. Tanabe H, Küpper K, Ishida T, Neusser M, Mizusawa H: Inter- and intraspecific gene-density-correlated radial chromosome territory arrangements are conserved in old world monkeys. Cytogenet Genome Res 2005, 108: 255–261. 10.1159/000080824

    Article  CAS  PubMed  Google Scholar 

  19. McKenzie LJ, Carson SA, Marcelli S, Rooney E, Cisneros P, Torskey S, Buster J, Simpson JL, Bischoff FZ: Nuclear chromosomal localization in human preimplantation embryos: correlation with aneuploidy and embryo morphology. Hum Reprod 2004, 19: 2231–2237. 10.1093/humrep/deh391

    Article  PubMed  Google Scholar 

  20. Solovei I, Cavallo A, Schermelleh L, Jaunin F, Scasselati C, Cmarko D, Cremer C, Fakan S, Cremer T: Spatial preservation of nuclear chromatin architecture during three-dimensional fluorescence in situ hybridization (3D-FISH). Exp Cell Res 2002, 276: 10–23. 10.1006/excr.2002.5513

    Article  CAS  PubMed  Google Scholar 

  21. Cremer M, Hase J, Volm T, Brero A, Kreth G, Walter J, Fischer C, Solovei I, Cremer C, Cremer T: Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells. Chr Res 2001, 9: 541–567. 10.1023/A:1012495201697

    Article  CAS  Google Scholar 

  22. Hazzouri M, Rousseaux S, Mongelard F, Usson Y, Pelletier R, Faure AK, Vourc'h C, Sèle B: Genome organization in the human sperm nucleus studied by FISH and confocal microscopy. Mol Reprod Dev 2000, 55: 307–315. 10.1002/(SICI)1098-2795(200003)55:3<307::AID-MRD9>3.0.CO;2-P

    Article  CAS  PubMed  Google Scholar 

  23. Steinhaeuser U, Starke H, Nietzel A, Lindenau J, Ullmann P, Claussen U, Liehr T: Suspension S-FISH a new technique for interphase. J Histochem Cytochem 2002, 50: 1697–1698.

    Article  CAS  PubMed  Google Scholar 

  24. Iourov IY, Liehr T, Vorsanova SG, Yurov YB: Interphase chromosomespecific multicolor banding (ICS-MCB): A new tool for analysis of interphase chromosomes in their integrity. Biomol Eng 2007, 24: 415–417. 10.1016/j.bioeng.2007.05.003

    Article  CAS  PubMed  Google Scholar 

  25. Mudrak O, Tomilin N, Zalensky A: Chromosome architecture in the decondensing human sperm nucleus. J Cell Sci 2005, 118: 4541–4550. 10.1242/jcs.02581

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  26. Luetjens CM, Payne C, Schatten G: Non-random chromosome positioning in human sperm and sex chromosome anomalies following intracytoplasmic sperm injection. Lancet 1999, 353: 1240. 10.1016/S0140-6736(99)80059-2

    Article  CAS  PubMed  Google Scholar 

  27. Barone JG, De Lara J, Cummings KB, Ward WS: DNA organization in human spermatozoa. J Androl 1994, 15: 139–144.

    CAS  PubMed  Google Scholar 

  28. Haaf T, Ward DC: Higher order nuclear structure in mammalian sperm revealed by in situ hybridization and extended chromatin fibers. Exp Cell Res 1995, 219: 604–611. 10.1006/excr.1995.1270

    Article  CAS  PubMed  Google Scholar 

  29. Zalenskaya IA, Zalensky AO: Non-random positioning of chromosomes in human sperm nuclei. Chromosome Res 2004, 12: 163–173. 10.1023/B:CHRO.0000013166.04629.97

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  30. ISCN (2005): An International System for Human Cytogenetic Nomenclature. Edited by: Shaffer LG, Tommerup N. S Karger, Basel; 2005.

    Google Scholar 

  31. Weierich C, Brero A, Stein S, von Hase J, Cremer C, Cremer T, Solovei I: Three-dimensional arrangements of centromeres and telomeres in nuclei of human and murine lymphocytes. Chromosome Res 2003, 11: 485–502. 10.1023/A:1025016828544

    Article  CAS  PubMed  Google Scholar 

  32. Cremer T, Küpper K, Dietzel S, Fakan S: Higher order chromatin architecture in the cell nucleus: on the way from structure to function. Biol Cell 2004, 96: 555–567. 10.1016/j.biolcel.2004.07.002

    Article  CAS  PubMed  Google Scholar 

  33. Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F: Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Mol Hum Reprod 2007, 13: 751–756. 10.1093/molehr/gam048

    Article  CAS  PubMed  Google Scholar 

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This study was supported in parts by the DAAD (A0704616/Ref326), the Evangelische Studienwerk e.V. Villigst, the Ernst-Abbe-Stiftung, the IZKF Jena and the DFG (LI 820/9-1, 436 ARM 17/11/06, 436 RUS 17/88/06, LI 820/11-1, LI 820/13-1, LI 820/15-1, LI 820/21-1).

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Correspondence to Marina Manvelyan.

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Authors' contributions

MM, FH and SB did 3-D-FISH in human sperm. FP and SB provided and prepared the human sperm pellet. FH, KM and AW adapted the S-FISH protocol for MCB-probes. FP, AW, RA, IS, TL have been involved in drafting the manuscript and revising it critically for important intellectual content.

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Manvelyan, M., Hunstig, F., Bhatt, S. et al. Chromosome distribution in human sperm – a 3D multicolor banding-study. Mol Cytogenet 1, 25 (2008).

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