TY - JOUR
T1 - Variant pnldc1, defective pirna processing, and azoospermia
AU - Nagirnaja, L.
AU - Morup, N.
AU - Nielsen, J. E.
AU - Stakaitis, R.
AU - Golubickaite, I.
AU - Oud, M. S.
AU - Winge, S. B.
AU - Carvalho, F.
AU - Aston, K. I.
AU - Khani, F.
AU - Van Der Heijden, G. W.
AU - Marques, C. J.
AU - Skakkebaek, N. E.
AU - De Meyts, E. Rajpert
AU - Schlegel, P. N.
AU - Jorgensen, N.
AU - Veltman, J. A.
AU - Lopes, A. M.
AU - Conrad, D. F.
AU - Almstrup, K.
N1 - Funding Information:
Supported by a grant from Innovation Fund Denmark (14-2013-4, to Dr. Almstrup), ReproUnion, grants from the National Institutes of Health (R01HD078641, to Drs. Aston and Conrad, and P50HD096723, to Dr. Conrad), a starting grant from Fundação para a Ciência e a Tecnologia (IF/01262/2014, to Dr. Lopes), a grant from the Netherlands Organization for Scientific Research (918-15-667, to Dr. Veltman), and a grant from the Wellcome Trust (209451, to Dr. Veltman) Disclosure forms provided by the authors are available with the full text of this article at NEJM.org.
Publisher Copyright:
© 2021 Massachussetts Medical Society. All rights reserved.
PY - 2021/8/19
Y1 - 2021/8/19
N2 - P-element-induced wimpy testis (PIWI)-interacting RNAs (piRNAs) are short (21 to 35 nucleotides in length) and noncoding and are found almost exclusively in germ cells, where they regulate aberrant expression of transposable elements and postmeiotic gene expression.Critical to the processing of piRNAs is the protein poly(A)-specific RNase-like domain containing 1 (PNLDC1), which trims their 3′ ends and, when disrupted in mice, causes azoospermia and male infertility.METHODS We performed exome sequencing on DNA samples from 924 men who had received a diagnosis of nonobstructive azoospermia.Testicular-biopsy samples were analyzed by means of histologic and immunohistochemical tests, in situ hybridization, reverse- transcriptase-quantitative-polymerase-chain-reaction assay, and small-RNA sequencing.RESULTS Four unrelated men of Middle Eastern descent who had nonobstructive azoospermia were found to carry mutations in PNLDC1: the first patient had a biallelic stop-gain mutation, p.R452Ter (rs200629089; minor allele frequency, 0.00004); the second, a novel biallelic missense variant, p.P84S; the third, two compound heterozygous mutations consisting of p.M259T (rs141903829; minor allele frequency, 0.0007) and p.L35PfsTer3 (rs754159168; minor allele frequency, 0.00004); and the fourth, a novel biallelic canonical splice acceptor site variant, c.607-2A→T.Testicular histologic findings consistently showed error-prone meiosis and spermatogenic arrest with round spermatids of type Sa as the most advanced population of germ cells.Gene and protein expression of PNLDC1, as well as the piRNA-processing proteins PIWIL1, PIWIL4, MYBL1, and TDRKH, were greatly diminished in cells of the testes.Furthermore, the length distribution of piRNAs and the number of pachytene piRNAs was significantly altered in men carrying PNLDC1 mutations.CONCLUSIONS Our results suggest a direct mechanistic effect of faulty piRNA processing on meiosis and spermatogenesis in men, ultimately leading to male infertility.(Funded by Innovation Fund Denmark and others.).
AB - P-element-induced wimpy testis (PIWI)-interacting RNAs (piRNAs) are short (21 to 35 nucleotides in length) and noncoding and are found almost exclusively in germ cells, where they regulate aberrant expression of transposable elements and postmeiotic gene expression.Critical to the processing of piRNAs is the protein poly(A)-specific RNase-like domain containing 1 (PNLDC1), which trims their 3′ ends and, when disrupted in mice, causes azoospermia and male infertility.METHODS We performed exome sequencing on DNA samples from 924 men who had received a diagnosis of nonobstructive azoospermia.Testicular-biopsy samples were analyzed by means of histologic and immunohistochemical tests, in situ hybridization, reverse- transcriptase-quantitative-polymerase-chain-reaction assay, and small-RNA sequencing.RESULTS Four unrelated men of Middle Eastern descent who had nonobstructive azoospermia were found to carry mutations in PNLDC1: the first patient had a biallelic stop-gain mutation, p.R452Ter (rs200629089; minor allele frequency, 0.00004); the second, a novel biallelic missense variant, p.P84S; the third, two compound heterozygous mutations consisting of p.M259T (rs141903829; minor allele frequency, 0.0007) and p.L35PfsTer3 (rs754159168; minor allele frequency, 0.00004); and the fourth, a novel biallelic canonical splice acceptor site variant, c.607-2A→T.Testicular histologic findings consistently showed error-prone meiosis and spermatogenic arrest with round spermatids of type Sa as the most advanced population of germ cells.Gene and protein expression of PNLDC1, as well as the piRNA-processing proteins PIWIL1, PIWIL4, MYBL1, and TDRKH, were greatly diminished in cells of the testes.Furthermore, the length distribution of piRNAs and the number of pachytene piRNAs was significantly altered in men carrying PNLDC1 mutations.CONCLUSIONS Our results suggest a direct mechanistic effect of faulty piRNA processing on meiosis and spermatogenesis in men, ultimately leading to male infertility.(Funded by Innovation Fund Denmark and others.).
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U2 - 10.1056/NEJMoa2028973
DO - 10.1056/NEJMoa2028973
M3 - Article
C2 - 34347949
AN - SCOPUS:85113319818
SN - 0028-4793
VL - 385
SP - 707
EP - 719
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 8
ER -