Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States of America.
Department of Dermatology, Peking University First Hospital, Beijing, China.
PLoS One. 2018 Jun 13;13(6):e0198011. doi: 10.1371/journal.pone.0198011. eCollection 2018.
Recent findings of mosaicism (DNA sequence variation) challenge the dogma that each person has a stable genetic constitution. Copy number variations, point mutations and chromosome abnormalities in normal or diseased tissues have been described. We studied normal skin mosaicism of a single nucleotide polymorphism (SNP) [rs1426654, p.Thr111Ala] in SLC24A5, an ion transporter gene. This SNP is unusual in that more than 90% of people of European descent have homozygous germline A/A alleles, while more than 90% of East Asians and Blacks have homozygous germline G/G alleles. We found mosaicism in neonatal foreskins as well as in 69% of nearly 600 skin surface scraping samples from 114 donors of different ages. Strikingly, donors with germline (buccal or blood) A/A, A/G or G/G genotypes had all three sequences (A/A, A/G or G/G) in the skin surface scrapings. SNP sequence differences extended within the epidermis in the vertical dimension from basal cell layer to the stratum corneum at the surface, as well as across the two-dimensions of the skin surface. Furthermore, repeated scrapings in the same location revealed variation in the sequences in the same individuals over time, adding a fourth dimension to this variation. We then used this mosaicism to track the movement of epidermal cells during normal differentiation and characterize the patterning of epidermal cells during terminal differentiation. In this coordinated proliferation model of epidermal differentiation, the skin surface is alternatively populated by synchronous, cycling of waves of cells, with each group having a different DNA sequence. These groups of cells abruptly flatten into large sheets at the surface providing patches of uniform SNP sequence. This four-dimensional mosaicism is a normal, previously unrecognized form of dynamic mosaicism in human skin.
最近的嵌合体(DNA 序列变异)发现挑战了每个人都具有稳定遗传构成的教条。已经描述了正常或患病组织中的拷贝数变异、点突变和染色体异常。我们研究了 SLC24A5 离子转运基因中单核苷酸多态性(SNP)[rs1426654,p.Thr111Ala]的正常皮肤嵌合体。该 SNP 不寻常之处在于,超过 90%的欧洲血统人群具有纯合的胚系 A/A 等位基因,而超过 90%的东亚人和黑人群体具有纯合的胚系 G/G 等位基因。我们在新生儿包皮中以及 114 名不同年龄供体的近 600 个皮肤表面刮取样本中的 69%中发现了嵌合体。引人注目的是,具有胚系(颊或血液)A/A、A/G 或 G/G 基因型的供体在皮肤表面刮取物中均具有三种序列(A/A、A/G 或 G/G)。SNP 序列差异在垂直方向上从基底层延伸到表皮表面的角质层,以及在皮肤表面的两个维度上延伸。此外,在同一位置反复刮取显示同一个体的序列随时间变化,为这种变化增加了第四个维度。然后,我们利用这种嵌合体来跟踪表皮细胞在正常分化过程中的运动,并描述表皮细胞在终末分化过程中的模式。在这种协调的表皮分化增殖模型中,皮肤表面交替地被同步的、周期性的细胞波群所占据,每个细胞群具有不同的 DNA 序列。这些细胞群突然在表面变平成大片,提供均匀 SNP 序列的斑块。这种四维嵌合体是人类皮肤中一种正常的、以前未被认识到的动态嵌合体形式。