200: Sperm Sequencing Reveals Extensive Positive Selection in the Male Germline
Base by Base16 Nov 2025

200: Sperm Sequencing Reveals Extensive Positive Selection in the Male Germline

Music:
Enjoy the music based on this article at the end of the episode.

DOI:
10.1038/s41586-025-09448-3

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

On PaperCast Base by Base you’ll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

️ Episode:
200: 200: Sperm Sequencing Reveals Extensive Positive Selection in the Male Germline

️ Season:
1

Article title:
Sperm sequencing reveals extensive positive selection in the male germline

Journal:
Nature

QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2025-11-16.

QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited transcript sections describing (i) mutation rates in sperm vs blood, (ii) NanoSeq/duplex sequencing methodology and error correction, (iii) positive selection in the male germline including gene count and LOF/activating mechanisms, (iv) RAS–MAPK pathway involvement, (v) disease risk implications and paternal ag
- transcript topics: Sperm mutation rates and somatic comparison; NanoSeq/duplex sequencing methodology and error correction; Positive selection in the male germline: gene count and mutation mechanisms; Loss-of-function vs activating mutations and RAS–MAPK pathway; Disease risk implications and paternal age effects; Study limitations and boundaries of NanoSeq (variant types detected)

QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 7
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0

Metadata Audited:
- article_doi
- article_title
- article_journal
- license

Factual Items Audited:
- Baseline sperm mutation rate: 1.67 substitutions per year per haploid genome
- Sperm accumulate mutations ~8x slower than in blood
- Number of genes under significant positive selection: 40 (31 newly identified)
- Loss-of-function mutations are common among positively selected genes; many in the RAS–MAPK pathway
- Positive selection drives 2–3x increased risk of disease-causing mutations
- 3–5% of sperm from middle-aged to older individuals carry a pathogenic mutation across the exome

QC result: Pass.

Det här avsnittet är hämtat från ett öppet RSS-flöde och publiceras inte av Podme. Det kan innehålla reklam.

Avsnitt(462)

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

Yoon et al., Proceedings of the National Academy of Sciences - ANK3, which encodes the scaffolding protein ankyrin-G, is a major risk gene for bipolar disorder and schizophrenia, yet what it does in a...

24 Sep 24min

460: The lupus variant that also sharpens antiviral defense

460: The lupus variant that also sharpens antiviral defense

Virolainen et al., The American Journal of Human Genetics - A lupus signal on chromosome 11p15 narrows to a coding haplotype in IRF7 that most people in the world carry. This study shows the risk form...

21 Sep 24min

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

Arterbery et al., The American Journal of Human Genetics - Hundreds of genes have been reported as causes of cerebral palsy, yet there is no agreed model of what a pathogenic variant in a child with C...

13 Sep 24min

458: Somatic or inherited? Reading TP53 risk from shared DNA

458: Somatic or inherited? Reading TP53 risk from shared DNA

MacGregor et al., The American Journal of Human Genetics - Pathogenic TP53 variants found in blood have long been read as inherited Li-Fraumeni alleles, but many turn out to be somatic clones that gre...

10 Sep 25min

457: A deletion that raises Alzheimer risk, a duplication that lowers it

457: A deletion that raises Alzheimer risk, a duplication that lowers it

Quenez O et al., The American Journal of Human Genetics - Rare copy-number variants were called from 22,319 exomes covering early-onset Alzheimer disease, late-onset disease and unaffected controls, t...

9 Sep 24min

456: Beyond exons: where heritability hides as traits get more polygenic

456: Beyond exons: where heritability hides as traits get more polygenic

Fuhrer J et al., The American Journal of Human Genetics - Across 34 complex traits and disorders, a MiXeR-based framework partitions SNP heritability over 74 functional annotations and finds that exon...

8 Sep 45min

455: Agentic genomics: the bottleneck moves from code to judgment

455: Agentic genomics: the bottleneck moves from code to judgment

Corpas M et al., Cell Genomics - A Perspective arguing that autonomous AI agents which discover, configure and chain bioinformatics operations from natural-language instructions have shifted the bottl...

7 Sep 13min

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

Ali T et al., JCI Insight - Um antirretroviral aprovado para HIV, dado por via oral em microdose, prolongou a sobrevida de camundongos que carregam a proteína priônica humana e foram infectados com pr...

2 Sep 17min

Populärt inom Vetenskap

dumma-manniskor
p3-dystopia
rss-mottagningen
allt-du-velat-veta
angestpodden
kapitalet-en-podd-om-ekonomi
rss-ronden
det-morka-psyket
ufo-sverige
svd-nyhetsartiklar
4health-med-anna-sparre
sexet
rss-vetenskapsradion
rss-arkeologi-historia-podden-som-graver-i-vart-kulturlandskap
bildningspodden
rss-spraket
rss-vetenskapsradion-2
ideer-som-forandrar-varlden
rss-ufobortom-rimligt-tvivel
rss-geopodden-2