Evidence map›Paper›PMID 26017218›Full record

ArticlePloS one2015

Spag17 deficiency results in skeletal malformations and bone abnormalities.

Maria Eugenia Teves, Gobalakrishnan Sundaresan, David J Cohen, Sharon L Hyzy, Illya Kajan, Melissa Maczis, Zhibing Zhang, Richard M Costanzo, Jamal Zweit, Zvi Schwartz and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Novel loss-of-functionFrontiers in endocrinology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. SPAG17 mediates nuclear translocation of protamines during spermiogenesis.Frontiers in cell and developmental biology · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Intraflagellar Transport Proteins as Regulators of Primary Cilia Length.Frontiers in cell and developmental biology · 2021
    Review
  15. A novel hypomorphic allele ofDisease models & mechanisms · 2020
    Article
  16. Article
  17. Article
  18. Two Insertion/Deletion Variants withinAnimals : an open access journal from MDPI · 2019
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Maria Eugenia TevesDepartment of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Gobalakrishnan SundaresanDepartment of Radiology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
David J CohenDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Sharon L HyzyDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Illya KajanDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Melissa MaczisDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Zhibing ZhangDepartment of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, Virginia, United States of America; Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Richard M CostanzoDepartment of Physiology and Biophysics, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Jamal ZweitDepartment of Radiology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Zvi SchwartzDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Barbara D BoyanDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia, United States of America; Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Jerome F StraussDepartment of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, Virginia, United States of America; Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Virginia Commonwealth University · US

Funding

MOLECULAR BASIS OF MAMMALIAN SPERM MOTILITYR01HD037416 · NICHD · VIRGINIA COMMONWEALTH UNIVERSITY · PI STRAUSS, JEROME F · 2000 to 2010
$2.4M
Dissection of the Structural Basis of MEIG1 in Assembling Sperm FlagellaR01HD076257 · NICHD · WAYNE STATE UNIVERSITY · PI ZHANG, ZHIBING · 2013 to 2017
$1.5M
NICHD NIH HHS R01 HD037416NICHD NIH HHS R01 HD-076257NICHD NIH HHS R01 HD076257NICHD NIH HHS R01 HD-37416
6 · The paper itself

Abstract

Height is the result of many growth and development processes. Most of the genes associated with height are known to play a role in skeletal development. Single-nucleotide polymorphisms in the SPAG17 gene have been associated with human height. However, it is not clear how this gene influences linear growth. Here we show that a targeted mutation in Spag17 leads to skeletal malformations. Hind limb length in mutants was significantly shorter than in wild-type mice. Studies revealed differences in maturation of femur and tibia suggesting alterations in limb patterning. Morphometric studies showed increased bone formation evidenced by increased trabecular bone area and the ratio of bone area to total area, leading to reductions in the ratio of marrow area/total area in the femur. Micro-CTs and von Kossa staining demonstrated increased mineral in the femur. Moreover, osteocalcin and osterix were more highly expressed in mutant mice than in wild-type mice femurs. These data suggest that femur bone shortening may be due to premature ossification. On the other hand, tibias appear to be shorter due to a delay in cartilage and bone development. Morphometric studies showed reduction in growth plate and bone formation. These defects did not affect bone mineralization, although the volume of primary bone and levels of osteocalcin and osterix were higher. Other skeletal malformations were observed including fused sternebrae, reduced mineralization in the skull, medial and metacarpal phalanges. Primary cilia from chondrocytes, osteoblasts, and embryonic fibroblasts (MEFs) isolated from knockout mice were shorter and fewer cells had primary cilia in comparison to cells from wild-type mice. In addition, Spag17 knockdown in wild-type MEFs by Spag17 siRNA duplex reproduced the shorter primary cilia phenotype. Our findings disclosed unexpected functions for Spag17 in the regulation of skeletal growth and mineralization, perhaps because of its role in primary cilia of chondrocytes and osteoblasts.

Indexed as

AnimalsAnimals, NewbornBone and BonesCells, CulturedChondrocytesCiliaFemaleFemurMaleMice, Inbred C57BLMice, KnockoutMicrotubule ProteinsOsteoblastsSkullTibiaMicrotubule ProteinsSPAG17 protein, mouse

Identifiers

PMID26017218
PMCPMC4446355
OpenAlexW407253126

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.